Chemist Jobs in Hamden, CT

Come join P2 Science, a Connecticut Innovations portfolio company! https:/p2science.com Founded in 2009, P2 Science was started by two scientists from Yale University, who were disheartened by the widespread use of non-sustainable, synthetic compounds found in everyday use. P2 Science started with a simple vision - develop high performance, innovative ingredients that align with planetary health. P2 Science has become a global leader in bringing naturally derived, sustainable ingredients to market; partnering with brands and manufacturers in 25 countries. Through a proprietary process called Process Intensified Continuous Etherification ("PICE"), P2 transforms renewable forest-derived feedstocks into high-performance ingredients for use in a variety of personal care, cosmetics, and beauty products. The company started up its first manufacturing plant in September 2018. In 2022, P2 won five industry awards, including the Innovation Best Breakthrough Supplier Award from BeautyMatter, one of the most trusted voices in beauty. In January 2023, Unilever's haircare brand, Living Proof, launched three new products built on P2's ingredients. In November 2023, P2 Science announced the appointment of Oihana Elizalde, PhD as Chief Executive Officer. Oihana joined P2 after having served as Head of Sales for BASF Personal Care North America, and VP / General Manager of the MIRUM business at Natural Fiber Welding. P2's investors include Advantage Capital, BASF, Chanel, Connecticut Innovations, Elm Street Ventures, HG Ventures, Lewis & Clark Agrifood, Safermade, and Xeraya. Quality Control Chemist Position Summary: Troubleshooting and testing batches using a variety of QC instruments, while ensuring strict adherence to regulatory standards and maintaining quality in a high-pressure environment. Responsibilities / Job Functions Responsible for overseeing manufacturing QC activities. Prepare, run, and analyze final product and in-process samples, ensuring QC testing is conducted using appropriate, established company methods (work instructions, standard operating procedures). Maintain accurate, complete, and traceable documentation related to analysis. Assist in completing and submitting lab documentation, including deviation investigations, OOS (Out of Specification) investigations, change controls, and their implementation. Perform calibration, troubleshooting, and maintenance of lab instrumentation; assist with scheduling annual Preventive Maintenance (PM). Prepare relevant documents, forms, and records related to QC in compliance with ISO 9001:2015 guidelines. Ensure successful, on-time completion of required training (both internal and external). Adhere to safety standards and regulations as per ISO 9001:2015, Food Safety 22000 requirements, and other company-established policies. Safety Responsibility Comply with all P2 safety policies and procedures. Qualifications B.S. in Chemistry or related field is required. 2-3 years of experience in: QC or raw material testing OOS (Out of Specification) or deviation reporting Experience in a GLP (Good Laboratory Practice) or GMP (Good Manufacturing Practice) environment is a plus Analytical instrumentation, such as GC, HPLC, DSC, viscometer, refractometer, NMR, UV-Vis, KF titration, and other titration methods. Strong attention to detail with excellent oral and written communication skills. Ability to multitask and collaborate effectively across departments. Flexibility to work overtime as needed or adjust schedule to meet manufacturing needs. Ability to lift up to 50 lbs. Why Join Us? Be part of a dynamic team that's leading the way in sustainable beauty innovation. Work in an environment that values creativity, sustainability, and inclusivity. Competitive salary and benefits package, including health, dental, and vision insurance, paid time off, and retirement savings plans. Opportunities for professional growth and development within the company. Make a positive impact on the planet and society through your work. P2 is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Under supervision, an employee in this class performs entry level professional work conducting quantitative analyses on samples from marine and fresh surface waters, groundwater and industrial and domestic wastewater sources. An important aspect of this position is that its primary purpose is to monitor the composition of ground and surface waters so as to detect and guard against pollution. The work involves the supervised use and general maintenance of sophisticated modern laboratory equipment such as an auto-analyzer, an atomic absorption spectrophotometer, an organic carbon analyzer and a gas chromatograph. The incumbent performs some preparatory and routine functions independently, but performs more complex assignments under either direct or general supervision, depending upon the level of difficulty. Direct supervision may be exercised over the work of Laboratory Technicians and Aides. * Does related work as required. KEY RESPONSIBILITIES: * Sets up, calibrates and runs automated analysis equipment to quantitatively analyze water, industrial and domestic wastewater, and septage samples; * Performs and directs Laboratory Technicians and Aides in the performance of wet method sample preparations, simple colorimetric tests and other simple volumetric, spectrophotometric and gravimetric analyses; * Performs analyses associated with the control and determination of performance of wastewater treatment facilities; * Prepares materials for use by washing, measuring, cooking, etc.; * Makes up reagents for use in chemical tests; * Receives and logs in samples, divides into smaller samples, labels and stores properly; * Reads charts of test results, calculates numerical equivalents and transfers to log sheets; * Checks to make sure that sufficient quantities of supplies are on hand; * May be required to testify in court as to findings and observations; * May wash glassware and perform other clean-up activities. Benefits For You Now And Your Future * Health Insurance: Suffolk offers a comprehensive health insurance plan, including medical, dental, and vision coverage * Pension * Paid Time Off: Vacation (2 weeks to start) is accrued based on length of service; sick leave allows employees to take time off for illness without sacrificing pay; personal days can be used for a variety of reasons; and thirteen (13) paid holidays. * Work-Life Balance: County jobs offer regular working hours, reducing the need for overtime or irregular shifts. This helps employees maintain a good work-life balance. Overall, county government jobs offer a combination of competitive benefits and job security, making them an attractive option for many job seekers. * This position does not offer relocation assistance at this time Sponsorship is not available for this role Starting Salary: $54,392 to $88,531 OPEN COMPETITIVE Graduation from a college with federally-authorized accreditation or registration by NY State with a Bachelor's degree in one of the natural sciences which includes at least sixteen (16) credit hours in Chemistry including Organic Chemistry. PROMOTIONAL Two (2) years of permanent competitive status as a Laboratory Technician or a Laboratory Technician (Public Works) possessing a Bachelor's degree in one of the natural sciences with at least sixteen (16) credit hours in Chemistry including Organic Chemistry. ADDITIONAL POSITION DETAILS: * Good knowledge of the theories, principles and practices of organic and analytical chemistry * Good knowledge of mathematics * Good knowledge of modern chemical laboratory methods, procedures and equipment * Good knowledge of the indicators, sources and legal limits of water pollutants * Working knowledge of statistics * Skill in laboratory manipulative techniques * Ability to take field samples and to set up sampling procedures * Ability to operate complex electronic laboratory equipment * Ability to perform assigned analyses and tests according to prescribed procedures * Ability to make accurate observations and conclusions of test results * Ability to maintain good working relationships with others in close quarters * Patience * Persistence * Physical condition commensurate with the demands of the position. Suffolk County's Commitment to Diversity, Inclusion & Equity: * Our focus is to promote, support, and implement the County-wide diversity and inclusion strategic plan. * We achieve results in all our responsibilities through the use of diversity and inclusion best practices. * We maintain a familiarity with Diversity & Inclusion trends and best practices. Suffolk County is an Equal Employment Opportunity Employer and does not discriminate against applicants or employees on the basis of race, color, religion, creed, national origin, ancestry, disability that can be reasonably accommodated without undue hardship, sex, sexual orientation, gender identity, age, citizenship, marital or veteran status, or any other legally protected status.

