Chemist Jobs in Bexley, OH

Nutrition R&D Technician - Medical Device Industry Responsibilities: Collect and tabulate data for research projects Weigh ingredients and batch formulations Collect and submit samples for lab testing Perform pH and moisture analyses Skills: Knowledge of Food Science, Chemistry, or Microbiology Experience in a lab setting Strong analytical and math skills Requirements: Bachelor's degree in Food Science 0-3 years of experience 100% onsite role

Chemist II 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 and long-term incentive plans. Category/Shift: Salaried Full-Time Physical Location: 13307 Industrial Parkway Marysville, OH 43040 The Job You Will Perform: The Chemist II position is in the International Paper ink lab, which is part of the Enhanced Graphics division within the Custom Packaging and Display group. IP Ink supplies water based flexographic printing inks and related services to corrugated packaging converters, bag manufacturers, and other flexographic printers within International Paper and to external customers. The ink lab provides color matching, technical service, formulation, and research and development services to our customers in order to help them produce high quality packaging products. The Chemist II reports to the Lab Manager. * Responsible for product improvement, new product development, raw material evaluation and other lab functions as necessary * Coordinate and plan projects with Lab Manager and Chemist III * Conduct applicable lab testing, maintain project files and reports * Maintain a Laboratory Notebook * Maintains test chemical inventory. * Operate all laboratory testing equipment. * Identify proper vehicle system for given application. * Identify/recognize a customer's environmental restrictions and formulate accordingly. * Make proper anilox selection per machine requirements. * Provide color match and customer service support as needed * Conducts Chemical Approval process for new items * Schedules and participates in field-testing for new and/or improved products. May involve offsite travel * Responsible for specific manufacturing and R&D laboratory instrument maintenance and/or repair. * Participates in training and continuing education activities related to the job * Creates procedures and related SOP's for manufacturing and R&D. * Completes all required tasks and responsibilities while adhering to Specialty Products Safety Standards. * Initiates and implements cost saving projects. * All other duties assigned. * Participates in IPs ongoing 5S program * Generate best color match within cost constraints. * Works directly with vendors on R&D and complaint resolution. The Qualifications, Skills and Knowledge You Will Bring: * 4-year degree in Chemistry or related discipline, and 2+ years' experience in ink formulation/testing or related industry is preferred. * Industry related experience is desirable: Ink, paint, printing, or coatings. * Ability to travel up to 25%. * Previous experience with color or color matching and knowledge of industrial batch process and equipment is desired. * Strong technical/customer support skills. You will be required to work closely with sales, technical service and our customer base in a wide array of situations * Proficient in Microsoft Office applications (Word, Excel) * Ability to self-start, remain calm in stressful situations, and have a positive outlook are beneficial to this position. * Proficiency with Batchmaster Enterprise * Ability to communicate well verbally, and across electronic platforms such as e-mail, text, and instant messaging 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 Career You Will Build: Sales and Leadership training, promotional opportunities within a global company 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 125 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 a global producer of sustainable packaging, pulp and other fiber-based products, and one of the world's largest recyclers. Headquartered in Memphis, Tenn., we employ approximately 39,000 colleagues globally who are committed to creating what's next. We serve customers worldwide, with manufacturing operations in North America, Latin America, North Africa and Europe. Net sales for 2023 were $18.9 billion. Additional information can be found by visiting internationalpaper.com. International Paper is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. International Paper complies with federal and state disability laws and makes reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact reasonable.accommodations@ipaper.com or ************** Share this job: Location: Marysville, OH, US, 43040 Category: Technology Date: Mar 26, 2025 If you are not finding suitable opportunities, please click below to join our talent community! Join Our Community Nearest Major Market: Columbus Nearest Secondary Market: Dublin

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers . If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. Intertek is searching for a Chemist to join our Electrical team in our Columbus, Ohio office. This is a fantastic opportunity to grow a versatile career in Chemistry and Engineering! Intertek's Electrical business line applies more than 100 years of product testing expertise to quickly and efficiently help clients meet safety, performance, environmental and quality requirements for every market. Spanning a wide range of industries such as Medical, Lighting, Renewable Energy, HVACR, Appliances & Electronics, Hazardous Locations, Industrial Equipment, Life Safety & Security, IT & Telecom Equipment, Intertek's global network of laboratories employ world-class experts in their fields who deliver quality, accurate testing and certification that continually exceeds our clients' expectations and helps to clear a path for their product's success. Intertek is continually innovating and evolving to reduce risk for consumers, brands and organizations in every sector and industry around the world. We go beyond Testing, Inspection and Certification of products: we are a Total Quality Assurance Provider to industries worldwide. Intertek is continually innovating and evolving to reduce risk for consumers, brands, and organizations in every sector around the world. Our purpose: Bringing quality, safety, and sustainability to life. What are we looking for? The Chemist I position is responsible for Refrigerant Gas Detector Testing Program and will perform analytical testing on materials, gases and liquids per various industry test methods relating to the HVAC, Sanitation and Life Safety Salary & Benefits Information Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons. In addition to competitive compensation packages, Intertek employees are eligible for a variety of benefits including