Chemist Jobs in Rhode Island

- 38 Jobs
  • Quality Control Chemist

    Tedor Pharma Services 3.9company rating

    Chemist Job In Cumberland, RI

    Company Information: Tedor is a privately held pharmaceutical company a CDMO that develops drug product for both innovator and established companies. We are customer-focused oral solid dose CDMO with a strong track record of meeting aggressive development and commercialization timelines Over the past 20 years we have helped customers received many product approvals.We attribute this success to our company-wide focus on quality, customer service, and meeting timelines. Everything we do, and how we do it, is focused on helping our clients to achieve their product objectives. Position Summary: The role of the Quality Control Chemist is a vital role that is essential to manage and execute the quality testing that is required for drug substance on the commercial market. Quality Control Chemist will also be responsible for method validation and release & stability testing for clinical trial and commercial drug products; therefore, verifying all products and/or substances meet acceptable quality standards and that they are in accordance with the company's policies & procedures, FDA policies & procedures, and any applicable cGMP requirements. Additionally, ensuring compliance, accuracy, and timeliness of specified testing processes, environmental monitoring, data review, data analysis, and data trending of all raw materials, finished formulations, stability samples, client-based & company-based projects, method development, equipment calibrations/qualification and/or transfers, and cleaning study qualifications are all essential responsibilities. Quality Control Chemists are expected to collaborate with QC Analysts and Development Chemists while performing the QC Chemist position. This is a full-time, non-exempt position that includes a competitive salary, and strong benefits. The Quality Control Chemist will report Directly to the Quality Control Manager or Director. Position Description: Responsibilities Head the collaboration between QC and Developmental Chemists personnel but also cross department collaboration regarding drug product development, commercial operations, commercial manufacturing, Quality Assurance, and Analytical Development. Evaluation of QC laboratory operational execution and resources needed to preform tests. Generate, review and revise QC GMP documentation (SOPs, protocols, technical reports, specifications, etc.) as needed. Revise and manage technical transfer of methods from internal labs for raw material analysis, in-process testing, as well as API and Drug Product testing under supervision of the Director. Review and report all QC data and generate Certificates of Analysis. Monitor and trend QC data generated by internal and contract testing labs. Initiate ICH stability study protocols, execute and generate of interim reports. Manage, write, and review Out of Specification/Atypical results/Out of Trend investigations, deviations, and CAPAs. Investigate and troubleshoot method issues. Review relevant sections of regulatory filings. Monitor calibration schedule. Contact vendors. Schedule visits for PM/Calib and repairs. Assist vendors on site. Coordinate stability operation activities and ensure quality products and systems. Determine stability sample requirements, develop stability protocols and oversee execution of stability protocols. Monitor stability chambers and chart recorders on a daily basis to confirm environmental conditions for acceptance with established specifications. Prepare stability data graphs to estimate expiration dates and verify product shelf life. Evaluate stability trends and prepare reports. Equipment Qualification, including data integrity program. Position Type & Expected Hours of Work This is a full-time, non-exempt position requiring a minimum of 40 hours of work per week, Monday through Thursday and some in person Friday's.. Some responsibilities may require work outside of normal office hours. Work Environment Level 2: Office Environment and Laboratory Environment The work environment characteristics described here are representative of those a teammate encounters while performing the essential functions of this role and within the daily operations of a professional office environment. Reasonable accommodations may be made to enable employees with disabilities to perform essential functions. This job operates in a professional office environment, as well as the laboratory environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets, as well as standard laboratory equipment and instrumentation. An employee in this role will be exposed to standard hazards founds within a laboratory environment such as chemicals; bloodborne pathogens; fumes; select agents; confined spaces. Proper laboratory attire and safety gear such as protective eyewear; laboratory coat; appropriate gloves must be observed. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. This role requires standard physical demands within a standard office and laboratory environment where sustained periods of standing, sitting, or walking will be part of an employee's daily routine, whether they are at their desk or in the laboratory. While performing the duties of this role, an employee is regularly required to talk or hear; use hands or fingers to handle or feel; reach with arms; bend or stoop; climb stairs; crawl or crouch; kneel; push or pull; type on a keyboard; use a computer mouse. Lastly, an employee must be able to lift ten (10) pounds. Travel Limited travel is expected for this position. Required Education & Experience B.S. in Chemistry or Pharmaceutical Science, or other related discipline such as life sciences, drug product development. Five to Seven (3 - 5) years of work/laboratory experience in the pharmaceutical industry, Quality Control (QC). 3 + years of experience in a regulated manufacturing or QC laboratory environment of analytical methods for pharmaceutical products Experience in QC testing of pharmaceutical and/or biologic products in a GMP environment. Solid understanding of GMP compliance, Quality Control CMC requirements for ANDAs, and other regulatory filings Excellent interpersonal, verbal, and written communication skills Demonstrated collaborative skills and prior leadership roles or positions Comfortable in a fast-paced, small company environment, ability to adjust workload based upon changing priorities Technical knowledge Strong Microsoft Word, Excel, and Office skills Experience in contracting testing laboratories Preferred Experience & Experience BS in relevant life science, scientific, or engineering discipline Three to Five (3 - 5) years of work/laboratory experience in the pharmaceutical industry, Quality Control (QC). Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. All duties, responsibilities, and activities may be subject to change at any time with or without notice. EEO Statement: Tedor Pharma, Inc. is proud to be an Equal Employment Opportunity and Affirmative Action employer. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. We do not discriminated based upon race, religion, color, marital status, national origin, gender, sexual orientation, gender identity, gender expression, age, status as a protected veteran, ancestry, medical condition, pregnancy, genetic information, status as an individual with any mental and/or physical disabilities, or any other status protected under federal, state, or local law.
    $63k-80k yearly est. 3d ago
  • Formulations Technician

    Lancesoft, Inc. 4.5company rating

    Chemist Job In North Kingstown, RI

    Day Shift: 8 AM - 5 PM 3 -5 non-negotiable requirements Lab experience (Formulating buffers/ reagents) Detailed-oriented Ability to multi-task Job Posting Description Activity in formulating large volumes of various reagents, coordination of the aliquot and testing of the reagents to ensure the quality of the final components. Perform Microarray testing and data analysis for Microarray Wash buffers May perform FiSH testing and analysis Work with team to ensure lean manufacturing principles are implemented and sustained Other duties included the writing, maintenance and reviewing of ISO compliant work instructions (WI) and standard operating procedures (SOP
    $58k-86k yearly est. 2d ago
  • Formulation Chemist

    Dexian

    Chemist Job In North Kingstown, RI

    Job Title: Formulations Technician/Laboratory Technician/Chemical Technician Duration: 06-12 Month(s) Pay Range: $15/Hr. - $22/hr. on W2 (without any benefits) Desired Experience: Can you please share the day in the life and responsibilities? Normal day will be working at a preparation station, typically in a self directed fashion to prepare solutions of chemical standards. This will require the use of fine motor skills, chemical handling knowledge, and use of a balance. Attention to detail and computer skills will be key in this area. Requirements will also be to aid in other areas of the building which can include product kitting, chemical waste disposal and unitizing/bulk filling operations, as well as cycle counting. What would be the hours for day shift? Typical works days start around 7 or 730 and run 4-430 depending on start time. This is a M-F shift. What type of analytical testing methods are used? Methods that will be used by this person will be direct weighing of chemicals [0.5 milligrams to kg level quantities]. Also, some unitizing equipment could be used including pumps and mixing devices. Adherence to our quality system is key for these. What type of automation (machines) methods are used. Methods that will be used by this person will be direct weighing of chemicals [0.5 milligrams to kg level quantities]. Also, some unitizing equipment could be used including pumps and mixing devices. Computers and laboratory information systems are also key to our operations. What type of products/materials are being tested? Various chemical solvents, and solids will be handled. These range from both organic and inorganic in nature. What type of experience are you looking for on a resume? ON the resume, typically experience with chemicals is highly preferred. Also use with an analytical balance is good. Typically, this is found from many environmental labs in the sample preparation departments. Please update the job description below to include details about your specific role. In compliance with Standard Operating Procedures, cGMP guidelines and all regulatory standards, performs, interprets, troubleshoots and documents laboratory tests and procedures in a production environment, including a wide variety of analytical weighing and formulation techniques. Able to work well in a team environment as well as independently. Performs calibration on production equipment including balances. Documents test results/procedures/processes. May write experiment reports, summaries and protocols. Job Qualifications Please update the minimum qualifications below to reflect the requirements for your specific role. May require some higher education or specialized training/certification, or equivalent combination of education and experience. No prior experience required. Dexian is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. As one of the largest IT staffing companies and the 2nd largest minority-owned staffing company in the U.S., Dexian was formed in 2023 through the merger of DISYS and Signature Consultants. Combining the best elements of its core companies, Dexian's platform connects talent, technology, and organizations to produce game-changing results that help everyone achieve their ambitions and goals. Dexian's brands include Dexian DISYS, Dexian Signature Consultants, Dexian Government Solutions, Dexian Talent Development and Dexian IT Solutions. Visit ******************* to learn more. Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status.
    $15 hourly 2d ago
  • R&D Chemist