At Henkel, you can build on a strong legacy and leading positions in both industrial and consumer businesses to reimagine and improve life every day. If you love challenging the status quo, join our community of over 47.000 pioneers around the globe. Our teams at Henkel Adhesive Technologies help to transform entire industries and provide our customers with a competitive advantage through adhesives, sealants and functional coatings. With our trusted brands, our cutting-edge technologies and our disruptive solutions, you will have countless opportunities to explore new paths and develop your skills. Grow within our future-led businesses, our diverse and vibrant culture and find a place where you simply belong. All to leave your mark for more sustainable growth. Dare to make an impact? What you´ll do * Design, develop, execute, and support on-time commercialization of new adhesive formulations and products. * Prepare and deliver presentations on research projects for internal teams, management, customers, and technical conferences. * Understand state-of-art technology advancement and apply it to product development. Generate new intellectual properties. * Perform all laboratory work in a safe manner and comply with all regulations, safety precautions, PPE requirements, and 5Sprocesses. * Guide and mentor junior chemists as needed. What makes you a good fit * Master's or PhD degree in Chemistry, Chemical Engineering, Polymer Sciences, Materials Science, or in any other related scientific areas, is highly preferred. * Candidate with B.S. degree and a strong track record of >10 years of successful Product Development in the relevant area may be considered. * Proven track record of on-time product development delivery from idea generation to completion is required. * Minimum 5 years of experience in the areas of UV/Light stable Epoxy (1K & 2K) resin for outdoor applications. * Strong oral and written communication skills, and excellent interpersonal skills are essential. * The ability to work autonomously on multiple projects is needed. * Traveling of up to 10% will be required. Some perks of joining Henkel * Flexible or hybrid work model * Diverse national and international growth opportunities * Global wellbeing standards with health and preventive care programs * Gender-neutral parental leave for a minimum of 12 weeks * Employee Share Plan with voluntary investment and Henkel matching shares * Annual performance bonus * Comprehensive healthcare including mental health support and 401(k) plan matched by employer * Family benefits including fertility support, fully paid parental leave, caregiver services * Paid time off: Vacations days, sick leave, holidays, volunteer time off & more The salary for this role is $120,000.00- $145,000.00. This is the range that we in good faith anticipate relying on when setting wages for this position. We may ultimately pay more or less than the posted range and this range. This salary range may also be modified in the future. Henkel does not accept unsolicited resumes from search firms or employment agencies. Unsolicited referrals and resumes are considered Henkel property and therefore, Henkel will not pay a fee for any placement resulting from the receipt of an unsolicited referral. Henkel is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information, and other legally protected categories. JOB ID: 25074749 Job Locations: United States, CT, Rocky Hill, CT Contact information for application-related questions: ***************************** Please do not use this email address for sending your application or CV. To apply, please click on the "Apply for this role" button below. Applications sent via e-mail will not be accepted. Application Deadline: As long as the vacancy is listed on our Career Site, we are happy to receive your application Job-Center: If you have an application already, you can create or log in to your account here to check the status of your application. In case of new account creation, please use your email address that you applied with. Activate external content When clicking the button below external content will be loaded which involves transfer of personal data (e.g. IP address) to external servers. This may involve that cookies are set by the external content provider. Please see Data Protection Statement for further information. Accept for all YouTube content LOAD EXTERNAL CONTENT Deactivate loading external content from YouTube. How is work at Henkel About Henkel Building on a strong legacy of almost 150 years, we are leading the way to reimagine and improve life every day. Today and for generations to come. Through our innovative and sustainable brands and technologies, across our teams around the world. Henkel holds leading positions in both industrial and consumer businesses: Our portfolio includes well-known hair care products, laundry detergents, fabric softeners as well as adhesives, sealants, and functional coatings.

Analytical Chemist specializing in Distillation Are you enthusiastic about advancing your expertise in chemistry, particularly in the field of analytical methods? Join our innovative team as an Analytical Chemist with a focus on distillation, where your analytical skills will be essential for the purification of organic compounds utilizing sophisticated distillation techniques. Position Overview: In this role, you will conduct advanced processing operations aimed at the purification of organic materials through cutting-edge distillation systems. You will be responsible for handling various chemical substances, performing in-depth analyses of their compositions, and maintaining meticulous batch process documentation-all while contributing to our commitment to environmental sustainability. Key Responsibilities: * Set up and optimize distillation apparatus, ensuring the effective operation of heating, cooling, vacuum, and pressure systems. * Precisely transport, weigh, mix, and pump a variety of chemical substances, adhering to strict protocols. * Employ analytical instrumentation to assess the quality of distillation fractions and final products; analyze and interpret data to confirm compliance with established standards, and modify processes in the event of deviations. * Monitor vital process parameters to ensure optimal product quality, yield, and consistency across batches; identify opportunities for enhancement and recommend corrective actions. * Assist in the preparation of comprehensive test results and technical reports as required. * Uphold highest safety and maintenance standards for all technology, equipment, and laboratory environments. * Maintain an organized and sanitary workspace to ensure both safety and operational efficiency. * Provide mentorship and support to Distillation Technicians and junior Analytical Chemists, serving as a resource for training and knowledge sharing. Qualifications: * A Bachelor's degree in Chemistry, Analytical Chemistry, Environmental Science, or a related discipline from an accredited institution is preferred. * 2 to 5 years of practical experience in distillation and analytical chemistry techniques. * A solid understanding of vacuum distillation principles and proficiency in gas chromatography analysis. * An Associate's degree may be acceptable if coupled with significant hands-on experience and specialized training. Work Environment: * The role may involve exposure to hazardous materials and vapors, necessitating strict adherence to safety protocols and industry-standard training. Physical Requirements: * Capable of handling containers using mechanical assistance; tasks may include moving heavy 55-gallon drums (up to 700 lbs.) and lifting 5-gallon containers (up to 44 lbs.). * Must be comfortable with climbing stairs and using ladders and capable of standing or walking for extended periods (more than four hours daily). Safety Training Required: * OSHA HAZCOM training * Personal Protective Equipment (PPE) training * HAZWOPER training * Fall Protection training * Respirator Protection training Join Us: If you're prepared to elevate your career in a fast-paced and safety-focused environment committed to innovation, we invite you to apply for the position of our next Analytical Chemist specializing in Distillation! * Keep a cle Safety Training Required: * OSHA HAZCOM training * PPE (Personal Protective Equipment) * HAZWOPER * Fall Protection * Respirator Protection Join Us: If you're ready to advance your career in a dynamic environment dedicated to innovation and safety, apply to be our next Distillation Chemist today! Pay and Benefits The pay range for this position is $59000.00 - $78000.00/yr. Medical/Dental/Vision 401k Annual Bonus Generous PTO & paid holidays (shut down week of Christmas paid) Workplace Type This is a fully onsite position in Danbury,CT. Application Deadline This position is anticipated to close on May 7, 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.