paid holidays. When working with Intertek, you can expect a benefit package competitively placed within the local market, including medical, dental, vision, life, disability, 401(k) with company match, generous vacation / sick time (PTO), tuition reimbursement and more. What you'll do: Set up test apparatus Test routine refrigerant samples and review reports relating to AHRI 700 refrigerant analysis. Test Samples to industry Methods such as ASHRAE 60335-2-40 Annex LL Perform Chemical compatibility evaluations on materials, additives and lubricants per ASHRAE 97, ASHRAE G38, UL157 and other related standard test methods Prepare “Round Robin” refrigerant samples and conduct analysis in support of AHRI certification programs Calibrate and maintain analytical equipment Assist with drafting non-standard test procedures for various R&D projects Conduct testing on chemically related quoted projects and maintain project files Conduct chemical compatibility and performance evaluations of pool and spa components and controllers per NSF 50 Construction Review and Gap analysis of refrigerant gas detectors to industry standards Write Recognition Reports for Refrigerant gas detector models Preform other duties as required This position outline is a general guideline and does not represent all encompassing details. The position assumes that the incumbent has both the mental and physical requirements to carry out the above defined duties. Additional Qualifications/Responsibilities Minimum Requirements & Qualifications: 4-year degree in chemistry or other related science field Knowledge of refrigerant testing and detector technology Ability to interpret standard language and develop test methods Ability to travel up to 15% as required by the role A valid driver's license and reliable driving record

Intertek is searching for a Chemist to join our Electricalteam in our Columbus, Ohio office. This is a fantastic opportunity to grow a versatile career in Chemistry and Engineering! Intertek's Electrical business line applies more than 100 years of product testing expertise to quickly and efficiently help clients meet safety, performance, environmental and quality requirements for every market. Spanning a wide range of industries such as Medical, Lighting, Renewable Energy, HVACR, Appliances & Electronics, Hazardous Locations, Industrial Equipment, Life Safety & Security, IT & Telecom Equipment, Intertek's global network of laboratories employ world-class experts in their fields who deliver quality, accurate testing and certification that continually exceeds our clients' expectations and helps to clear a path for their product's success. Intertek is continually innovating and evolving to reduce risk for consumers, brands and organizations in every sector and industry around the world. We go beyond Testing, Inspection and Certification of products: we are a Total Quality Assurance Provider to industries worldwide. Intertek is continually innovating and evolving to reduce risk for consumers, brands, and organizations in every sector around the world. Our purpose: Bringing quality, safety, and sustainability to life. What are we looking for? The Chemist I position is responsible for Refrigerant Gas Detector Testing Program and will perform analytical testing on materials, gases and liquids per various industry test methods relating to the HVAC, Sanitation and Life Safety Salary & Benefits Information Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons. In addition to competitive compensation packages, Intertek employees are eligible for a variety of benefits including paid holidays. When working with Intertek, you can expect a benefit package competitively placed within the local market, including medical, dental, vision, life, disability, 401(k) with company match, generous vacation / sick time (PTO), tuition reimbursement and more. What you'll do: Set up test apparatus Test routine refrigerant samples and review reports relating to AHRI 700 refrigerant analysis. Test Samples to industry Methods such as ASHRAE 60335-2-40 Annex LL Perform Chemical compatibility evaluations on materials, additives and lubricants per ASHRAE 97, ASHRAE G38, UL157 and other related standard test methods Prepare "Round Robin" refrigerant samples and conduct analysis in support of AHRI certification programs Calibrate and maintain analytical equipment Assist with drafting non-standard test procedures for various R&D projects Conduct testing on chemically related quoted projects and maintain project files Conduct chemical compatibility and performance evaluations of pool and spa components and controllers per NSF 50 Construction Review and Gap analysis of refrigerant gas detectors to industry standards Write Recognition Reports for Refrigerant gas detector models Preform other duties as required This position outline is a general guideline and does not represent all encompassing details. The position assumes that the incumbent has both the mental and physical requirements to carry out the above defined duties. Minimum Requirements & Qualifications: 4-year degree in chemistry or other related science field Knowledge of refrigerant testing and detector technology Ability to interpret standard language and develop test methods Ability to travel up to 15% as required by the role A valid driver's license and reliable driving record Intertek Total Quality Assured Intertek is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts. With passion, pace, and precision we work to exceed our customers' expectations, while engaging with our employees to be 10X in their performance and professional growth. Intertek is a drug-free workplace. For certain safety-sensitive roles, a pre-employment drug screen will be required. Based on local law and legislation, marijuana may be included in that screening. We Value Diversity Intertek's network of phenomenal people are our greatest assets, and the diversity they bring fuels our success. Intertek is an Equal Employment Opportunity Employer that values inclusion and diversity. We take affirmative action to ensure all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected characteristics. For individuals with disabilities who would like to request accommodation, or who need assistance applying, please email ******************* or call ************** (option #5) to speak with a member of the HR Department. #LI-DNP * Intertek does not accept unsolicited approaches from agencies and will not pay a fee for any placement resulting from the receipt of an unsolicited resume.Intertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification (ATIC) solutions for our customers' operations and supply chains. Working at Intertek means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustainability to life.