    Fujifilm 4.5company rating

    Chemist Job In North Kingstown, RI

    FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our North Kingstown, RI facility for an R&D Chemist! With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process. The Role The successful candidate will lead the development and optimization of new platforms for photoimageable dielectric materials. This role involves collaboration with central R&D and product technology teams to drive raw material selection and formulation improvements. The ideal candidate will have a strong background in polymer synthesis and organic chemistry, with expertise in design, synthesis, and characterization of new materials. Additionally, the R&D Chemist will apply experimental design, problem-solving skills, and root cause analysis to innovate and enhance product performance, while providing support in troubleshooting material-related issues. Company Overview FUJIFILM Electronic Materials, U.S.A., Inc. is a wholly owned subsidiary of FUJIFILM Holdings America Corporation. FUJIFILM Electronic Materials, U.S.A., Inc. supplies the world's top semiconductor manufacturers with a broad array of products and services, including chemicals and advanced materials. The company's broad product portfolio includes high-purity acids/bases, photoresists, thin film formation materials, formulated products, CMP slurries, and polyimides for advanced packaging. The company has six state-of-the-art manufacturing facilities and research labs in the U.S., including Arizona, California, Colorado, Rhode Island, and Texas. For more information, please visit: ************************************** FUJIFILM Corporation is a subsidiary of FUJIFILM Holdings Corporation. FUJIFILM Holdings Corporation, headquartered in Tokyo, leverages its depth of knowledge and proprietary core technologies to deliver innovative products and services across the globe through the four key business segments of healthcare, electronics, business innovation, and imaging with over 70,000 employees. Guided and united by our Group Purpose of “giving our world more smiles,” we address social challenges and create a positive impact on society through our products, services, and business operations. Under its medium-term management plan, VISION2030, which ends in FY2030, we aspire to continue our evolution into a company that creates value and smiles for various stakeholders as a collection of global leading businesses and achieve a global revenue of 4 trillion yen (29 billion USD at an exchange rate of 140 JPY/USD). For more information, please visit: ************************* For further details about our commitment to sustainability and Fujifilm's Sustainable Value Plan 2030, click here. Job Description Key responsibilities for this role include: Lead the design and development of new platforms for photoimageable dielectric materials, contributing to innovative advancements in the industry. Drive the selection of new raw materials by collaborating closely with the central division R&D and product technology teams, supporting the design, synthesis, and characterization of novel materials. Optimize product formulations by integrating new raw materials, performance criteria, and customer requirements to achieve superior product outcomes. Utilize in-depth knowledge of polymer synthesis and organic chemistry to develop new polymer platforms and raw materials, including designing structures, developing synthetic routes, and characterizing the developed materials. Apply expertise in the design of experiments, problem-solving methods, and root cause analysis to innovate and improve processes and products. Provide support in troubleshooting material-related issues, ensuring efficient resolution and continuous improvement. REQUIREMENTS Bachelor's degree in Chemistry, Chemical Engineering, Materials Science, or a related field. Master's or PhD in Chemistry strongly preferred. 3-5 years of experience in organic chemistry, polymer synthesis, or related fields Experience in semiconductor lithography or related fields strongly preferred. Strong background in the design, development, and characterization of new materials. Hands-on experience with product formulation and raw material selection. Extensive knowledge of polymer synthesis and organic chemistry principles. Proficiency in designing synthetic routes and characterizing developed materials. Expertise in the design of experiments (DOE) and statistical analysis. Proven ability to apply problem-solving methods and conduct root cause analysis. Familiarity with material characterization techniques and instrumentation. Must have excellent capability to use PowerPoint, Excel, or other software tools to generate first-class presentations. Strong analytical and critical thinking skills. Excellent communication and collaboration abilities. Ability to work effectively in cross-functional teams. High level of self-motivation and initiative. Strong project management and organizational skills. MENTAL & EMOTIONAL REQUIREMENTS Resilience - Adapting well in the face of workplace stressors, the ability to work effectively and efficiently in high stress and conflict situations, the ability to remain poised under all circumstances, the ability to maintain regular attendance and be punctual. Communication - The ability to successfully and professionally express and exchange ideas and meanings with all levels of employees in the organization, the ability to interact appropriately with a variety of individuals including customers/clients, the ability to work as an integral part of a team, ability to interact effectively with people in a positive manner that engenders confidence and trust. Reasoning and decision-making - The ability to understand, remember and follow verbal and written instructions, the ability to reason logically and make sound decisions. Comprehension - The ability to complete tasks without direct supervision, the ability to simultaneously address multiple complete problems. Organizational skills - Ability to multitask without loss of efficiency or accuracy, the ability to work and sustain attention with distractions and interruptions, the ability to perform in situations requiring speed, deadlines or productivity quotas. To all agencies: Please, no phone calls or emails to any employee of Fujifilm about this requisition. All resumes submitted by search firms/employment agencies to any employee at Fujifilm via-email, the internet or in any form and/or method will be deemed the sole property of Fujifilm, unless such search firms/employment agencies were engaged by Fujifilm for this requisition and a valid agreement with Fujifilm is in place. In the event a candidate who was submitted outside of the Fujifilm agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (********************************).
    $105k-136k yearly est. 35d ago
  • R&D Chemist

    Fujifilm Diosynth Biotechnologies 4.0company rating

    Chemist Job In North Kingstown, RI

    FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our North Kingstown, RI facility for an R&D Chemist! With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process. The Role The successful candidate will lead the development and optimization of new platforms for photoimageable dielectric materials. This role involves collaboration with central R&D and product technology teams to drive raw material selection and formulation improvements. The ideal candidate will have a strong background in polymer synthesis and organic chemistry, with expertise in design, synthesis, and characterization of new materials. Additionally, the R&D Chemist will apply experimental design, problem-solving skills, and root cause analysis to innovate and enhance product performance, while providing support in troubleshooting material-related issues. Company Overview FUJIFILM Electronic Materials, U.S.A., Inc. is a wholly owned subsidiary of FUJIFILM Holdings America Corporation. FUJIFILM Electronic Materials, U.S.A., Inc. supplies the world's top semiconductor manufacturers with a broad array of products and services, including chemicals and advanced materials. The company's broad product portfolio includes high-purity acids/bases, photoresists, thin film formation materials, formulated products, CMP slurries, and polyimides for advanced packaging. The company has six state-of-the-art manufacturing facilities and research labs in the U.S., including Arizona, California, Colorado, Rhode Island, and Texas. For more information, please visit: ********************************************** Corporation is a subsidiary of FUJIFILM Holdings Corporation. FUJIFILM Holdings Corporation, headquartered in Tokyo, leverages its depth of knowledge and proprietary core technologies to deliver innovative products and services across the globe through the four key business segments of healthcare, electronics, business innovation, and imaging with over 70,000 employees. Guided and united by our Group Purpose of "giving our world more smiles," we address social challenges and create a positive impact on society through our products, services, and business operations. Under its medium-term management plan, VISION2030, which ends in FY2030, we aspire to continue our evolution into a company that creates value and smiles for various stakeholders as a collection of global leading businesses and achieve a global revenue of 4 trillion yen (29 billion USD at an exchange rate of 140 JPY/USD). For more information, please visit: ************************* For further details about our commitment to sustainability and Fujifilm's Sustainable Value Plan 2030, click here. Job Description Key responsibilities for this role include: * Lead the design and development of new platforms for photoimageable dielectric materials, contributing to innovative advancements in the industry. * Drive the selection of new raw materials by collaborating closely with the central division R&D and product technology teams, supporting the design, synthesis, and characterization of novel materials. * Optimize product formulations by integrating new raw materials, performance criteria, and customer requirements to achieve superior product outcomes. * Utilize in-depth knowledge of polymer synthesis and organic chemistry to develop new polymer platforms and raw materials, including designing structures, developing synthetic routes, and characterizing the developed materials. * Apply expertise in the design of experiments, problem-solving methods, and root cause analysis to innovate and improve processes and products. * Provide support in troubleshooting material-related issues, ensuring efficient resolution and continuous improvement. REQUIREMENTS * Bachelor's degree in Chemistry, Chemical Engineering, Materials Science, or a related field. Master's or PhD in Chemistry strongly preferred. * 3-5 years of experience in organic chemistry, polymer synthesis, or related fields * Experience in semiconductor lithography or related fields strongly preferred. * Strong background in the design, development, and characterization of new materials. * Hands-on experience with product formulation and raw material selection. * Extensive knowledge of polymer synthesis and organic chemistry principles. * Proficiency in designing synthetic routes and characterizing developed materials. * Expertise in the design of experiments (DOE) and statistical analysis. * Proven ability to apply problem-solving methods and conduct root cause analysis. * Familiarity with material characterization techniques and instrumentation. * Must have excellent capability to use PowerPoint, Excel, or other software tools to generate first-class presentations. * Strong analytical and critical thinking skills. * Excellent communication and collaboration abilities. * Ability to work effectively in cross-functional teams. * High level of self-motivation and initiative. * Strong project management and organizational skills. MENTAL & EMOTIONAL REQUIREMENTS * Resilience - Adapting well in the face of workplace stressors, the ability to work effectively and efficiently in high stress and conflict situations, the ability to remain poised under all circumstances, the ability to maintain regular attendance and be punctual. * Communication - The ability to successfully and professionally express and exchange ideas and meanings with all levels of employees in the organization, the ability to interact appropriately with a variety of individuals including customers/clients, the ability to work as an integral part of a team, ability to interact effectively with people in a positive manner that engenders confidence and trust. * Reasoning and decision-making - The ability to understand, remember and follow verbal and written instructions, the ability to reason logically and make sound decisions. * Comprehension - The ability to complete tasks without direct supervision, the ability to simultaneously address multiple complete problems. * Organizational skills - Ability to multitask without loss of efficiency or accuracy, the ability to work and sustain attention with distractions and interruptions, the ability to perform in situations requiring speed, deadlines or productivity quotas. To all agencies: Please, no phone calls or emails to any employee of Fujifilm about this requisition. All resumes submitted by search firms/employment agencies to any employee at Fujifilm via-email, the internet or in any form and/or method will be deemed the sole property of Fujifilm, unless such search firms/employment agencies were engaged by Fujifilm for this requisition and a valid agreement with Fujifilm is in place. In the event a candidate who was submitted outside of the Fujifilm agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (********************************).
    $96k-117k yearly est. 40d ago
  • R&D Chemist