Chemist (Manufacturing) – Direct Hire - $70K - $100K (DOE) Shape the Science Behind Innovative Manufacturing! Step into a role where chemistry meets innovation. Join a cutting-edge manufacturing team known for precision design, advanced processes, and a commitment to excellence. We’re partnering with a trusted industry leader to hire a Chemist for a direct hire opportunity. If you’re passionate about chemical processes, enjoy hands-on lab work, and want to make a real impact, this could be the perfect match. What You’ll Do: Ensure the integrity and consistency of product formulations, raw materials, and bonding procedures. Conduct in-depth chemical analyses using techniques like chromatography, spectroscopy, and titration. Serve as the Safety Officer, helping develop and enforce safety protocols for handling hazardous materials. Collaborate with cross-functional teams to drive product quality and workplace safety. What You’ll Bring: Education & Experience Bachelor’s degree in Chemistry, Chemical Engineering, or a related field. 3 – 5 years of experience in a manufacturing or industrial lab setting. Skills & Knowledge Strong understanding of chemical processes, materials, and lab equipment. Familiarity with OSHA, EPA, and other regulatory compliance standards, Proficiency with data analysis software and Microsoft Office Suite. Personal Attributes Detail-oriented with a critical-thinking mindset Strong communication skills and ability to work both independently and in a team. Comfortable in a hands-on manufacturing environment (including standing for a long periods and handling chemicals safely). Why Apply? Competitive salary based on experience Direct hire position with growth potential Be part of a team that values innovation, safety, and quality Ready to put your chemistry skills to work in a role where you can truly make a difference? Apply today and let’s start the conversation! A.R. Mazzotta is an equal opportunity employer. It is the policy of A.R. Mazzotta to employ, recruit, hire, train and promote individuals without regard to race, color, religious creed, sex, national origin, age, marital status, present or past history of mental disability, intellectual disability, learning disability, or physical disability, religion, political affiliation or belief, pregnancy, ancestry, veteran status, sexual orientation, gender identity or expression or any other status protected by federal, state, or local laws.

Chemist Risk Engineering - KR08LE We're determined to make a difference and are proud to be an insurance company that goes well beyond coverages and policies. Working here means having every opportunity to achieve your goals - and to help others accomplish theirs, too. Join our team as we help shape the future. The Risk Engineering Chemist is responsible for conducting chemical analysis on submitted samples following recognized and approved methods while maintaining conformance to rigid quality assurance requirements. This role involves developing and maintaining relationships with key stakeholders such as Agents & Brokers, Claims, Underwriting, and National accounts. Leveraging their analytical experience of laboratory functions and customer-focused consultations, the Risk Engineering Chemist provides differentiating service to our insureds and business partners across the organization. Additionally, the role includes innovating and operationalizing new technologies to create efficiencies, expand scope, and capabilities. This role will be based out of our Hartford, CT office and will require someone to be in the office Monday - Friday. Responsibilities: + Conduct chemical analysis on submitted samples following recognized and approved methods, maintaining conformance to rigid quality assurance requirements + Support Sr. Chemist/Forensic Chemist in analyses, project work, interpretation of data, providing assistance and support work. + Develop and maintain relationships with key stakeholders, providing consultation to field Risk Engineering staff, insured clients, and external fee clients concerning materials, methods, and analytical results + Participate in assigned projects, task groups, and duties of importance to the lab, the department, or the corporation + Comply with accreditation standards and maintain strict ISO standards, including review and updates to current methods and SOPs. + Conform to the safety and chemical hygiene plans of the laboratory and applies chemical hazard knowledge to all operations. + Perform sample login for IH samples/forensic evidence and maintain Chain of custody. + Ability to develop new laboratory methods to support the scope of analysis. + Identify and investigate analytical problems and questionable results. + Conforms to the safety and chemical hygiene plans of the laboratory and applies chemical hazard knowledge to all operations. + Familiar with the basics of the profession of industrial hygiene and basic industrial processes that create occupational health risk. + Willing to proactively contact clients and initiate discussions when beneficial to the customer. + Understand industrial hygiene equipment usage and able to assist virtually in providing training to clients. + Become a subject matter expert for chemistry-related topics as they relate to laboratory methods, analysis, and interpretation. + Maintain additional roles as outlined by Laboratory accreditation (Chemical Safety Officer, LIMS Specialist, Deputy QA Manager, Deputy Technical Manager). + Analytical recordkeeping up to date and in conformance to QA/QC policies. + Willing to accept and embrace diverse tasks beyond the scope of chemical analyses. + Train/participate with lab technologists on sample prep/login/media prep. + Understand and assist in IT-related laboratory systems such as LIMS systems and instrument software. Qualifications: + Four-year degree in applicable sciences with a B.S. and a minimum of 3 years of experience in related work. + Fully familiar with OSHA/NIOSH/ASTM sampling and analytical methods and any modifications unique to our lab. + Fully familiar with QA processes and exceptional attention to detail in all aspects. + Prepared to identify and investigate and analyze questionable results. + Willing to accept training from senior chemists and constructive criticism when offered. + Familiar with OSHA/NIOSH/ACGIH occupational exposure values and their inherent limitations. + Friendly, conversant nature recognizing the importance of the sample taker (the customer) to the laboratory. Compensation The listed annualized base pay range is primarily based on analysis of similar positions in the external market. Actual base pay could vary and may be above or below the listed range based on factors including but not limited to performance, proficiency and demonstration of competencies required for the role. The base pay is just one component of The Hartford's total compensation package for employees. Other rewards may include short-term or annual bonuses, long-term incentives, and on-the-spot recognition. The annualized base pay range for this role is: $65,600 - $98,400 Equal Opportunity Employer/Females/Minorities/Veterans/Disability/Sexual Orientation/Gender Identity or Expression/Religion/Age About Us (************************************* | Culture & Employee Insights (***************************************************** | Diversity, Equity and Inclusion (********************************************************* | Benefits (********************************************* Human achievement is at the heart of what we do. We believe that with the right encouragement and support, people are capable of achieving amazing things. We put our belief into action by ensuring individuals and businesses are well protected, and by going even further - making an impact in ways that go beyond an insurance policy. Nearly 19,000 employees use their unique talents in careers that span a variety of disciplines - from developing the latest technology to creating and promoting our products to evaluating future financial risks. We're also committed to programs that drive education and support volunteerism, which put human beings first. We do it because it's the right thing to do, and because when our customers, communities and employees succeed, we all do. About Us (************************************* Culture & Employee Insights (***************************************************** Diversity, Equity and Inclusion (********************************************************* Benefits (********************************************* Legal Notice (***************************************** Accessibility StatementProducer Compensation (************************************************** EEO Privacy Policy (************************************************** California Privacy Policy Your California Privacy Choices (****************************************************** International Privacy Policy Canadian Privacy Policy (**************************************************** Unincorporated Areas of LA County, CA (Applicant Information)