Position: Full-Time Total Rewards: Benefits/Incentive Information If you've worn a pair of glasses, we've already met. We are a global leader in the design, manufacture, and distribution of ophthalmic lenses, frames, and sunglasses. We offer our industry stakeholders in over 150 countries access to a global platform of high-quality vision care products such as the Essilor brand, with Varilux, Crizal, Eyezen, Stellest and Transitions, iconic brands that consumers love such as Ray-Ban, Oakley, Persol and Oliver Peoples, as well as a network that offers consumers high-quality vision care and best-in-class shopping experiences such as Sunglass Hut, LensCrafters, and Target Optical, and leading e-commerce platforms. Our unique business model and relentless pursuit of operational excellence ensures that consumers everywhere have access to products. Balancing speed, efficiency and proximity, the Company manages a global supply chain with cutting-edge technology, based on centralization for frames and on a capillary network for lens finishing and prescription laboratories. In our dynamic environment, fueled by technology and innovation, our people have the space to pioneer new solutions. Join our global community of over 200,000 dedicated employees around the world in driving the transformation of the eyewear and eyecare industry. Discover more by following us on LinkedIn! GENERAL FUNCTION Entry-level role in the kilogram-scale manufacture of specialty chemicals, including dyes and dye intermediates for use by both internal and external customers. MAJOR DUTIES AND RESPONSIBILITIES Specialty chemical production on kilogram scales Chemical apparatus set-up, reactor loading (solvents, raw materials) and unloading Chemical process monitoring and control Product purification (crystallization, chromatography, rotary evaporation, solvent recovery) Spectroscopy (ultraviolet, visible, infrared) Quality control Record keeping (Laboratory notebooks, Certificates of Analysis) Reporting (Standard Operating Procedures, Production reports) Compliance with safety and environmental regulations (OSHA, EPA) and internal practices BASIC QUALIFICATIONS Bachelor's degree in chemistry, chemical engineering, or related field Certifications: None required University research experience Familiarity in handling chemicals and chemical equipment Familiarity with running analytical instruments including GC, UV/Vis spectrometers Familiarity with Microsoft Office applications Excellent oral and written communication skills PREFERRED QUALIFICATIONS Bachelor's degree, Organic Chemistry with 1-2 years of industrial experience Experience in handling chemicals and chemical equipment on kilogram scales Experience in maintaining spectrometers and interpreting spectra Experience with maintaining analytical instruments including GC, UV/Vis spectroscopy Familiarity with SciFinder and SAP Employee pay is determined by multiple factors, including geography, experience, qualifications, skills and local minimum wage requirements. In addition, you may also be offered a competitive bonus and/or commission plan, which complements a first-class total rewards package. Benefits may include health care, retirement savings, paid time off/vacation, and various employee discounts. Upon request and consistent with applicable laws, EssilorLuxottica will provide reasonable accommodations to individuals with disabilities who need assistance in the application and hiring process. To request a reasonable accommodation, please call the EssilorLuxottica SpeakUp Hotline at ************ (be sure to provide your name and contact information so that we may follow up in a timely manner) or email ********************************. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, national origin, social origin, social condition, being perceived as a victim of domestic violence, sexual aggression or stalking, religion, age, disability, sexual orientation, gender identity or expression, citizenship, ancestry, veteran or military status, marital status, pregnancy (including unlawful discrimination on the basis of a legally protected pregnancy or maternity leave), genetic information or any other characteristics protected by law. Native Americans in the US receive preference in accordance with Tribal Law. .job Title{ display:none !important; } Nearest Major Market: Columbus Job Segment: Supply Chain, Social Media, Supply, Ophthalmic, Operations, Marketing, Healthcare

Job Title: R&D Chemist Department: Research & Development Last Reviewed: February 2025 Meridian Adhesives Group is a rapidly growing, full service global adhesive solutions provider, specializing in adhesive technologies used in electronics, industrial, and infrastructure applications. Fueled by a series of strategic acquisitions since its formation in 2018, we have established ourselves as an adhesive technology leader for a broad, global, blue-chip customer base comprised of OEMs, distributors, and industrial clients with an expanding global footprint. Guided by our core values-Safety & Sustainability, Respect, Integrity, Accountability, and Teamwork-we are driven to make a meaningful impact in everything we do. When you join Meridian, you become part of a dynamic team that values diverse perspectives, fosters professional growth, and encourages bold ideas. We're committed to creating a supportive environment where you can thrive, grow, contribute to groundbreaking projects, and help shape the future of our industry. Meridian Adhesives Group does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. Summary The Chemist will play a key role in the formulation, development, and testing of adhesive materials. Reporting to the R&D Manager, this position involves hands-on research, product development, and laboratory testing to support the company's innovative efforts and market-driven solutions. The Chemist will collaborate closely with cross-functional teams, ensuring new products meet technical requirements, performance expectations, and regulatory standards. Salary Range & Benefits $70,000 - $75,000 + 10% annual performance bonus target Health, dental, and vision insurance. 