    Fujifilm Holdings America 4.1company rating

    Chemist Job In North Kingstown, RI

    FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our North Kingstown, RI facility for an R&D Chemist! With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process. The Role The successful candidate will lead the development and optimization of new platforms for photoimageable dielectric materials. This role involves collaboration with central R&D and product technology teams to drive raw material selection and formulation improvements. The ideal candidate will have a strong background in polymer synthesis and organic chemistry, with expertise in design, synthesis, and characterization of new materials. Additionally, the R&D Chemist will apply experimental design, problem-solving skills, and root cause analysis to innovate and enhance product performance, while providing support in troubleshooting material-related issues. Company Overview FUJIFILM Electronic Materials, U.S.A., Inc. is a wholly owned subsidiary of FUJIFILM Holdings America Corporation. FUJIFILM Electronic Materials, U.S.A., Inc. supplies the world's top semiconductor manufacturers with a broad array of products and services, including chemicals and advanced materials. The company's broad product portfolio includes high-purity acids/bases, photoresists, thin film formation materials, formulated products, CMP slurries, and polyimides for advanced packaging. The company has six state-of-the-art manufacturing facilities and research labs in the U.S., including Arizona, California, Colorado, Rhode Island, and Texas. For more information, please visit: ************************************** FUJIFILM Corporation is a subsidiary of FUJIFILM Holdings Corporation. FUJIFILM Holdings Corporation, headquartered in Tokyo, leverages its depth of knowledge and proprietary core technologies to deliver innovative products and services across the globe through the four key business segments of healthcare, electronics, business innovation, and imaging with over 70,000 employees. Guided and united by our Group Purpose of “giving our world more smiles,” we address social challenges and create a positive impact on society through our products, services, and business operations. Under its medium-term management plan, VISION2030, which ends in FY2030, we aspire to continue our evolution into a company that creates value and smiles for various stakeholders as a collection of global leading businesses and achieve a global revenue of 4 trillion yen (29 billion USD at an exchange rate of 140 JPY/USD). For more information, please visit: ************************* For further details about our commitment to sustainability and Fujifilm's Sustainable Value Plan 2030, click here. Job Description Key responsibilities for this role include: Lead the design and development of new platforms for photoimageable dielectric materials, contributing to innovative advancements in the industry. Drive the selection of new raw materials by collaborating closely with the central division R&D and product technology teams, supporting the design, synthesis, and characterization of novel materials. Optimize product formulations by integrating new raw materials, performance criteria, and customer requirements to achieve superior product outcomes. Utilize in-depth knowledge of polymer synthesis and organic chemistry to develop new polymer platforms and raw materials, including designing structures, developing synthetic routes, and characterizing the developed materials. Apply expertise in the design of experiments, problem-solving methods, and root cause analysis to innovate and improve processes and products. Provide support in troubleshooting material-related issues, ensuring efficient resolution and continuous improvement. REQUIREMENTS Bachelor's degree in Chemistry, Chemical Engineering, Materials Science, or a related field. Master's or PhD in Chemistry strongly preferred. 3-5 years of experience in organic chemistry, polymer synthesis, or related fields Experience in semiconductor lithography or related fields strongly preferred. Strong background in the design, development, and characterization of new materials. Hands-on experience with product formulation and raw material selection. Extensive knowledge of polymer synthesis and organic chemistry principles. Proficiency in designing synthetic routes and characterizing developed materials. Expertise in the design of experiments (DOE) and statistical analysis. Proven ability to apply problem-solving methods and conduct root cause analysis. Familiarity with material characterization techniques and instrumentation. Must have excellent capability to use PowerPoint, Excel, or other software tools to generate first-class presentations. Strong analytical and critical thinking skills. Excellent communication and collaboration abilities. Ability to work effectively in cross-functional teams. High level of self-motivation and initiative. Strong project management and organizational skills. MENTAL & EMOTIONAL REQUIREMENTS Resilience - Adapting well in the face of workplace stressors, the ability to work effectively and efficiently in high stress and conflict situations, the ability to remain poised under all circumstances, the ability to maintain regular attendance and be punctual. Communication - The ability to successfully and professionally express and exchange ideas and meanings with all levels of employees in the organization, the ability to interact appropriately with a variety of individuals including customers/clients, the ability to work as an integral part of a team, ability to interact effectively with people in a positive manner that engenders confidence and trust. Reasoning and decision-making - The ability to understand, remember and follow verbal and written instructions, the ability to reason logically and make sound decisions. Comprehension - The ability to complete tasks without direct supervision, the ability to simultaneously address multiple complete problems. Organizational skills - Ability to multitask without loss of efficiency or accuracy, the ability to work and sustain attention with distractions and interruptions, the ability to perform in situations requiring speed, deadlines or productivity quotas. To all agencies: Please, no phone calls or emails to any employee of Fujifilm about this requisition. All resumes submitted by search firms/employment agencies to any employee at Fujifilm via-email, the internet or in any form and/or method will be deemed the sole property of Fujifilm, unless such search firms/employment agencies were engaged by Fujifilm for this requisition and a valid agreement with Fujifilm is in place. In the event a candidate who was submitted outside of the Fujifilm agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (********************************).
    $67k-101k yearly est. 31d ago
  • R&D Chemist