R10064220 Analytical Chemist (Open) KEY RESPONSIBILITIES: ➢ Perform routine chemical analysis of gas samples using analytical techniques such as chromatography and spectroscopy. ➢ Prepare and maintain accurate records of analytical data, including calculations and results. ➢ Assist with developing and validating new analytical methods, procedures, technologies, and equipment. ➢ Assist with installation of new systems as well as monitor and troubleshoot systems already deployed. ➢ Collaborate with team members to resolve technical issues related to analytical instrumentation and experimental procedures. ➢ Follow standard operating procedures and safety guidelines to ensure a safe working environment. ________________________Are you a MATCH? QUALIFICATIONS: ➢ Bachelor's degree in chemistry or related scientific discipline. ➢ 0-3 years experience working in a laboratory with analytical instrumentation. ➢ Familiarity with analyzers used in gas applications such as GC, FTIR, and NDIR. ➢ Proficiency in data analysis and interpretation using software tools like Excel and Google Sheets. Experience with statistical analysis is a plus. ➢ Strong critical thinking skills to solve performance-related problems in analytical systems. ➢ Excellent organizational and time management skills with the ability to prioritize tasks and meet deadlines. ➢ Strong written and verbal communication skills, with the ability to effectively present findings and collaborate with team members. REQUIREMENTS: ➢ Must have a strong understanding of fundamental principles of analytical chemistry and laboratory techniques. ➢ Must be able to work with systems that handle high pressure gasses. ➢ May require up to 25% travel to installation sites. ________________________ We care about and support our Airgas Families. This is evident not only through our competitive compensation but also through a comprehensive benefits package that includes medical, dental, and vision plans, vacation, sick time, floating holidays, and paid holidays for full-time employees. We provide a progressive parental leave package for our eligible Airgas parents, offering generous paid time off for the birth or placement of children, including 14 weeks of paid child birth benefit for birth mothers on leave, as well as paid parental leave benefits for other associates. Additionally, we offer our employees a 401k plan with company matching funds, tuition reimbursement, discounted college tuition for employees' dependents, and an Airgas Scholarship Program for dependent children. _________________________ Your differences enhance our performance At Airgas, we are committed to building a diverse and inclusive workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world. We welcome and consider applications from all qualified applicants, regardless of their race, gender, sexual orientation, religion, disability or any other protected characteristic. We strongly believe a diverse organization opens up opportunities for people to express their talent, both individually and collectively and it helps foster our ability to innovate by living our fundamentals, acting for our success and creating an engaging environment in a changing world. _________________________ Equal Employment Opportunity Information We are an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic. Please click here to view the EEO Know Your Rights poster and here to view the Pay Transparency Nondiscrimination poster. Airgas, an Air Liquide Company invites any applicant and/or employee to review the Company's written Affirmative Action Plan or Policy Statement. This plan or policy statement is available for inspection upon request. Airgas, an Air Liquide Company and its group of companies does not discriminate against qualified applicants with disabilities and is committed to providing reasonable accommodations to the known disabilities of such individuals so as to ensure equal access to benefits and privileges of employment. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact us by email at us-accommodationrequest@airgas.com. _________________________ California Privacy Notice

Boehringer Ingelheim is seeking a Scientist III/IV - a laboratory-based role within the Biopharmaceutics and Material Sciences department at our Ridgefield, CT facility. The Scientist will conduct oral drug product manufacturing activities and be independently responsible for the completion of batches. Additionally, he/she will investigate the root cause of manufacturing issues/delays due to mechanical failures and thereby accounts for proper maintenance of various manufacturing equipment. The Scientist will also extend ad-hoc support to global projects and be part of multidisciplinary team, serving as an acknowledged resource of oral drug product manufacturing and drug substance milling. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies´ success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim´s high regard for our employees. **Duties & Responsibilities** + Conducts various oral drug product manufacturing processes, including roller compaction, fluid bed granulation, tablet film coating, compression, and various milling operations for drug substances. + Thoroughly troubleshoots manufacturing issues related to mechanical or formulation aspects and strategize with vendor for proper maintenance and calibration of instruments. + Participates in and contributes to multidisciplinary project teams/sub-teams, and functions as an acknowledged resource in the field of expertise within and outside Material and Analytical Sciences (MAS). + Responsible for preparing and reviewing technical memos and reports. + Performs literature searches, maintains high level of expertise, learns and utilizes new techniques and technologies to enhance development capabilities; communicates progress via technical reports, presentations at scientific meetings and publications + Demonstrates sound of technical proficiency in field; trains junior level scientists/staff in this field + Reports and treats data with a high level of integrity and ethics + Complies with applicable regulations, BI policies/procedures and performing all work in a safe manner; Maintains proper records in accordance with SOPs and policies **Requirements: ***Candidate will be hired at level commensurate with experience and education***** + Extensive experience in pharmaceutical manufacturing processes of oral drug products including milling of drug substances. + Profound experience in troubleshooting of unit operations and resolving maintenance issues. + Adequate knowledge of characterization of both drug substance and drug product; able to act for supervisor in his/her absence + Strong ability to collaborate effectively with a team in a deadline-driven environment + Thorough knowledge and understanding of applicable regulations + May require an ability to push, pull, lift and carry objects up to 50lbs. + May require ability to wear a respirator **Requirements for Scientist III:** + Master´s Degree with three plus (3+) years or Bachelor´s Degree with seven plus (7+) years of solid oral formulation and process development experience in Pharmaceutical Industry. + Background from Chemistry, Physics, Pharmaceutical Sciences, Engineering or related scientific discipline. + Ability to operate laboratory equipment and systems with independence + Ability to draft technical reports + Concise and accurate reporting of technical data and interpretation thereof **Requirements for Scientist IV:** + Master´s Degree with six plus (6+) years or Bachelor´s Degree with ten plus (10+) years of solid oral formulation and process development experience in Pharmaceutical Industry. + Background from Chemistry, Physics, Pharmaceutical Sciences, Engineering or related scientific discipline. + Implements new experimental designs, strategies, explore new technologies, and independently design and execute studies. + Plan and conduct laboratory experiments and evaluate and interpret data + Provide training and guidance to junior staff + Prepare technical reports with minimal supervision, publications and oral presentations **Compensation Data** This position, Scientist III, offers a base salary typically between $90,000.00 and $147,000.00 USD. The position may be eligible for a role specific variable or performance based bonus and or other compensation elements. For an overview of our benefits please click here. (***************************************************************** **Eligibility Requirements** Must be legally authorized to work in the United States without restriction. Must be willing to take a drug test and post-offer physical (if required) Must be 18 years of age or older. All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.