401(k) matching plan. Flexible spending account. Health savings account. Life, short-term and long-term disability insurance. Parental leave. Referral program. Paid time off. Paid holidays. Duties & Responsibilities Conduct research and development of new adhesive formulations and product enhancements. Perform laboratory testing to evaluate material properties, product performance, and stability. Analyze and interpret data, documenting results and preparing technical reports. Support scale-up and commercialization of new products, working closely with manufacturing and quality teams. Maintain an in-depth understanding of raw materials, formulation chemistry, and application methods. Collaborate with sales and technical teams to provide customer support, including troubleshooting and recommendations. Ensure compliance with safety, quality, and regulatory standards in laboratory operations. Maintain laboratory equipment, coordinate maintenance, and ensure proper documentation of experiments and findings. Stay up to date on industry trends, new technologies, and competitive products. Skills & Abilities Strong analytical and problem-solving skills with attention to detail. Hands-on experience with formulation, testing, and analytical instrumentation. Ability to interpret technical data and translate findings into actionable solutions. Excellent communication skills, both written and verbal, with the ability to work collaboratively. Strong organizational and time management skills, with the ability to manage multiple projects. Knowledge of regulatory requirements and testing protocols relevant to adhesives and electronic materials. Occasional travel to customer sites. Education & Experience Bachelor's degree in Chemistry, Chemical Engineering, or a related technical field. 2-5 years of experience in formulation chemistry, R&D, or a similar role. Experience with adhesives, coatings, or polymer-based products is highly preferred. Proficiency in MS Office (Excel, Word, PowerPoint, Outlook). Physical Requirements Prolonged periods of sitting at a desk and working on a computer. Additionally, prolonged periods of standing and working at a lab bench. Must be able to lift up to 15 pounds at times. The company is an Equal Opportunity Employer, drug free workplace, and complies with ADA regulations as applicable.

CAS uses intuitive technology, unparalleled scientific content, and unmatched human expertise to help companies create groundbreaking innovations that benefit the world. As the scientific information solutions division of the American Chemical Society, CAS manages the largest curated reservoir of scientific knowledge, and for 117 years, has helped innovators mine, assess and apply that information to keep businesses thriving. The CAS team is global, diverse, endlessly curious and strives to make scientific insights accessible to innovators worldwide. CAS is currently seeking a Food/Feed Scientist on our Content Operations team. This position is located at our headquarters in Columbus, Ohio Position Summary The Food/Feed scientist applies scientific expertise, analytical skills, problem solving capabilities, and relevant language skills to help build CAS's world-class collection of scientific data. Primary responsibilities include leveraging scientific and technical knowledge to curate high-quality research data from patent and journal literature in the Life Sciences content area in a production environment. The incumbent may also provide scientific and content knowledge, capabilities, insights, and solutions for other CAS functions. Additional responsibilities may include identifying and implementing process improvements, planning, managing, and participating in unit-level projects. The successful candidate will be an excellent team player who is organized and willing to adapt to the needs and requirements of an agile organization. This candidate must demonstrate a proactive and flexible attitude, with a keen willingness to show initiative. Requirements: * An advanced degree in Food science, Food chemistry, Biochemistry, or related scientific field. A bachelor's degree with extensive professional experience will be considered. * Professional experience with food or feed chemistry a plus * Excellent scientific reading comprehension and writing skills. * Solid analytical and problem-solving skills. * Ability to work independently as well as part of a team. * Ability to learn policies, work habits, insights, and tool usage from trainers to foster quality and productivity. * Effective organizational skills, including attention to detail, time management, and multi-tasking. * Familiarity with video conferencing, instant messaging, email, calendar scheduling, word processing, spreadsheets, and document sharing software. * Japanese, Korean, or other language skills a plus CAS offers a competitive salary and comprehensive benefits package, including a generous vacation plan, medical, dental, vision insurance plans, and employee savings and retirement plans. Candidates for this position must be authorized to work in the United States and not require work authorization sponsorship by our company for this position now or in the future. EEO/Minority/Female/Disabled/Veteran

INEOS Composites US LLC INEOS is a global manufacturer of petrochemicals, specialty chemicals and oil products. Our products touch every aspect of modern life. INEOS comprises 36 businesses each with a major chemical company heritage. Our production network spans 194 sites in 29 countries throughout the world. INEOS Pigments produces TiO2 and TiCI4 via the chloride process with approximately 500 employees at the Ashtabula Complex and 30 employees associated with the Baltimore Administrative and Technical Center (BATC). The T&I group is split between the Ashtabula Complex and the Baltimore Administration and Research Center (BATC). This role is a salaried, exempt position based in either BATC or Ashtabula with regular travel between the two sites. Future relocation to Columbus, OH will be required. The Scientist II receives supervision from T&I VP or Senior Scientist on a fortnightly or monthly basis and works week to week independently or as part of a team as required to apply chemical principles in synthesis and characterization of solid-state metal oxide materials leading to new or improved TiO2 pigment products. Carries out laboratory work on a day to day basis unsupervised. The role exists within the Technology & Innovation Group (T&I) and consists of material synthesis, characterization, and applications testing. The individual should also be able to improve and modify existing test methods that will benefit productivity as well as maintain laboratory equipment and laboratory order and make recommendations to improve laboratory work processes This position will apply good laboratory