    Job Listingsfujifilm

    Chemist Job In North Kingstown, RI

    FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our North Kingstown, RI facility for an R&D Chemist! With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process. The Role The successful candidate will lead the development and optimization of new platforms for photoimageable dielectric materials. This role involves collaboration with central R&D and product technology teams to drive raw material selection and formulation improvements. The ideal candidate will have a strong background in polymer synthesis and organic chemistry, with expertise in design, synthesis, and characterization of new materials. Additionally, the R&D Chemist will apply experimental design, problem-solving skills, and root cause analysis to innovate and enhance product performance, while providing support in troubleshooting material-related issues. Company Overview FUJIFILM Electronic Materials, U.S.A., Inc. is a wholly owned subsidiary of FUJIFILM Holdings America Corporation. FUJIFILM Electronic Materials, U.S.A., Inc. supplies the world's top semiconductor manufacturers with a broad array of products and services, including chemicals and advanced materials. The company's broad product portfolio includes high-purity acids/bases, photoresists, thin film formation materials, formulated products, CMP slurries, and polyimides for advanced packaging. The company has six state-of-the-art manufacturing facilities and research labs in the U.S., including Arizona, California, Colorado, Rhode Island, and Texas. For more information, please visit: ************************************** FUJIFILM Corporation is a subsidiary of FUJIFILM Holdings Corporation. FUJIFILM Holdings Corporation, headquartered in Tokyo, leverages its depth of knowledge and proprietary core technologies to deliver innovative products and services across the globe through the four key business segments of healthcare, electronics, business innovation, and imaging with over 70,000 employees. Guided and united by our Group Purpose of “giving our world more smiles,” we address social challenges and create a positive impact on society through our products, services, and business operations. Under its medium-term management plan, VISION2030, which ends in FY2030, we aspire to continue our evolution into a company that creates value and smiles for various stakeholders as a collection of global leading businesses and achieve a global revenue of 4 trillion yen (29 billion USD at an exchange rate of 140 JPY/USD). For more information, please visit: ************************* For further details about our commitment to sustainability and Fujifilm's Sustainable Value Plan 2030, click here. Job Description Key responsibilities for this role include: Lead the design and development of new platforms for photoimageable dielectric materials, contributing to innovative advancements in the industry. Drive the selection of new raw materials by collaborating closely with the central division R&D and product technology teams, supporting the design, synthesis, and characterization of novel materials. Optimize product formulations by integrating new raw materials, performance criteria, and customer requirements to achieve superior product outcomes. Utilize in-depth knowledge of polymer synthesis and organic chemistry to develop new polymer platforms and raw materials, including designing structures, developing synthetic routes, and characterizing the developed materials. Apply expertise in the design of experiments, problem-solving methods, and root cause analysis to innovate and improve processes and products. Provide support in troubleshooting material-related issues, ensuring efficient resolution and continuous improvement. REQUIREMENTS Bachelor's degree in Chemistry, Chemical Engineering, Materials Science, or a related field. Master's or PhD in Chemistry strongly preferred. 3-5 years of experience in organic chemistry, polymer synthesis, or related fields Experience in semiconductor lithography or related fields strongly preferred. Strong background in the design, development, and characterization of new materials. Hands-on experience with product formulation and raw material selection. Extensive knowledge of polymer synthesis and organic chemistry principles. Proficiency in designing synthetic routes and characterizing developed materials. Expertise in the design of experiments (DOE) and statistical analysis. Proven ability to apply problem-solving methods and conduct root cause analysis. Familiarity with material characterization techniques and instrumentation. Must have excellent capability to use PowerPoint, Excel, or other software tools to generate first-class presentations. Strong analytical and critical thinking skills. Excellent communication and collaboration abilities. Ability to work effectively in cross-functional teams. High level of self-motivation and initiative. Strong project management and organizational skills. MENTAL & EMOTIONAL REQUIREMENTS Resilience - Adapting well in the face of workplace stressors, the ability to work effectively and efficiently in high stress and conflict situations, the ability to remain poised under all circumstances, the ability to maintain regular attendance and be punctual. Communication - The ability to successfully and professionally express and exchange ideas and meanings with all levels of employees in the organization, the ability to interact appropriately with a variety of individuals including customers/clients, the ability to work as an integral part of a team, ability to interact effectively with people in a positive manner that engenders confidence and trust. Reasoning and decision-making - The ability to understand, remember and follow verbal and written instructions, the ability to reason logically and make sound decisions. Comprehension - The ability to complete tasks without direct supervision, the ability to simultaneously address multiple complete problems. Organizational skills - Ability to multitask without loss of efficiency or accuracy, the ability to work and sustain attention with distractions and interruptions, the ability to perform in situations requiring speed, deadlines or productivity quotas. To all agencies: Please, no phone calls or emails to any employee of Fujifilm about this requisition. All resumes submitted by search firms/employment agencies to any employee at Fujifilm via-email, the internet or in any form and/or method will be deemed the sole property of Fujifilm, unless such search firms/employment agencies were engaged by Fujifilm for this requisition and a valid agreement with Fujifilm is in place. In the event a candidate who was submitted outside of the Fujifilm agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (********************************).
    $69k-105k yearly est. 33d ago
  • Chemist

    Actalent

    Chemist Job In Providence, RI

    We are seeking a dedicated Chemist to join our dynamic team. This role involves following permit requirements to collect and test compounds and samples using applied methods and techniques while adhering to company policies. You will be responsible for entering quantities, volumes, and analytical results into our waste management software (WMS/Preview), assisting with QA/QC analytical screening parameters as dictated by permits, and following all approved Laboratory SOPs. Ensuring compliance with environmental health and safety standards, including the proper handling, storage, and disposal of chemical agents, is essential. Additionally, you will assist in operating and maintaining laboratory equipment. Responsibilities * Collect and test compounds and samples per permit requirements. * Enter quantities, volumes, and analytical results into waste management software (WMS/Preview). * Assist with QA/QC analytical screening parameters. * Follow all approved Laboratory SOPs. * Ensure compliance with environmental health and safety standards, including proper handling, storage, and disposal of chemical agents. * Assist in operating and maintaining laboratory equipment. Essential Skills * Bachelor's degree in sciences (no experience required) * Associate degree in science with some laboratory experience * High School Diploma with at least one year of industry or academic laboratory experience * Proficiency in Excel and Word * Strong communication and written skills * Ability to stand for long periods * Capability to work in a fast-paced environment handling 100+ samples daily Additional Skills & Qualifications * Experience with pipetting, distillation, data analysis, pH testing, quality control, chemical handling, and wastewater treatment * Knowledge of Laboratory SOPs * Familiarity with WMS/Preview waste management system Work Environment You will be working with a growing team of 10 technicians within a fast-paced laboratory environment. The work schedule is Monday to Friday, 9 am to 5 pm, and the dress code is business casual with close-toed shoes. Personal protective equipment (PPE) will be provided on-site. The company culture emphasizes growth and internal advancement, with numerous opportunities to develop your career within the organization. There is a robust training program designed to help you gain valuable industry laboratory experience and exposure to SOPs and chemical testing. If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com. Pay and Benefits The pay range for this position is $22.00 - $22.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Providence,RI. Application Deadline This position is anticipated to close on Apr 4, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
    $22-22 hourly 10d ago
  • Client Registration/H.I. Tech for our Post Rd Office

    Thrive Behavioral Health Inc. 4.1company rating

    Chemist Job In Warwick, RI

    Do you want to make a positive difference in the lives of people that are challenged with mental illness and substance use disorders? Do you want to join a high-performing team of dedicated professionals who work effectively together, have fun, and share the joy of truly making the word a better place? Through the dedication and commitment of our staff, Thrive's clients receive the highest quality of care available, incorporating proven, effective treatment for substance use and mental health disorders. The ideal candidate will be results-driven, team-and detail-oriented professional who is comfortable working on multiple tasks in a deadline-oriented environment. Responsibilities: Meet with clients to data enter client registration information and conduct client orientation prior to the initial assessment. Obtain all necessary documents for enrollment as a Thrive Organization client and prepare clinical record. Review assessments, treatment plans, and discharges for completeness, conduct EHR audits as assigned, and maintain computerized client database. Process all requests and inquires for client information and release information in accordance with all federal and state laws as well as Organization policies, standards and procedures. Stay current on rules and regulations related to privacy, security, and recordkeeping practices. Respond to questions regarding confidentiality and release of information. Prepare records subpoenaed in accordance with Organization protocols. Process transcribed reports from the vendor in accordance with the Department's Standards and Procedures. Retrieve client records for appointments and audit per Organization procedure. Maintain sign-out system of records and re-file client records as necessary. Accurately file or scan client information in accordance with established systems. Identify duplicate records and merge when identified according to procedure with 100% accuracy. Refile client records as necessary and in accordance with established systems. Assist in review and audit procedures conducted by the HI/QI Department. Assist in the completion of various department projects. Review e-mail account daily for new messages. Requirements: High school graduate with one year secretarial/office certification program Two years' experience in a computerized medical or behavioral health office environment Benefits: Thrive Behavioral Health provides a friendly/family working environment, whose values include Dignity, Respect, Teamwork and Professional Support and Development. Thrive offers generous benefits after 30 days, PTO, paid holidays, your birthday off, and a 401k plan. ****************** No Phone Calls EEO/VET/LGBTQ+ Employer
    $58k-87k yearly est. 60d+ ago
  • Associate Scientist (JP9757)