Job Title: R&D Lab Technician Hours / Schedule: Monday - Friday, 8:00 am to 4:00 pm Type: Direct Hire Salary: $52K + bonus and generous benefits package! ENTRY LEVEL role! Will consider candidates graduating in May 2025! Chemistry & Biochemistry Degrees or Food Science background ideal! Responsibilities LAB TESTING EQUIPMENT + TOC (Total Organic Carbon) and TGA (Thermogravimetric Analysis) + Basic lab testing, such as: Density, Particle size, Moisture, Hardness LAB WORK + Understand basic lab safety, such as Personal Protective Equipment (PPE) and hazardous symbols. + Fundamental knowledge of Organic chemistries + Create laboratory samples and prototypes ranging from 50 to 500 grams. + Prepare dry or wet blends using: + Kitchen Blenders + Small rotary blends + Primarily handle non-hazardous chemicals utilized in nutraceuticals. + Work with some hazard substances such as solvents, acids, bases and higher concentration nutraceuticals (Vitamin D, Selenium) which do have hazards. + Take notes, formulate, and share test results with supervisors and team members + Ensure that inventory documents and Safety Data Sheets (SDS) for the laboratory or laboratories are properly maintained. + Follow instructions and, upon receiving full training, capable of creating directions for others to follow. + Maintain Lab cleanliness and organization + Maintain an adequate supply of lab equipment + Attend weekly R&D meetings + Collaborate with other departments, such as QC / QA, Regulatory, Sales + MS Excel and math skills needed PILOT WORK: + Knowledgeable and prepared to learn machinery for upscaling to 500 kilograms. PRODUCTION: + Observe how small concepts are developed into larger projects. + Assist with carrying 10-50 pound bags. + Understand the operational mechanisms of large equipment and distinguish them from those of smaller equipment. + Administrative duties: 10-15 hours per week. Requirements + Bachelor's Degree in Chemistry or Biochemistry (preferred), Pharmacy, Biology, Materials Engineering, Chemical Engineering or related science field + NOTE: Candidates who are graduating in May 2025 will be considered + 1-3 years' experience in a manufacturing environment is preferred. + Knowledge of GMP and QA/QC for the food industry. + Knowledge of raw materials used in the nutraceutical and natural products chemistry. + Knowledgeable in the basic types of unit operations used in chemical industries. + Working knowledge of the types of analytical methods used to characterize chemicals. + Practical experience solving problems related to typical chemical processing operations is especially desirable. Must be fluent in English. Benefits Our client provides a comprehensive benefits package. 8% of Gross W2 in 401(k) profit sharing, and generous health benefits. As this is a direct hire position with our client, System One benefits described below would not apply to this role. Benefits program listed above would be those applicable to this role. #M3 Ref: #558-Scientific System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Job Title: Quality Control (QC) Chemist FLSA Classification: Full-Time, Exempt Professional Work Hours: General Shift: 8:30AM â 5:00PM (may vary based on business needs) Reports To: Quality Control Manager Salary: $65,000 - $90,000 Purpose: The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education, training, experience or a combination of all three. Generally, modifier designation with respect to experience for Chemist are as follows. However, combination of education, training, and special skills will determine the assignment of Level to a specific individual: Scope: The scope (content and statements) of this is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual assigned basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role. Duties and Responsibilities The general duties and responsibilities of the "Chemist" include but are not limited to the following: * Conduct routine testing or other analysis in a specific group or department setting. * Conduct advanced testing and/or critical testing, as required. * Operate specialized equipment or conduct specialized skill testing * Working knowledge of raw materials testing and release * Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP * Lead investigation activities. * Ensure compliance to all data integrity and cGMP practices, procedures, and expect * Ensure compliance with all good documentation practices. * Other duties and responsibilities as assigned by the Head of the Department or Section Head Education and Experience * Bachelor's degree (BS or BA), physical sciences preferred * Proficiently speak English as a first or second language * Proficiently communicate and understand (read and write) scientific work in English * Have excellent organization, learning and teaching skills required to work in teams * Ability to understand and analyze complex data sets. * Working knowledge of Microsoft Office programs and other scientific based software. * Experience in Inhalation products (MDI) is a plus Working conditions This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or aroundsolvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required. Physical requirements * Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to10 kg, may be required. * Able to wear appropriate personal protective equipment at all times, when required. * Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period. Professional and Behavioral Competencies * Must be willing to work in a pharmaceutical packaging setting. * Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday. * Must be willing to work some weekends based on business needs as required by management. * No remote work available * No employment sponsorship or work visas. GLOBAL COMPANY Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in Indiaâs pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Ciplaâs focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.) About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited. EEO Statement Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

The Chemist is responsible for and has experience in performing chemical analysis for one of the assigned QC laboratories (Raw Material, Finished Product, Microbiology, ICP, Technical Support) which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. Responsibilities: Responsibilities include, but are not limited to: Follow all laboratory SOPs, including but not limited to laboratory safety, chemical handling and storage, gowning, equipment use, cGMP, GDP, data integrity, DEA requirements, etc. Perform routine laboratory chemical analysis on finished product, stability, raw material, and/or investigation samples, as assigned, using HPLC, UPLC, GC, UV-vis, FTIR, ICP, TOC and other wet chemistry techniques in accordance with the prescribed approved analytical test method. Maintain a clean and organized laboratory working environment. Dispose of used/expired/excess chemicals, solutions, solvents, etc. in dedicated waste receptacles. Report well-written, accurate and timely results. Review data, calculations, notebooks, and reports. Assist in laboratory investigations, as assigned. Assist in Cleaning, Method and Process validation testing and protocol/report review, as assigned. Assist in maintaining and troubleshooting laboratory equipment. Suggest improvements to existing testing methods when possible. Mentor and give guidance to entry-level personnel on techniques performed in the lab and assist with laboratory related questions as needed. Assist with routine Metrology functions, including instrument cleaning/ preventive maintenance/ calibration/ verification activities. Monitor and assist with maintaining proper inventory levels of all laboratory supplies. Assist with sample receiving, chemical inventory, document filing, housekeeping, etc. Other responsibilities as assigned by Management. Requirements Education and Experience: Bachelor's degree in a science related field. Between 1 and 9 years of work experience in a laboratory setting. Skills, Knowledge, and Abilities: Knowledge of laboratory chemistry and cGMPs. Proficient in Microsoft Word, Excel, graphs/charts and databases. Proficient in HPLC/UPLC, ICP, Dissolution, IR, UV/VIS, and wet chemistry testing. Proficient with analytical laboratory software. Able to multitask and meet tight deadlines. Excellent organizational skills with attention to detail. Able to effectively present results. Able to perform testing on many methods and troubleshoot minor method issues. May require some guidance/supervision as needed. Able to troubleshoot basic instrument issues independently and complex instrument issues under supervision. Physical Demands: Required to sit and stand for long periods of time. Frequently reaching with arms/hands up to 2 feet. Good hand eye coordination. Occasionally required to walk and kneel. Must be able to lift and/or move up to 50 pounds. Must be able to use close vision, distance vision, peripheral vision, color vision and the ability to adjust focus. Required to reach with arms and use hands and fingers to handle or feel objects, tools and computer controls. Required to stoop, kneel, crouch, stand, bend, sit, talk, hear, climb stairs. Work Environment: Work environment in laboratory and production operations facilities include close proximity to heavy machinery and pharmaceutical powders. Potential to move between production operations sites/areas to complete job functions. Employee work hours/schedule and/or shift are subject to change based on business needs and Management discretion. Required to be present in the laboratory to perform daily testing and collaborate with department director, manager, and peers. Responsible for compliance with all rules and regulations pertaining to safety policies with the proper attitude toward safety and health, helping to ensure that all department operations are performed with the utmost regard for the safety and health for all personnel. Supervisory Responsibilities: None Personal Protective Equipment or Attire Required for Position: Gowning as required by GMPs and/or SOPs. Pay Range: $50,000 - $80,000 per year