practices in following standard operating procedures as directed by the VP of T&I. Familiarity with the research tools in product development and quality testing required. The qualified individual should be able to take learning from the lab experiment or plant trial results and apply that to development of ideas for new product or improvement of current product and/or processes. This position will work with other T&I teams as well as the Manufacturing teams to achieve the performance goals needed for scale up at the Ashtabula Complex by conducting lab, pilot, and plant trials. The incumbent should possess critical analytical skills and be adept at utilizing solid decision-making tools coupled with a high level of data analysis skills. Key Activities: · Adhere to INEOS Pigments Safety Principles and Life Saving Rules · Complete Action Items on time · Complete computer-based training on time · Perform specific Safety Audits · Participate in safety improvement efforts including monthly meetings · Receives direction from the VP, T&I but works independently on a day to day basis. · Perform area inspections and keep laboratory chemical inventory current · Performs duties according to established standard operating procedures. · Maintains labs to ensure continued reliability use in development and evaluation efforts. · Understanding and experience in applications testing related to the TiO2 pigment markets helpful. · Will be responsible for ensuring all test procedures are carried out day to day · Order chemicals and supplies for experiments and to maintain inventory · Prepares samples, characterizes products, and formulates into end uses · Maintains good records and regularly reports study results Education and Experience: · A BS/BA degree in Chemistry, Chemical Engineering, or equivalent with 3-7 years industrial experience or equivalent · Good written and verbal presentation skills · Statistical accumen showing ability to organize, analyze, and interpret data · A good knowledge of Health and Safety procedures generally as relates to internal SHE and CHP guidelines · Should be well versed in pigment test methodologies. · Should be adept at performing surface treatments involving corrosive and caustic materials dissolved in water · Should have an excellent understanding of pigment manufacture. · Should have an excellent understanding of material characterization techniques. · Has a basic understanding of the operating principle of, and be able to perform regular maintenance of lab equipment. · Skilled at working with hands · Should be aware of TiO2 pigment market, customers and general regulations related to coatings, plastics and paper applications. · A good knowledge of pigment application testing and product awareness. · An awareness of the latest techniques, applications and analytical techniques for TiO2 pigment. · Should have demonstrated good interpersonal skills with peers · Should be available for plant trial support as required. · Should have a sense of how regulatory rules impact work functions Candidates must be authorized to work in the US and future sponsorship is unavailable for this role.

Major Responsibilities : Responsible for implementing and maintaining the effectiveness of the quality system. · Weighs ingredients, prepares batches, and supports production at the product research center · Submits samples for analysis and consolidates/tabulates results · Organizes non-routine testing, completes these tests and summarizes results B.S. in Food Science and Technology, Chemistry or Sciences preferred. 0 - 3 years technical work experience, preferably in developing food/nutritional products The candidate should also demonstrate the ability to handle multiple priorities as well as a good work ethic Qualifications B.S. in Food Science and Technology, Chemistry or Sciences preferred. 0 - 3 years technical work experience, preferably in developing food/nutritional products Additional Information Thanks & Regards ________________________________________________________________________ ___ Riya Seth | Team Recruitment | Mindlance, Inc. | W: ************

About Forge Forge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table, helping to champion teams that are navigating the long road from the lab bench to the bedside. Our goal is simple but vital to patients living with disease, and we take it seriously. With a patient-first approach, we are forging new models for working together to better accelerate these transformative medicines to reach those who need them the most. About The Team Manufacturing Science and Technology is a team of highly skilled Scientist responsible for the technology transfer of processes developed by Process Development into the GMP Manufacturing area. They are responsible for technical and scientific support for existing clients and internal production. The Manufacturing Science and Technology team develops and implements robust technology transfer, provides data analytics for existing processes and supports continuous improvement of cGMP Manufacturing. Manufacturing Science and Technology interacts with clients through the generation of reports, risk assessments and face to face meetings. About The Role We are currently seeking a Associate Scientist II, Manufacturing, Science & Technology (MS&T) to join the Forge Biologics Team. This is an exciting opportunity to support the MS&T strategy for a Cell & Gene Therapy Contract Development and Manufacturing Organization (CDMO). This includes supporting the development, implementation, and maintenance of all MS&T activities for cell & gene therapy products. As a Associate Scientist II in MS&T, you will be responsible for the successful transfer of viral vector processes into GMP production. What You'll Do (Responsibilities) Assist Technology transfers from Product Development to Manufacturing. Working with MS&T Scientists defining critical quality attributes, process parameters and conditions of critical importance to manufacturing under cGMPs. Collaborate closely with cross-functional teams, including clients, Client Development, Technical Sales, Process Development, Manufacturing, Quality, and Program Management, to ensure GMP readiness and provide technical expertise throughout the process Assist with client-facing functional Lead for Process Technology Transfers by performing detailed review of clients and Process Development process and generates technology transfer documents Support to General Manufacturing Practices (GMP) execution of the new processes and any deviation investigations, Corrective Action Prevention Plans (CAPAs), and necessary change controls Provide support for GMP execution, deviation investigations, CAPAs, and change controls Perform process monitoring (manufacturing data analysis, summary, and presentation), assist with campaign summary reports. Provides Product Development and Manufacturing with opportunities for process optimization and efficiency enhancements platform manufacturing process. Recommends improvements for MS&T practices and procedures Ensure all MS&T activities are in compliance with applicable regulatory requirements, including FDA, cGMP, and international regulatory requirements Support the development of related documents such as process development plans, manufacturing batch records, and SOPs Tracks progress of routine manufacturing and tech transfer projects against schedule, provides routine updates and proactively identifies operational risks and remediation. Investigate new technologies and techniques to reduce costs, improve timelines, enhance safety, and improve regulatory compliance. What You'll Bring (Qualifications) Master's degree in biology, molecular biology, virology, biochemistry or related discipline, or Bachelor's degree with 2+ years' relevant experience Proven track record in supporting MS&T teams Knowledge of FDA, cGMP, and international regulatory requirements Excellent communication, organizational, and interpersonal skills Strong problem-solving, decision-making, and leadership skills Work Environment and Physical Demands This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned. Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Life at Forge We are a team of diverse, driven and passionate people working together to trailblaze a new model for how we make medicines to treat patients with genetic diseases. Our team members use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services in the industry. Forge's core values lay the foundation for H.O.P.E. It provides us a common purpose that we all understand, work towards and live by. HARDWORKING - We work hard and smart, making a persistent and determined effort toward success. Working hard, with focus and desire is the key. OPEN - We strive to be approachable, actively listen and encourage others to contribute and speak up. We positively offer and receive constructive feedback. PURPOSE DRIVEN - We are passionate about working towards and delivering on our mission to manufacture gene therapies. ENGAGED - We are fully absorbed by and enthusiastic about our work and take positive action to further Forge's vision, mission and goals. We've Got You Covered We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly UnFORGEttable. Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents Flexible PTO (plus 14 paid company holidays) Annual bonus for all full-time employees 401(K) company match Fully-stocked kitchen with free food/drinks 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care Employee Assistance Program Wellness benefits (financial planning services, mental health counseling, employer paid disability) Professional & Personal development resources - LinkedIn Learning, a dedicate training staff in-house, mentoring opportunities & access to leadership development coaches

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details We are building a new chemistry lab to test the products in our packaging. This Quality Control (QC) Chemist II role will be creating the required documentation needed for the lab in preparation for initiating in-house testing. This QC Chemist II will focus on method development and validation testing, as required, of products repackaged at AHP. The QC Chemist II will also assist in troubleshooting methods and OOS investigations for the chemistry lab. As time allows they will also assist in stability and release testing, as necessary, and work closely with other departments within the Quality Unit to ensure drug product meets all standards. Ensure stability and release testing activities are compliant with FDA, DEA, other regulatory body requirements as applicable. Ensure compliance with local and corporate policies and procedures. Perform method development and validation testing for AHP repackaged products. Perform troubleshooting and assist with OOS investigations. Perform stability and release testing for drug products in accordance with compendial and global requirements, as applicable. Develop, revise, and review standard operating procedures (SOPs), work instructions (WIs), and test method documents to ensure compliance with applicable compendia and regulations. Assist in the support of manufacturing operations including process validation, environmental monitoring, and utilities as applicable. Perform review and release of stability and release tests for compliance to SOPs and regulatory requirements and ensure data is reported accurately. Prepare lab reports as required. Assist with root cause investigations for quality incidents related to chemical analysis for stability and release tests. Maintain Quality System records and ensure completeness and accuracy. Coordinate with department management to identify and implement compliant process improvements. Clarify regulations, policies, and procedures to internal teams as applicable. Coordinates with departmental leaders to develop appropriate corrective actions resulting from investigations, internal audits, and facility inspections. Conduct follow-up checks on the effectiveness of corrective actions Performs other duties to support Quality Systems and Regulatory Affairs department as assigned. Education: Bachelor's degree in chemistry or related field required. Experience: Five or more years' experience within a pharmaceutical manufacturing (cGMP) laboratory environment. Should have a working knowledge of pharmaceutical manufacturing requirements, Quality System principles (Documentation, Training, Investigations/CAPA, Change Control, etc), and global Quality Control regulations. Should have method development and validation experience. Experience with MasterControl or other electronic quality management system preferred. Skills & Knowledge: Good oral, written, communication, and interpersonal skills. Ability to develop and maintain cooperative working relationships with others. Effectively interfaces with multiple levels of associates within the organization, including management and plant associates. Ability to work