    3 Key Consulting

    Chemist Job In West Greenwich, RI

    Employment Type: Contract Duration: 18 months with likely extensions Note: Onsite Essential 3 Key Consulting is hiring an Associate Scientist for a consulting engagement with our direct client, a leading global bio-pharmaceutical company. Job Summary: Bachelors' degree & 2+ years of Industry experience. To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. Experience in at least 1 of these analytical technologies: HPLC, ELISA, Capillary Electrophoresis, qPCR Responsibilities include: Lab based role Performing analytical testing in the lab to support a variety of studies following methods and procedures. Making mobile phases using standard lab equipment (pH meters, balances, pipettes). Troubleshooting equipment issues if needed. Communicating to the group and discussing data at meetings. Follows established experimental design and procedures and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision. Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data. Communicates data and interpretation to work group. Skilled at developing systems to ensure quality data. Skilled and/or knowledgeable in the use of standard laboratory equipment (pH meter, balances, pipettes) and with one or more major laboratory instruments/techniques (HPLC, ELISA, CE, qPCR). Effectively trouble-shoots equipment and experimental difficulties. Participates in department-wide support efforts such as safety. May train staff. Coordinates and organizes resources needed to complete the task. Understands when to seek input and when to make independent judgments. Degree in Biology, Biochemistry or Analytical Chemistry; experience in a Biopharmaceutical working environment. Top Must have Skill Sets: Industry experience 2+ years Great communication skills Experience with either HPLC, ELISA, CE or qPCR testing Day-To-Day Responsibilities: Employee Value Proposition: To work with a dynamic team and gain additional experience Red Flags: No industry experiences Large gap between jobs Interview Process: Phone screening, then webex video interview (2 total interviews) We invite qualified candidates to send your resume to **************************. If you decide that you're not interested in pursuing this position, please feel free to look at other positions on our website *********************** You are welcome to also share this posting with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team
    $68k-100k yearly est. Easy Apply 60d+ ago
  • Controller Associate

    International Paper 4.5company rating

    Chemist Job In Providence, RI

    **Physical Location:** **_Multiple Locations- Must be willing to relocate in the immediate future and eventually travel up to 50% as needed._** **Pay Rate** : $65,100 - $86,800 Multiple factors, including Individual experience, skills and abilities will determine where an employee is ultimately placed in the pay range. Variable pay may provide additional opportunities for financial awards. This job is eligible to participate in IP's annual incentive plan. **Category/Shift** : Salaried Full-Time **The Job You Will Perform:** - Work under the daily guidance of the site controller as part of a division-wide finance development program, gaining exposure to all aspects of the Container business through formal training, cross-site job rotations, special projects, and mentorship from NAC Finance leadership. - Generally, serve as one of two exempt financial professionals at the manufacturing site, typically working alongside a team that includes non-exempt staff-offering valuable leadership and managerial development opportunities as you progress. - While building the skills necessary for future leadership roles within the Finance organization, provide support to the plant controller, plant general manager, region controller, and NAC division staff. - Key responsibilities include ensuring strong internal controls to protect company assets, preparing financial statements in accordance with professional and corporate standards, delivering timely and actionable financial analysis, identifying and proposing solutions to business challenges, and mentoring and developing accounting staff. **The Skills You Will Bring:** - Bachelor's degree in Accounting, Finance, or Business Administration, with at least 12 credit hours in Accounting - Minimum of 2 years' experience in an Accounting or Finance role; experience in a converting facility is a plus - Geographic flexibility and willingness to travel up to 50% during the training period - Strong initiative and self-motivation, with excellent written, verbal, and active listening skills - Proven ability to collaborate effectively and contribute to team success - Comfortable working in a manufacturing environment - Strong knowledge of general and cost accounting, including month-end close processes and financial statement preparation - Experience with developing, maintaining, and assessing internal controls - Strong analytical and financial skills, including budgeting, forecasting, KPI tracking, working capital management, and supporting special projects - Familiarity with financial and operational information systems, preferably SAP, including system oversight and management - Understanding of sales, marketing, and distribution processes - Knowledge of quality improvement and manufacturing processes, including root cause analysis and implementation of corrective actions **The Benefits You Will Enjoy:** International Paper offers a benefits package that includes health, welfare and retirement plans including Medical, Dental, Life insurance, Flexible Spending Accounts, Short-term and Long-term Disability, 401(k), Company-funded retirement contributions, Paid Time Off, Education & Development (including Tuition Reimbursement), Student Loan Repayment Assistance, and Voluntary Benefits including insurance for home, auto, vision and pets. **The Impact You Will Make:** We continue to build a better future for people, the planet, and our company! IP has been a good steward of sustainable practices across communities around the world for more than 120 years. Join our team and you'll see why our team members say they're **Proud to be IP** . **The Culture You Will Experience:** International Paper promotes employee well-being by providing safe, caring and inclusive workplaces. We have team members all around the world with diverse backgrounds, experiences, and perspectives. These are our strengths. We are committed to creating a culture where all individuals are respected, valued, engaged and have an opportunity to do their best work every day. We invite you to bring your uniqueness, creativity, talents, experiences, and safety mindset to be a part of our increasingly inclusive and diverse culture. **The Company You Will Join:** International Paper (NYSE: IP) is the global leader in sustainable packaging solutions. With company headquarters in Memphis, Tennessee, USA, and EMEA (Europe, Middle East and Africa) headquarters in London, UK, we employ more than 65,000 team members and serve customers around the world with operations in more than 30 countries. Together with our customers, we make the world safer and more productive, one sustainable packaging solution at a time. Net sales for 2024 were $18.6 billion. In 2025, International Paper acquired DS Smith creating an industry leader focused on the attractive and growing North American and EMEA regions. Additional information can be found by visiting internationalpaper.com Share this job: Location: STATE WIDE, AL, US, #STATE WIDE, NC, US, #STATE WIDE, GA, US, #STATE WIDE, NE, US, #STATE WIDE, LA, US, #STATE WIDE, RI, US, #STATE WIDE, MI, US, #STATE WIDE, MN, US, #STATE WIDE, NJ, US, #STATE WIDE, SD, US, #STATE WIDE, IL, US, #STATE WIDE, TX, US, #STATE WIDE, OH, US, #STATE WIDE, NH, US, #STATE WIDE, OK, US, #STATE WIDE, TN, US, #STATE WIDE, ME, US, #STATE WIDE, MS, US, #STATE WIDE, WI, US, #STATE WIDE, CA, US, #STATE WIDE, WA, US, #STATE WIDE, KS, US, #STATE WIDE, MO, US, #STATE WIDE, NV, US, #STATE WIDE, SC, US, #STATE WIDE, IA, US, #STATE WIDE, CT, US, #STATE WIDE, IN, US, #STATE WIDE, OR, US, #STATE WIDE, VA, US, #STATEWIDE, VT, US, #STATE WIDE, NM, US, #STATE WIDE, NY, US, #STATE WIDE, MD, US, #STATE WIDE, MA, US, #STATE WIDE, UT, US, #STATE WIDE, AR, US, #STATE WIDE, CO, US, #STATE WIDE, FL, US, #STATE WIDE, PA, US, #STATE WIDE, AZ, US, #STATE WIDE, KY, US, # Category: Finance Date: Apr 2, 2025 If you are not finding suitable opportunities, please click below to join our talent community!
    $65.1k-86.8k yearly 60d+ ago
  • QC Analyst III - Microbiology

    Organogenesis, Inc. 4.8company rating

    Chemist Job In Smithfield, RI

    About Us We have unique opportunities and are always looking for exceptional talent. Join a company where you will have an opportunity to grow professionally and personally and give strength to others by Empowering Healing. Our advanced wound care products are specially developed for the successful treatment of chronic and acute wounds. Our comprehensive portfolio of skin substitutes and other regenerative medicine products empower our patients with life-changing solutions. Our surgical & sports medicine products support the healing of musculoskeletal injuries and degenerative conditions. Our strength is giving others strength. What You Will Achieve: The QC Analyst III performs complex quality activities in support of product production and releases. The position has interaction with other internal departments including, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also has interaction with external entities including contractors and suppliers. The QC Analyst III performs a wide variety of complex activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting results. Holiday work required on rotating basis. How You Will Achieve It: * Perform raw material, intermediate and non-routine testing * Perform endotoxin, microbiologic, and water testing * Perform reading environmental, personnel, and in-process sterility testing * Prepare and send out samples for microbiological identification and/or mycoplasma testing * Perform visual inspection of final product * Generate complex trend reports as they relate to quality testing * Revise SOPs * Responsible for interdepartmental interactions to ensure customer service needs are satisfied and priorities understood * Participate extensively in high-level quality systems programs (CAPA, etc.). * Provide input into failure investigations * Participates, contributes, and adds value in cross- functional settings. * Collaborates and communicates appropriately in all situations. * Looks for ways to reduce errors and costs. * Takes ownership for meeting all deliverables. * Responsible for initiating, investigating, and closing environmental monitoring excursion reports * Supporting preparation and adjustments to weekly schedule * Fast-paced high energy team-oriented work environment * Preparing and setting up the QC Micro laboratory to operational readiness Job Requirements What You Need to Achieve It: * Requires a Bachelor's Degree in Microbiology or related field * Minimum of 5-7 years of Microbiology experience in a GMP/Medical Device/ Pharmaceuical or Biological regulated environment * Experience in Aseptic Processing is preferred Physical Requirements: * This position may require a minimum of 25 hours/week gowned in classified areas; Class 100, 100K, 10K. * This position may require 2-3 hours of standing per day with frequent stooping and lifting What can we offer you? * 401k -- generous employer match with immediate vesting and financial planning resources * Comprehensive Medical, Dental and Vision coverage options effective on day one of employment * Flexible Spending Account (medical expenses or dependent care expenses) or Health Savings Account * Company paid insurances including Short Term, Long Term and Life insurances as well as voluntary options * Paid maternity leave and parental leave for all new parents * Adoption benefits * Education Assistance Policy - $5,000 per year for all employees * Wellness Program including free trainings on mental health, mindfulness, stress reduction, on-site flu shots and more * Employee Assistance Program * Generous paid time off including vacation, floating holidays, sick days, and company holidays * Free parking including an electric charging station (Canton and La Jolla) * Discounts at BJs Wholesale, Dell, Sullivan Tire, and Sprint The anticipated annualized base salary for a Level II role is $68,000-$81,000 and for a Level III is $81,000-$95,000 and reflects current market data for similarly-sized life science companies and internal equity. Organogenesis is a multi-state employer, and this salary range may not reflect positions that work in other states. Base salary is part of our total rewards package which also includes the opportunity for merit-based increases, eligibility for our 401(k) plan with competitive company match, medical, dental, vision, education assistance, life and disability insurances and leaves provided in line with your work state and federal law. Our time-off policy includes paid vacation days, paid company holidays, and paid sick time. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education, and other factors permitted by law. We are an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to age, sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, genetic information or any other characteristic protected by law. We do not accept unsolicited agency resumes and we are not responsible for any fees related to unsolicited resumes. Physical Required Job Type Full-time Location Organogenesis Rhode Island - Smithfield, RI US (Primary) Education Bachelor's Degree Career Level Individual Contributor Travel
    $81k-95k yearly 15d ago
  • Associate, Residential Servicing QC