Adecco is currently assisting an American supplier of healthy hydration products in recruiting for a Product Development Scientist in Stamford, CT. Hybrid Schedule: Tuesdays, Wednesdays, and Thursdays in-office (flexible) **Pay Rate:** The wage for this position is between $60 and $65.51. Hourly wage may depend upon experience, education, geographic location and other factors. Be responsible for identifying technical solutions and delivering product formulation and scale up needs for the innovation and renovation project portfolio. + Lead consumer-focused new product/formula development projects for all domestic brands + Set and manage product development project plans and facilitate execution to ensure projects are completed on time and within budget + Hands on benchtop beverage development, scale up and industrialization + Collaborate cross-functionally with Marketing, Quality, Engineering, Purchasing, Regulatory and Legal while leveraging external resources from ingredient suppliers, co-manufacturers and other 3rd party resources to deliver project results and innovative new product formulations. + Lead the qualification of 3rd party flavor houses, develop RFP/Briefs for new flavor/ingredient opportunities. + Lead ingredient, product recipe and specification development deliverables through industrialization phase + Manage technical direction of projects; identify /communicate key deliverables and next steps. + Manage complex business relationships with ingredient, process technology partner companies, contract developers and manufacturers, consultants, vendors, cross-functional departments, and outside experts in support of achieving consumer needs and effective project execution. + Effectively prioritize and manage multiple projects concurrently varying in length. + Utilize the Primo Brands stage gate innovation framework to ensure full compliance with the Quality Management System and adhere to all relevant Primo Brands Technical Instructions for new product development initiatives. + Support on-going operations with recipe/ingredient specification changes and the qualification of new ingredients. **Qualifications** + Bachelor's degree required in Food Science, food engineering or related field + Minimum 7-10 years of relevant work experience in product development, process scale up, quality, or manufacturing in CPG setting (Beverage development highly preferred) + Strong project management experience with the ability to manage multiple projects concurrently and in matrix environments + Strong computer skills, including the use of Microsoft Word, Excel, Project, and PowerPoint as well as SAP + Understanding of financials (COGs, basic P&L understanding) + Six Sigma Certification, GSTD/DMAIC, FI experience a plus. + Ability to travel, approximately 15% throughout the year. Click on **_apply now_** for instant consideration! Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria. **Pay Details:** $60.00 to $65.51 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to ********************************************** The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: + The California Fair Chance Act + Los Angeles City Fair Chance Ordinance + Los Angeles County Fair Chance Ordinance for Employers + San Francisco Fair Chance Ordinance

**Who Are We?** Taking care of our customers, our communities and each other. That's the Travelers Promise. By honoring this commitment, we have maintained our reputation as one of the best property casualty insurers in the industry for over 160 years. Join us to discover a culture that is rooted in innovation and thrives on collaboration. Imagine loving what you do and where you do it. **Job Category** Product **Compensation Overview** The annual base salary range provided for this position is a nationwide market range and represents a broad range of salaries for this role across the country. The actual salary for this position will be determined by a number of factors, including the scope, complexity and location of the role; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. As part of our comprehensive compensation and benefits program, employees are also eligible for performance-based cash incentive awards. **Salary Range** $79,400.00 - $130,900.00 **Target Openings** 1 **What Is the Opportunity?** Product Development teams play a critical role in the achievement of Travelers financial objectives (growth, profit & retention) for one or more insurance products through the development, implementation and monitoring of product strategies and corresponding actions. As a Sr Analyst, Product Development, you will assist and implement analysis and evaluation of existing market and new product opportunities that deliver product development and product enhancements to the marketplace. In this role you will implement existing and new product solutions including monitoring and evaluating product performance and action plans. **What Will You Do?** + Execute and enhance existing product strategies and actions by collaborating and communicating with business unit stakeholders and management to achieve financial objectives. + Conduct high level market, competitor, and consumer research analysis to identify and recommend new products, markets and services or enhance existing ones. + Identify potential opportunities through root cause analysis and propose solutions. + Understand and assist with developing and implementing system and process solutions that align with the product's strategy. + Execute product enhancement work including launch and rollout plans related to established product strategies and action plans. Ensure strategies and plans address compliance needs and regulatory requirements. + Perform analysis by accessing and utilizing data to update recommendations on new or existing products. When appropriate, partner with data analytic teams to build support for recommendations. + Develop communication, training, and marketing materials in support of new or enhanced products and initiatives and may deliver training to stakeholders when appropriate. + Support the post implementation monitoring and measurement mechanisms for product strategies and initiatives in support of outlined success criteria. + Perform other duties as assigned. **What Will Our Ideal Candidate Have?** + Bachelor's Degree. + Three years of product development experience preferably in the financial services industry. + General knowledge of underwriting, coverage, rules, compliance/regulatory environment, and insurance financials. + Ability to think strategically and use judgment to resolve issues as they arise. + Strong data analysis skills with the ability to interpret trends and provide insights and recommendations to business partners. + Excellent communication skills with the ability to consult and present information effectively. + Experience working on cross-functional teams. + Have strong innovation skills including thinking critically about multiple perspectives and approaches to solving problems. + Demonstrated ability to interact and across levels and organizations, including consensus and team building. **What is a Must Have?** + Bachelor's Degree or equivalent combination of education and experience. + Two years of relevant experience with understanding and knowledge of insurance products. **What Is in It for You?** + **Health Insurance** : Employees and their eligible family members - including spouses, domestic partners, and children - are eligible for coverage from the first day of employment. + **Retirement:** Travelers matches your 401(k) contributions dollar-for-dollar up to your first 5% of eligible pay, subject to an annual maximum. If you have student loan debt, you can enroll in the Paying it Forward Savings Program. When you make a payment toward your student loan, Travelers will make an annual contribution into your 401(k) account. You are also eligible for a Pension Plan that is 100% funded by Travelers. + **Paid Time Off:** Start your career at Travelers with a minimum of 20 days Paid Time Off annually, plus nine paid company Holidays. + **Wellness Program:** The Travelers wellness program is comprised of tools, discounts and resources that empower you to achieve your wellness goals and caregiving needs. In addition, our mental health program provides access to free professional counseling services, health coaching and other resources to support your daily life needs. + **Volunteer Encouragement:** We have a deep commitment to the communities we serve and encourage our employees to get involved. Travelers has a Matching Gift and Volunteer Rewards program that enables you to give back to the charity of your choice. **Employment Practices** Travelers is an equal opportunity employer. We value the unique abilities and talents each individual brings to our organization and recognize that we benefit in numerous ways from our differences. In accordance with local law, candidates seeking employment in Colorado are not required to disclose dates of attendance at or graduation from educational institutions. If you are a candidate and have specific questions regarding the physical requirements of this role, please send us an email (*******************) so we may assist you. Travelers reserves the right to fill this position at a level above or below the level included in this posting. To learn more about our comprehensive benefit programs please visit ******************************************************** .