independently. Ability to handle a variety of tasks simultaneously. Attention to detail. Familiarity with concepts of electronic documentation management systems (EDMS). Work Environment: The work environment characteristics described here are representative of those an associate may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: General pharmaceutical laboratory, production, and warehouse facility. The noise level in the facility is moderate. Physical & Mental Requirements: The physical demands described here are representative of those that must be met by an associate to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: Physical activity requiring reaching, bending, kneeling, stooping, lifting, finger dexterity, grasping, feeling, repetitive motions, talking and hearing. Ability to lift up to 50 lbs. Visual requirement is for close vision, distance vision, peripheral vision and ability to adjust focus. Associate is required to stand, walk (or otherwise be mobile). Ability to deal with stressful situations as they arise. What Cencora offers We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members' ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more. For details, visit ************************************** Full time Equal Employment Opportunity Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law. The company's continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory. Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call ************ or email ****************. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned Affiliated CompaniesAffiliated Companies: AmerisourceBergen Drug Corporation

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Under the general direction of the Senior Manager of Regulatory Affairs & Stability, the QC/Stability Chemist will focus on stability and release testing, as required, of products repackaged at AHP and work closely with other departments within the Quality Unit to ensure drug product meets all standards. * Ensure stability and release testing activities are compliant with FDA, DEA, other regulatory body requirements as applicable. Ensure compliance with local and corporate policies and procedures. * Perform stability and release testing for drug products in accordance with compendial and global requirements, as applicable. * Develop, revise, and review standard operating procedures (SOPs), work instructions (WIs), and test method documents to ensure compliance with applicable compendia and regulations. * Assist in the support of manufacturing operations including process validation, environmental monitoring, and utilities as applicable. * Perform review and release of stability and release tests for compliance to SOPs and regulatory requirements and ensure data is reported accurately. * Prepare lab reports as required. * Assist with root cause investigations for quality incidents related to chemical analysis for stability and release tests. * Maintain Quality System records and ensure completeness and accuracy. * Coordinate with department management to identify and implement compliant process improvements. * Clarify regulations, policies, and procedures to internal teams as applicable. * Coordinates with departmental leaders to develop appropriate corrective actions resulting from investigations, internal audits, and facility inspections. * Conduct follow-up checks on the effectiveness of corrective actions * Performs other duties to support Quality Systems and Regulatory Affairs department as assigned. Education & Experience: * Bachelor's degree in chemistry or related field required. Three or more years' experience within a pharmaceutical manufacturing (cGMP) laboratory environment. Should have a working knowledge of pharmaceutical manufacturing requirements, Quality System principles (Documentation, Training, Investigations/CAPA, Change Control, etc), and global Quality Control regulations. * Experience with MasterControl or other electronic quality management system preferred. Skills & Knowledge: * Good oral, written, communication, and interpersonal skills. * Ability to develop and maintain cooperative working relationships with others. * Effectively interfaces with multiple levels of associates within the organization, including management and plant associates. * Ability to work independently. * Ability to handle a variety of tasks simultaneously. * Attention to detail. * Familiarity with concepts of electronic documentation management systems (EDMS). Environment: The work environment characteristics described here are representative of those an associate may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: General pharmaceutical laboratory, production, and warehouse facility. The noise level in the facility is moderate. Physical & Mental Requirements: The physical demands described here are representative of those that must be met by an associate to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: * Physical activity requiring reaching, bending, kneeling, stooping, lifting, finger dexterity, grasping, feeling, repetitive motions, talking and hearing. * Ability to lift up to 50 lbs. * Visual requirement is for close vision, distance vision, peripheral vision and ability to adjust focus. * Associate is required to stand, walk (or otherwise be mobile). * Ability to deal with stressful situations as they arise. What Cencora offers We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members' ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more. For details, visit ************************************** Full time Equal Employment Opportunity Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law. The company's continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory. Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call ************ or email ****************. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned Affiliated Companies Affiliated Companies: AmerisourceBergen Drug Corporation