    Situsamc

    Chemist Job In Providence, RI

    SitusAMC is where the best and most passionate people come to transform our client's businesses and their own careers. Whether you're a real estate veteran, a passionate technologist, or looking to get your start, join us as we work together to realize opportunities for everyone, we proudly serve. At SitusAMC, we are looking to match your unique experience with one of our amazing careers, so that we can help you realize your potential and career growth within the Real Estate Industry. If you are someone who can be yourself, advocate for others, stay nimble, dream big, own every outcome, and think global but act local - come join our team! This role will assist in running engagements or multiple engagements on a day-to-day basis. This role will assist in being the Subject Matter Expert and assist in reviewing residential loan scenarios and loan level questions needed by the Analyst and Senior Analyst before presenting such information to the manager. Included in this responsibility will be interfacing directly with Analysts and Senior Analysts on an as needed basis to assist in answering questions before escalating to the manager. This role should work with the manager to understand the timing of the engagement, ensure that required servicing data is available or, if such data is not available, that the manager is aware of the status to ensure that all necessary information has been acquired so the review to begin. If problems are identified, this role should notify the manager to remedy any issues. This role will assist in reviewing and implementing all investor and regulatory guidelines communicated and determine which communications impact the department and make any necessary revisions to scripts as needed. Essential Job Functions: + Review client responses/rebuttals and provide SitusAMC feedback as needed + Attend client calls as needed/required + Review all investor and regulatory communications and complete Compliance Committee change summary forms for management review + Add all relevant regulatory communications to the compliance tracker once change summary forms are approved + Implement any/all investor and regulatory changes by updating scripts as needed + Provide assistance and answer questions for analysts; escalate as needed + Host monthly meetings for Analysts and Senior Analysts to field any questions and discuss any regulatory updates and/or audit issues as a team + Assist with any special projects as needed, including any assigned reviews for specific clients + Assist in creating new exceptions in Clarity and periodically review exceptions to ensure they are updated with current information in a uniform manner and are active on appropriate scripts + As regulatory guidelines change, review and update the client document request lists to ensure prudent and up-to-date requests for loan audits are made + Assist and discuss any issues, questions, etc. + Other activities as may be assigned by your manager Qualifications/ Requirements: + College degree preferred or combination of education and experience + Experienced professional with 5+ years of industry and/or relevant experience, typically at a Senior Analyst or Analyst level role or external equivalent + Over five years in the mortgage industry preferred + Demonstrated ability to work with team members and clients + Strong excel skills + Team oriented + Ability to multitask + Excellent PC skills and possess high level of proficiency in Microsoft products + Strong communication (written and oral) skills + Strong analytical ability, good judgement, strategic and multidimensional thinker + Detail oriented and organized + Demonstrate professional behavior and teamwork, dependable and adhere to company policies and procedures. \#LI-Remote Note: This job description is not intended to be all inclusive or exclusive. At any time, employees may perform other related duties as required to meet the ongoing needs of the organization and participate in additional trainings. SitusAMC does not accept unsolicited resumes from staffing agencies, search firms or any third parties. Any unsolicited resume submitted to SitusAMC in any manner will be considered SitusAMC property, and SitusAMC will not pay a fee for any placement resulting from the receipt of an unsolicited resume. The annual full time base salary range for this role is $56,000.00 - $85,000.00 Specific compensation is determined through interviews and a review of relevant education, experience, training, skills, geographic location and alignment with market data. Additionally, certain positions may be eligible to receive a discretionary bonus as determined by bonus program guidelines, position eligibility and SitusAMC Senior Management approval. SitusAMC offers PTO and paid holidays, the terms of which are set forth in the program policies. All full time employees also are eligible to participate in various benefit plans, including medical, dental, vision, life, disability insurance and 401K; in each case in accordance with the terms of the applicable plans. Pay Transparency Nondiscrimination Provision (****************************************************************************************************** SitusAMC is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Know Your Rights, Workplace Discrimination is Illegal (*********************************************************************************************** SitusAMC does not accept unsolicited resumes from staffing agencies, search firms or any third parties. Any unsolicited resume submitted to SitusAMC in any manner will be considered SitusAMC property, and SitusAMC will not pay a fee for any placement resulting from the receipt of an unsolicited resume.
    $56k-85k yearly 53d ago
  • Office - Quality Control

    Evolution Wireless Inc.

    Chemist Job In East Providence, RI

    JOIN THE TEAM! Under the supervision of our Operations Director, you will be trained to ensure all company standards are met and maintained at each individual location. We are looking for responsible individuals that: Will be reviewing daily store status reports Documenting and tracking store readiness per the given guidelines. Observing locations using video monitoring systems to ensure and report the given sales process are being followed. The individual must stay up-to date on all current sales promotions and processes. Requirements: High school diploma or general education degree (GED), required Ability to use video monitoring equipment Ability to interpret a variety of instructions furnished in written, oral or schedule form Ability to work on the internet, Spreadsheet, Presentation and Word Processing software Strong written and verbal communication skills Must have the ability to complete required applicable forms in English, which requires the ability to read and write in English. Ability to work well with others in fast paced, dynamic environment. Ability to be respectful, approachable and team oriented while building strong working relationships and a positive work environment. .
    $26k-40k yearly est. 60d+ ago
  • Associate Quality Control

    Advanced Bio-Logic Solutions Corp 3.9company rating

    Chemist Job In West Greenwich, RI

    Note: 100% onsite RI Shift is Sat, Sun, Mon, Tue 6:45 AM- 5:15 PM 11 months duration with possible extension. Recent bachelors but with more lab experience than just academic experience Degree in Scientific field. Looking for an entry level lab position. Must have experience working within a team in a lab setting. Job Details: Under general supervision, this position will perform routine procedures to support testing within Quality Control. Tasks may include but not limited to performing sample collection, sample handling, testing equipment/laboratory support. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures Documenting, computing, compiling, interpreting, and entering data into computerized systems Maintaining and operating specialized equipment Initiating and /or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory notebooks. Skills: Some lab experience is preferred. no academic research experience, would like a GMP lap exp. Day to Day Responsibilities: Environmental Monitoring Water Collection Sample Management Read and Approvals of Samples Basic Qualifications High school/GED + 2 years work experience or Associates degree and 6 months work experience or Bachelors degree Must Have Skill Sets: GMP/GDP/GLP experience Laboratory Skills Can work in teams and independently Scrubbed resume attached Ideal candidate: Understands the importance of GMP and the why behind a regulated industry. Recent bachelors but with more lab experience than just academic experience Degree in Scientific field. Looking for an entry level lab position. Must have experience working within a team in a lab setting. Pay Rate between $29 - $33/Hr. on W2 based on experience. "This posting is for Contingent Worker, not an FTE"
    $29-33 hourly 28d ago
  • Quality Control Senior Associate