SCA Pharmaceuticals is a dynamic rapidly growing company consisting of passionate individuals who believe in our mission of providing high quality medications that are critical in saving and sustaining human life. SCA Pharma is an FDA 503B outsourcing facility providing customized medications for hospitals and healthcare facilities across the United States. We do this through unyielding quality, safety and integrity, our commitment to accountability and ownership, teamwork and creating better solutions by simplifying the complex. Summary: The Senior Analytical Scientist (Chemistry) is responsible for managing the lifecycle of analytical methods. This includes the development, validation, and verification of methods to ensure the potency and stability of drug substances and products, maintaining high standards of quality and compliance. The role requires adherence to USP-NF Compendial testing standards, creating comprehensive validation reports, and generating Standard Operating Procedures (SOPs). Essential Functions: Develop, validate, and verify USP-NF compendial testing for drug substances and drug products, ensuring compliance and reliability. Execute forced-degradation experiments to support method development and improve understanding of product stability. Write and execute method validation and verification protocols for UPLC/HPLC assays and other routine testing procedures, providing comprehensive reports. Conduct analytical method troubleshooting and lead discrepancy investigations to improve testing processes. Maintain strict adherence to USP-NF Compendial testing standards for injectable solutions and antibiotic standards, ensuring precise documentation. Develop and maintain Standard Operating Procedures (SOPs) related to chemical testing, ensuring clarity and regulatory compliance. Collaborate with the global Chemistry Team across sites on projects and continuous improvement initiatives, fostering innovation and teamwork. Performs other duties as assigned Requirements Required Qualifications & Experience: Bachelor's degree (in life sciences) 7+ years of Laboratory experience preferred Desired Knowledge, Skills, and Abilities: · Extensive experience in developing and validating UPLC/HPLC methods, particularly stability-indicating assays. · Strong proficiency in executing forced-degradation studies and analytical troubleshooting. · In-depth knowledge of USP-NF Compendial standards and regulatory requirements for chemical testing. · Excellent project management skills, with the ability to drive continuous improvement initiatives. · Proficient in MS Office Suite (Word, Excel, PowerPoint, Outlook). · Understanding of USP/FDA and ICH regulations related to method development, validation, and verification. · Communicate effectively with internal personnel, as well as external customers and vendors. SCA Pharma is an equal opportunity employer (Minorities/Females/Disabled/Veterans). We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, marital status, disability, veteran status, or any other basis protected by applicable federal, state, or local law.

Jobs for Humanity is collaborating with Upwardly Global and with Contract Pharmacal Corp to build an inclusive and just employment ecosystem. We support individuals coming from all walks of life. Company Name: Contract Pharmacal Corp Job Description Position Summary: Develop stability-indicating methods. Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. Responsibilities: Responsibilities include, but are not limited to: Knowledge of USP and FDA requirements. Develop stability-indicating methods for Active Pharmaceutical Ingredients (API) and Dietary Supplement products. Generate method validation protocols. Execute methods validation and methods transfer. Generate method validation reports and analytical methods. Design and conduct full analysis of Dietary supplements and Active Pharmaceutical Ingredients (API) products and their impurities. Conduct assay, content uniformity, dissolution, in-process blend, and blend uniformity of newly developed and stability samples in support of formulation and process development. Prepare result documentation for department and general review. Identify and resolve problems with analytical methods and provide troubleshooting on instrumentation. Conduct Performance Qualification (PQ) on various instruments. Provide leadership, guidance and hands-on training to new employees and provide technical support to other departments. Effectively communicate information in concise reports. Other responsibilities as assigned by Senior Management. Requirements: Education and Experience: Bachelor's degree in chemistry or analytical chemistry with 4-5 years of pharmaceutical experience OR Master's degree or Ph.D. in chemistry or analytical chemistry with 3-4 years of pharmaceutical experience Instrumentation and Computer Experience: Instrumentation: HPLC, UPLC, ICP, GC, FT-IR, UV, Dissolution, pH, TOC, and Karl Fischer. Computer programs: Empower 1-3, EZ Chrome Elite, WindLab, ChemStation, Microsoft Word, Excel, and Outlook. Work Conditions: Hours/Travel maybe subject to changed based on management/company discretion. Work location are subject to change as needed to meet business requirements. While performing the duties of this job, the employee is regularly required to stoop, kneel, crouch, stand, bend, sit, talk, hear or walk for long periods. The employee may lift and/or move up to 50 lbs. Specific vision abilities required by this job include close vision, distance vision, depth perception, and ability to adjust focus. Supervisory Responsibilities: None Personal Protective Equipment or Attire Required for Position: As needed Salary Range: $70,000 - $90,000 per year

At Sheffield Pharmaceuticals, the home of the original Sheffield Toothpaste, we offer exclusive, quality, branded products to promote wellness and relief to our customers. Our wellness and first aid products include a variety of creams and ointments, nasal products, and toothpaste all made in the USA since 1850. We are currently seeking a junior level quality focused QC Chemist with analytical or quality control laboratory experience in a Manufacturing environment. WORK HOURS: 3:30 PM - 12:00 AM M-F EDUCATION/EXPERIENCE: Bachelors degree in chemistry or related field. Minimum of one-year experience in analytical or quality control laboratory preferred. Passing of company required tests. WAGE CATEGORY: Non-Exempt DUTIES: Under direction from the Laboratory Supervisor, performs quality control analysis on any or all of the following samples: incoming raw materials in-process samples finished/filled products process validation/evaluation stability testing customer complaint Routine, repetitive checking and testing of production product, including visual and sample inspections of parts used, weights, and measures. Inspect production (compounding & filling) equipment for various Q.C. aspects. Maintain proper documentation for filling quality control as required Assists in experiments relative to the discovery and development of new products. Makes pilot batches of experimental products. Create processing batch sheets from work orders including: Allocation sheet -log W.O. into allocation book. Batch sheets-determine proper number of batches per mixing devise, check scratch program for batch size, check ingredient amounts and order of addition. QC sheet-insure QC requirements are in order. Method of MFG-print out appropriate Method of manufacturing. Create packaging batch records (PBR's), check artwork, crimp code, log sheets, & shipping requirements. Prepare artwork ingredient list. Complete Certificate of Analysis for customer orders. Send letters and samples to outside contract laboratories. Create Bulk labeling stickers. General electronic and hard copy file maintenance. Housekeeping with respect to records control. Maintain and update as needed the NS database and MSDS log. Maintain cleanliness and appearance of department. Assist in the disposal of hazardous (laboratory) waste Assist in laboratory instrument qualification and/or calibration Act as subject matter expert for laboratory instrumentation or analytical techniques Maintain proper liaison with all departments to contribute to the team philosophy. Responsible for following all safety regulations and complying with S.O.P.'s, DEP, EPA, OSHA, FDA, and cGMP's while performing duties. Other assigned tasks as necessary assigned by Management. Follow all Environmental and OSHA requirements. Attend in-house training sessions. Sheffield Pharmaceuticals is an Equal Employment Opportunity employer. We provide equal opportunity to employees and applicants for employment without regard to race, creed, color, religion, sex, age, national origin, physical or mental disability, sexual orientation, marital or familial status, genetic information, protected veteran status, or other basis protected by law.'