    Volt 4.4company rating

    Chemist Job In West Greenwich, RI

    Innova Solutions has a client that is immediately hiring a Quality Control Senior Associate. Position type: Full-time - Contract Duration: 12 Months As a Quality Control Senior Associate, you will: Description Ideal Candidate: 1-2 years of experience in a GMP setting + a B.S. Please review the top 3 skillsets. Job Details: Under general supervision, this position will perform routine procedures to support drug substance and drug product testing within Quality Control. Tasks may include but are not limited to performing sample collection, sample handling, testing equipment/laboratory support. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Documenting, computing, compiling, interpreting, and entering data into computerized systems - Maintaining and operating specialized equipment - Initiating and /or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory notebooks. What we are looking for: Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy. Must have focus on data integrity Experience: Master's degree OR Bachelor's degree and 1-2 years of Quality or Analytical Laboratory experience OR Associate's degree and 3-5 years of Quality or Analytical Laboratory experience OR High school diploma/GED and 5 years of Quality or Analytical Laboratory experience Preferred Qualifications Experience in GMP analytical laboratory Experience with HPLC/UPLC, general chemistry, capillary electrophoresis Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories. Understanding of biopharmaceuticals process and related unit operations Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy Independent, self-motivated, organized, able to multi-task in time-sensitive environments. Demonstrated experience in investigations and QC processes Qualified candidates should APPLY NOW for immediate consideration! Please hit APPLY to provide the required information, and we will be back in touch as soon as possible. We are currently interviewing to fill this and other similar positions. If this role is not a fit for you, we do offer a referral bonus program for referrals that we successfully place with our clients, subject to program guidelines. ASK ME HOW. Thank you! Pradip Joshi Email - ...@innovasolutions.com Phone: 213-###-#### PAY RANGE AND BENEFITS: Pay Range*: $20- $23/Hr *Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc. Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). ABOUT INNOVA SOLUTIONS: Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields. Recent Recognitions: Named One of America's Best Employers for New Grads by Forbes (2024 Named One of the Best Companies to Work For by U.S. News & World Report (Private Companies List, 2024-2025) One of the Largest IT Staffing Firms in the US - Ranked #3 by Staffing Industry Analysts (SIA, 2024) One of the Largest Staffing Firms in the US - Ranked #13 by Staffing Industry Analysts (SIA, 2024; includes Innova Solutions, Volt, & HireGenics) Named One of the Top Ten Private Companies in Atlanta by the Atlanta Business Chronicle (2023) One of the Largest Certified Minority Business Enterprises (MBEs) in the United States (NMSDC, 2024) AWS Advanced Tier Services Partner with 100+ certifications Website: /> Innova Solutions is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please contact us at ...@innovasolutions.com or (770) ###-####. Please indicate the specifics of the assistance needed. Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities. Innova Solutions (HireGenics/Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws. Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). ABOUT INNOVA SOLUTIONS: Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields. Recent Recognitions: One of Largest IT Consulting Staffing firms in the USA - Recognized as #4 by Staffing Industry Analysts (SIA 2022) ClearlyRated Client Diamond Award Winner (2020) One of the Largest Certified MBE Companies in the NMSDC Network (2022) Advanced Tier Services partner with AWS and Gold with MS Innova Solutions is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please call (770) ###-####. Please indicate the specifics of the assistance needed. Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities. Innova Solutions (HireGenics/Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.
    $20-23 hourly 1d ago
  • R&D Chemist

    Fujifilm 4.5company rating

    Chemist Job In North Kingstown, RI

    **FUJIFILM Electronic Materials, U.S.A., Inc.,** is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our North Kingstown, RI facility for an **R&D Chemist!** With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process. **The Role** The successful candidate will lead the development and optimization of new platforms for photoimageable dielectric materials. This role involves collaboration with central R&D and product technology teams to drive raw material selection and formulation improvements. The ideal candidate will have a strong background in polymer synthesis and organic chemistry, with expertise in design, synthesis, and characterization of new materials. Additionally, the R&D Chemist will apply experimental design, problem-solving skills, and root cause analysis to innovate and enhance product performance, while providing support in troubleshooting material-related issues. **Company Overview** FUJIFILM Electronic Materials, U.S.A., Inc. is a wholly owned subsidiary of FUJIFILM Holdings America Corporation. FUJIFILM Electronic Materials, U.S.A., Inc. supplies the world's top semiconductor manufacturers with a broad array of products and services, including chemicals and advanced materials. The company's broad product portfolio includes high-purity acids/bases, photoresists, thin film formation materials, formulated products, CMP slurries, and polyimides for advanced packaging. The company has six state-of-the-art manufacturing facilities and research labs in the U.S., including Arizona, California, Colorado, Rhode Island, and Texas. For more information, please visit: ************************************* . FUJIFILM Corporation is a subsidiary of FUJIFILM Holdings Corporation. FUJIFILM Holdings Corporation, headquartered in Tokyo, leverages its depth of knowledge and proprietary core technologies to deliver innovative products and services across the globe through the four key business segments of healthcare, electronics, business innovation, and imaging with over 70,000 employees. Guided and united by our Group Purpose of "giving our world more smiles," we address social challenges and create a positive impact on society through our products, services, and business operations. Under its medium-term management plan, VISION2030, which ends in FY2030, we aspire to continue our evolution into a company that creates value and smiles for various stakeholders as a collection of global leading businesses and achieve a global revenue of 4 trillion yen (29 billion USD at an exchange rate of 140 JPY/USD). For more information, please visit: ************************ . For further details about our commitment to sustainability and Fujifilm's Sustainable Value Plan 2030,click here (************************************************************* . **Job Description** **Key responsibilities for this role include:** + Lead the design and development of new platforms for photoimageable dielectric materials, contributing to innovative advancements in the industry. + Drive the selection of new raw materials by collaborating closely with the central division R&D and product technology teams, supporting the design, synthesis, and characterization of novel materials. + Optimize product formulations by integrating new raw materials, performance criteria, and customer requirements to achieve superior product outcomes. + Utilize in-depth knowledge of polymer synthesis and organic chemistry to develop new polymer platforms and raw materials, including designing structures, developing synthetic routes, and characterizing the developed materials. + Apply expertise in the design of experiments, problem-solving methods, and root cause analysis to innovate and improve processes and products. + Provide support in troubleshooting material-related issues, ensuring efficient resolution and continuous improvement. **REQUIREMENTS** + Bachelor's degree in Chemistry, Chemical Engineering, Materials Science, or a related field. Master's or PhD in Chemistry strongly preferred. + 3-5 years of experience in organic chemistry, polymer synthesis, or related fields + Experience in semiconductor lithography or related fields strongly preferred. + Strong background in the design, development, and characterization of new materials. + Hands-on experience with product formulation and raw material selection. + Extensive knowledge of polymer synthesis and organic chemistry principles. + Proficiency in designing synthetic routes and characterizing developed materials. + Expertise in the design of experiments (DOE) and statistical analysis. + Proven ability to apply problem-solving methods and conduct root cause analysis. + Familiarity with material characterization techniques and instrumentation. + Must have excellent capability to use PowerPoint, Excel, or other software tools to generate first-class presentations. + Strong analytical and critical thinking skills. + Excellent communication and collaboration abilities. + Ability to work effectively in cross-functional teams. + High level of self-motivation and initiative. + Strong project management and organizational skills. **MENTAL & EMOTIONAL REQUIREMENTS** + **Resilience -** Adapting well in the face of workplace stressors, the ability to work effectively and efficiently in high stress and conflict situations, the ability to remain poised under all circumstances, the ability to maintain regular attendance and be punctual. + **Communication -** The ability to successfully and professionally express and exchange ideas and meanings with all levels of employees in the organization, the ability to interact appropriately with a variety of individuals including customers/clients, the ability to work as an integral part of a team, ability to interact effectively with people in a positive manner that engenders confidence and trust. + **Reasoning and decision-making -** The ability to understand, remember and follow verbal and written instructions, the ability to reason logically and make sound decisions. + **Comprehension -** The ability to complete tasks without direct supervision, the ability to simultaneously address multiple complete problems. + **Organizational skills -** Ability to multitask without loss of efficiency or accuracy, the ability to work and sustain attention with distractions and interruptions, the ability to perform in situations requiring speed, deadlines or productivity quotas. **To all agencies: Please, no phone calls or emails to any employee of Fujifilm about this requisition. All resumes submitted by search firms/employment agencies to any employee at Fujifilm via-email, the internet or in any form and/or method will be deemed the sole property of Fujifilm, unless such search firms/employment agencies were engaged by Fujifilm for this requisition and a valid agreement with Fujifilm is in place. In the event a candidate who was submitted outside of the Fujifilm agency engagement process is hired, no fee or payment of any kind will be paid.** **EEO Information** Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. **ADA Information** If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (********************************). **Job Locations** _US-RI-North Kingstown_ **Posted Date** _2 weeks ago_ _(3/20/2025 5:00 PM)_ **_Requisition ID_** _2025-33552_ **_Category_** _R & D_ **_Company (Portal Searching)_** _FUJIFILM Electronic Materials U.S.A_
    $105k-136k yearly est. 40d ago
  • Chemist