Who Are We? Taking care of our customers, our communities and each other. That's the Travelers Promise. By honoring this commitment, we have maintained our reputation as one of the best property casualty insurers in the industry for over 160 years. Join us to discover a culture that is rooted in innovation and thrives on collaboration. Imagine loving what you do and where you do it. Job CategoryProductCompensation Overview The annual base salary range provided for this position is a nationwide market range and represents a broad range of salaries for this role across the country. The actual salary for this position will be determined by a number of factors, including the scope, complexity and location of the role; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. As part of our comprehensive compensation and benefits program, employees are also eligible for performance-based cash incentive awards. Salary Range$79,400.00 - $130,900.00Target Openings1What Is the Opportunity?Product Development teams play a critical role in the achievement of Travelers financial objectives (growth, profit & retention) for one or more insurance products through the development, implementation and monitoring of product strategies and corresponding actions. As a Sr Analyst, Product Development, you will assist and implement analysis and evaluation of existing market and new product opportunities that deliver product development and product enhancements to the marketplace. In this role you will implement existing and new product solutions including monitoring and evaluating product performance and action plans.What Will You Do? Execute and enhance existing product strategies and actions by collaborating and communicating with business unit stakeholders and management to achieve financial objectives. Conduct high level market, competitor, and consumer research analysis to identify and recommend new products, markets and services or enhance existing ones. Identify potential opportunities through root cause analysis and propose solutions. Understand and assist with developing and implementing system and process solutions that align with the product's strategy. Execute product enhancement work including launch and rollout plans related to established product strategies and action plans. Ensure strategies and plans address compliance needs and regulatory requirements. Perform analysis by accessing and utilizing data to update recommendations on new or existing products. When appropriate, partner with data analytic teams to build support for recommendations. Develop communication, training, and marketing materials in support of new or enhanced products and initiatives and may deliver training to stakeholders when appropriate. Support the post implementation monitoring and measurement mechanisms for product strategies and initiatives in support of outlined success criteria. Perform other duties as assigned. What Will Our Ideal Candidate Have? Bachelor's Degree. Three years of product development experience preferably in the financial services industry. General knowledge of underwriting, coverage, rules, compliance/regulatory environment, and insurance financials. Ability to think strategically and use judgment to resolve issues as they arise. Strong data analysis skills with the ability to interpret trends and provide insights and recommendations to business partners. Excellent communication skills with the ability to consult and present information effectively. Experience working on cross-functional teams. Have strong innovation skills including thinking critically about multiple perspectives and approaches to solving problems. Demonstrated ability to interact and across levels and organizations, including consensus and team building. What is a Must Have? Bachelor's Degree or equivalent combination of education and experience. Two years of relevant experience with understanding and knowledge of insurance products. What Is in It for You? Health Insurance: Employees and their eligible family members - including spouses, domestic partners, and children - are eligible for coverage from the first day of employment. Retirement: Travelers matches your 401(k) contributions dollar-for-dollar up to your first 5% of eligible pay, subject to an annual maximum. If you have student loan debt, you can enroll in the Paying it Forward Savings Program. When you make a payment toward your student loan, Travelers will make an annual contribution into your 401(k) account. You are also eligible for a Pension Plan that is 100% funded by Travelers. Paid Time Off: Start your career at Travelers with a minimum of 20 days Paid Time Off annually, plus nine paid company Holidays. Wellness Program: The Travelers wellness program is comprised of tools, discounts and resources that empower you to achieve your wellness goals and caregiving needs. In addition, our mental health program provides access to free professional counseling services, health coaching and other resources to support your daily life needs. Volunteer Encouragement: We have a deep commitment to the communities we serve and encourage our employees to get involved. Travelers has a Matching Gift and Volunteer Rewards program that enables you to give back to the charity of your choice. Employment Practices Travelers is an equal opportunity employer. We value the unique abilities and talents each individual brings to our organization and recognize that we benefit in numerous ways from our differences. In accordance with local law, candidates seeking employment in Colorado are not required to disclose dates of attendance at or graduation from educational institutions. If you are a candidate and have specific questions regarding the physical requirements of this role, please send us an email so we may assist you. Travelers reserves the right to fill this position at a level above or below the level included in this posting. To learn more about our comprehensive benefit programs please visit *********************************************************

Formulation chemist needs Bachelor of Science or Master of Science in Chemistry, Biology, Engineering or related field Formulation chemist requires: Minimum 0-1 years of industry experience (Bachelor degree) Bachelor of Science or Master of Science in Chemistry, Biology, Engineering or related field Minimum 0-1 years of industry experience (Master degree) Great Computer skills Strong communication skills Travel to pilot facility in Trumbull, CT and manufacturing facility in Geneva New York Formulation chemist duties: Formulate hair related products under supervision of Senior Chemist or Manager. Understand, utilize and document within laboratory notebook and Enginuity every batch made with details of reason for the batch, batching notes, batch specification results and other test results as applicable. Understand, follow and adhere to project cost objectives and timelines for each project and develop cost estimates with supervisor. Follow requirements of the new product development process and follow through with action plans to meet the goals and timeline of the project. Conduct stability as required by department policy, i.e., track stability, update results charts and summarize data for review at each test period. Design and develop, as well as conduct efficacy testing, as required for projects and requested by supervisor - Co-ordinate Salon Testing; Design & conduct laboratory efficacy, field and claims tests and write reports detailing experiments, and analysis and summary of results. Co-ordinate Microbiological and Safety Testing. Communicate formulation stability and efficacy results and issues promptly and thoroughly as well as make recommendations for change/improvements when stability or efficacy testing fails. Interact with raw material vendors and other industry representatives to further expand on the understanding of their products, technologies and services.

The Associate Scientist is responsible for providing scientific support for the measurement product portfolio. They will provide scientific input to some aspects of the business including projects/orders, proposals, and solutions. This includes but is not limited to: working closely with hardware and software engineering in the development of solutions and in the execution of projects; assisting in responding to technical inquiries; contributing technical input in support of developing requirement specifications for new proposals and projects; independently analyzing the performance and application of existing and new analysis techniques; writing test procedures and providing documentation; presenting results to internal and external audiences. The Associate Scientist is regarded within the company as someone conversant in at least one or two application areas. WHAT MAKES A GREAT ASSOCIATE SCIENTIST? With an insatiable curiosity, you will learn all you can about the products and technologies in and around the products you work on. You will have a good understanding of balancing investigation with completing your tasks on time and within budget. You balance learning from more senior scientists with the process of self-exploration. You are always seeking to learn about the products and the industry. You will search for your niche and thrive there. You are developing a firm grasp of the organization and how to navigate and coordinate with any group or department. You have a sense of responsibility to deliver within expectations and you communicate well with others in all aspects of your role. RESPONSIBILITIES & DUTIES * As an Associate Scientist you are expected to work on at least two concurrent projects with guidance. * It is your responsibility to maintain and grow your application knowledge through both formal and informal on-the-job training and development. * You are expected to become an SME in at least one application area within 3 years. SKILLS & KNOWLEDGE The successful Associate Scientist will possess the following skills: * Basic understanding of radiation detection and measurement equipment. * Solid grasp of mathematics and statistical concepts. * Experience in programming, python or C++ is preferred; willingness to learn is necessary. * Excellent oral and written communication skills. EDUCATION & EXPERIENCE * Minimum BS or equivalent in Science or Engineering. * MS or equivalent in Science or Engineering can equate to 2 years of experience. * An Associate Scientist should have a minimum of 2 years of experience in a relevant application.