    Actalent

    Chemist Job In Providence, RI

    We are seeking a dedicated Chemist to join our dynamic team. This role involves following permit requirements to collect and test compounds and samples using applied methods and techniques while adhering to company policies. You will be responsible for entering quantities, volumes, and analytical results into our waste management software (WMS/Preview), assisting with QA/QC analytical screening parameters as dictated by permits, and following all approved Laboratory SOPs. Ensuring compliance with environmental health and safety standards, including the proper handling, storage, and disposal of chemical agents, is essential. Additionally, you will assist in operating and maintaining laboratory equipment. Responsibilities + Collect and test compounds and samples per permit requirements. + Enter quantities, volumes, and analytical results into waste management software (WMS/Preview). + Assist with QA/QC analytical screening parameters. + Follow all approved Laboratory SOPs. + Ensure compliance with environmental health and safety standards, including proper handling, storage, and disposal of chemical agents. + Assist in operating and maintaining laboratory equipment. Essential Skills + Bachelor's degree in sciences (no experience required) + Associate degree in science with some laboratory experience + High School Diploma with at least one year of industry or academic laboratory experience + Proficiency in Excel and Word + Strong communication and written skills + Ability to stand for long periods + Capability to work in a fast-paced environment handling 100+ samples daily Additional Skills & Qualifications + Experience with pipetting, distillation, data analysis, pH testing, quality control, chemical handling, and wastewater treatment + Knowledge of Laboratory SOPs + Familiarity with WMS/Preview waste management system Work Environment You will be working with a growing team of 10 technicians within a fast-paced laboratory environment. The work schedule is Monday to Friday, 9 am to 5 pm, and the dress code is business casual with close-toed shoes. Personal protective equipment (PPE) will be provided on-site. The company culture emphasizes growth and internal advancement, with numerous opportunities to develop your career within the organization. There is a robust training program designed to help you gain valuable industry laboratory experience and exposure to SOPs and chemical testing. If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com. Pay and Benefits The pay range for this position is $22.00 - $22.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision- Critical Illness, Accident, and Hospital- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available- Life Insurance (Voluntary Life & AD&D for the employee and dependents)- Short and long-term disability- Health Spending Account (HSA)- Transportation benefits- Employee Assistance Program- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Providence,RI. Application Deadline This position is anticipated to close on Apr 4, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
    $22-22 hourly 10d ago
  • Associate Scientist - (JP10311)

    3 Key Consulting

    Chemist Job In West Greenwich, RI

    Employment Type: Contract Business Unit: Commercial Attribute Sciences Duration: 18+ months (with likely extensions) Notes: Only qualified candidates, please. Bachelors' degree & 2 YOE. Must be onsite. Posting Date: 05/25/22 3 Key Consulting is hiring an Associate Scientist for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. Responsibilities include: Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision. Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data. Effectively transfers experimental methods from literature to the lab and makes modifications as necessary. Develops and implements new protocols with moderate review. Engages coworkers in scientific discussions. Communicates data and interpretation to work group. Skilled at developing systems to ensure quality data. Skilled and/or knowledgeable in the use of standard laboratory equipment and with one or more major laboratory instruments/techniques. Effectively trouble-shoots equipment and experimental difficulties. Contributes to internal/external reports, papers, presentations, regulatory documents. Participates in department-wide support efforts such as safety. May train others. Coordinates and organizes resources needed to complete the task. Understands when to seek input and when to make independent judgments. Basic Qualifications: Degree in Biology, Biochemistry or Analytical Chemistry ; experience in a Biopharmaceutical working environment Why is the Position Open? Supplement additional workload on team. Top Must-Have Skill Sets: 2+ years of HPLC experience Hands on analytical testing experience Organized; great attention to detail Experience working in a lab setting Day to Day Responsibilities: Analytical testing Equipment troubleshooting Solution prep Documentation in Electronic Lab Notebook Safety and chemical lab sweeps Employee Value Proposition: Unique lab experience, growth opportunity Red Flags: Gap in employment history Too many short term jobs Interview process: Phone screening followed by in-person interview. We invite qualified candidates to send your resume to **************************. If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website ******************************* You are also welcome to share this opportunity with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team
    $68k-100k yearly est. Easy Apply 60d+ ago
  • QC Analyst II/III Materials

    Organogenesis, Inc. 4.8company rating

    Chemist Job In Smithfield, RI

    What You Will Achieve: The QC Analyst II/III performs quality activities in support of quality disposition of materials: material inspection, material testing coordination, data collation, data review, material shipments, document updates etc.. The position interacts with other internal departments, including Production Departments (Apligraf FortaFlex, Dermagraft, Trancyte, Human Tissue Manufacturing, Cell Culture, Cell Banking etc.), Quality Assurance, Materials Management, and Logistics. The position also has interactions with external entities including contractors, test labs and suppliers. The QC Analyst II/III performs a wide variety of activities to ensure compliance with applicable regulatory requirements in support of inspecting, coordinating testing, trending, and reporting results. The QC Analyst II/III will support QC Material compliance including but not limited to: Change Notifications, non-conforming raw materials, internal/external deviations, OOTr/OOS results etc. The QC Analyst II/III will support continuous improvement initiatives and participate in Quality System requirements for new and existing materials, e.g. risk management, CAPA and change controls. Periodic weekend, holiday and evening on-call coverage may be required. This position directly supports all activities with QC Materials in direct support of Class II and Class III medical devices that will be manufactured in a new CGMP facility located in Rhode Island. This position will initially be based out of the Canton, MA facility requiring 20% - 50% travel between the Massachusetts Campus and the new facility in Smithfield, RI. Eventual home office at the RI facility with continued 20-30% travel to support Canton material activities as needed. How You Will Achieve It: * Perform material inspections. * Perform tissue inspections. * Submit test requests to the QC functional areas to coordinate testing. * Coordinate shipping of materials to external test labs. * Collate results and document results to submit to Quality Assurance for final dispositioning. * Author and Revise SOPs. * Generate trend reports as they relate to Quality Control testing, release metrics. * Responsible for interdepartmental interactions to ensure customer service needs are satisfied and priorities understood. * Perform material related Quality System activities: Deviations; Non-conforming material reports; Internal Audit responses, risk assessments, change controls etc. * Support material qualifications in compliance with company policies and applicable regulatory guidelines. * Support continuous improvement projects Job Requirements What You Need to Achieve It: * Bachelor's degree in science or equivalent * 4-7 years of related experience in a GMP regulated QC environment in support of FDA regulated Medical Devices and Biologics * Materials and/or final product inspection experience required * Pharmacopeia experience required * Local travel between OI production sites will be required (Canton MA, Norwood MA, Smithfield RI) * On-site position Physical Requirements: * Pass Annual Vision Screening Test * Able to lift 50 lbs. and 25-50% of time standing in workday What can we offer you? * 401k -- generous employer match with immediate vesting and financial planning resources * Comprehensive Medical, Dental and Vision coverage options effective on day one of employment * Flexible Spending Account (medical expenses or dependent care expenses) or Health Savings Account * Company paid insurances including Short Term, Long Term and Life insurances as well as voluntary options * Paid maternity leave and parental leave for all new parents * Adoption benefits * Education Assistance Policy - $5,000 per year for all employees * Wellness Program including free trainings on mental health, mindfulness, stress reduction, on-site flu shots and more * Employee Assistance Program * Generous paid time off including vacation, floating holidays, sick days, and company holidays * Free parking including an electric charging station (Canton and La Jolla) * Discounts at BJs Wholesale, Dell, Sullivan Tire, and Sprint The anticipated annualized base salary for a Level II role is $68,000-$81,000 and for a Level III is $81,000-$95,000 and reflects current market data for similarly-sized life science companies and internal equity. Organogenesis is a multi-state employer, and this salary range may not reflect positions that work in other states. Base salary is part of our total rewards package which also includes the opportunity for merit-based increases, eligibility for our 401(k) plan with competitive company match, medical, dental, vision, education assistance, life and disability insurances and leaves provided in line with your work state and federal law. Our time-off policy includes paid vacation days, paid company holidays, and paid sick time. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education, and other factors permitted by law. We are an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to age, sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, genetic information or any other characteristic protected by law. We do not accept unsolicited agency resumes and we are not responsible for any fees related to unsolicited resumes. Physical Required Job Type Full-time Location Organogenesis Inc. Headquarters Shipping Address/Apligraf Manufacturing - Canton, MA 02021 US (Primary) Organogenesis Rhode Island - Smithfield, RI US Education Bachelor's Degree Career Level Individual Contributor Travel 40 - 50%
    $81k-95k yearly 17d ago

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