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Under the general direction of the Senior Manager of Regulatory Affairs & Stability, the QC/Stability Chemist will focus on stability and release testing, as required, of products repackaged at AHP and work closely with other departments within the Quality Unit to ensure drug product meets all standards. Ensure stability and release testing activities are compliant with FDA, DEA, other regulatory body requirements as applicable. Ensure compliance with local and corporate policies and procedures. Perform stability and release testing for drug products in accordance with compendial and global requirements, as applicable. Develop, revise, and review standard operating procedures (SOPs), work instructions (WIs), and test method documents to ensure compliance with applicable compendia and regulations. Assist in the support of manufacturing operations including process validation, environmental monitoring, and utilities as applicable. Perform review and release of stability and release tests for compliance to SOPs and regulatory requirements and ensure data is reported accurately. Prepare lab reports as required. Assist with root cause investigations for quality incidents related to chemical analysis for stability and release tests. Maintain Quality System records and ensure completeness and accuracy. Coordinate with department management to identify and implement compliant process improvements. Clarify regulations, policies, and procedures to internal teams as applicable. Coordinates with departmental leaders to develop appropriate corrective actions resulting from investigations, internal audits, and facility inspections. Conduct follow-up checks on the effectiveness of corrective actions Performs other duties to support Quality Systems and Regulatory Affairs department as assigned. Education & Experience: Bachelor's degree in chemistry or related field required. Three or more years' experience within a pharmaceutical manufacturing (cGMP) laboratory environment. Should have a working knowledge of pharmaceutical manufacturing requirements, Quality System principles (Documentation, Training, Investigations/CAPA, Change Control, etc), and global Quality Control regulations. Experience with MasterControl or other electronic quality management system preferred. Skills & Knowledge: Good oral, written, communication, and interpersonal skills. Ability to develop and maintain cooperative working relationships with others. Effectively interfaces with multiple levels of associates within the organization, including management and plant associates. Ability to work independently. Ability to handle a variety of tasks simultaneously. Attention to detail. Familiarity with concepts of electronic documentation management systems (EDMS). Environment: The work environment characteristics described here are representative of those an associate may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: General pharmaceutical laboratory, production, and warehouse facility. The noise level in the facility is moderate. Physical & Mental Requirements: The physical demands described here are representative of those that must be met by an associate to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: Physical activity requiring reaching, bending, kneeling, stooping, lifting, finger dexterity, grasping, feeling, repetitive motions, talking and hearing. Ability to lift up to 50 lbs. Visual requirement is for close vision, distance vision, peripheral vision and ability to adjust focus. Associate is required to stand, walk (or otherwise be mobile). Ability to deal with stressful situations as they arise. What Cencora offers We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members' ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more. For details, visit ************************************** Full time Equal Employment Opportunity Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law. The company's continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory. Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call ************ or email ****************. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned Affiliated CompaniesAffiliated Companies: AmerisourceBergen Drug Corporation

Our Hebron, OH Facility is Looking for a Lab Chemist I, they will be responsible for sample preparation, the analysis of samples to determine their chemical and physical properties. This is a traditional, white lab coat position that offers no travel and a flexible schedule! We are looking for an experienced individual with good work ethic. Pay: $23 Shift: 1st Why work for Clean Harbors? Health and Safety is our #1 priority and we live it 3-6-5! Competitive wages Comprehensive health benefits coverage after 30 days of full-time employment Generous paid time off, company paid training and tuition reimbursement Positive and safe work environments Opportunities for growth and development for all the stages of your career Key Qualifications: High school diploma or equivalent Bachelor's degree in chemistry or physical science is preferred. Ability to work in a team environment. Clean Harbors is the leading provider of environmental, energy and industrial services throughout United States and Canada, as well as Mexico and Puerto Rico. The Company serves a diverse customer base, including a majority of the Fortune 500 companies, thousands of smaller private entities and numerous federal, state, provincial and local governmental agencies. Through its Safety-Kleen subsidiary, Clean Harbors also is a premier provider of used oil recycling and re-refining, parts washers and environmental services for the small quantity generator market. For many positions, we have implemented a Competency Based Progression and Pay Program, which directly rewards employees for developing increased proficiency in their key job functions through training and experience. At Clean Harbors you are offered unique opportunities for all stages of your career. To learn more about our company visit us at ********************* We thank all those interested in joining the Clean Harbors team; however only those that complete the online application and meet the minimum job qualifications will be considered for this role. -CS- Key Responsibilities: Ensures Health and Safety is the number one goal by following policies, processes, and acting in a safe manner at all times. Responsible for maintaining a safe working environment that is in compliance with all applicable OSHA regulations as well as all applicable company Health and Safety and Compliance protocols. Performs analysis of samples following prescribed procedures, with the ability to solve minor problems. Calibrates and utilizes instrumentation. Maintenance of equipment and suggests solutions to problems. Completes all paperwork associated with the analyses in a neat and timely fashion. Ensures that all work meets applicable QA/QC guidelines. Responsibility for supply management in their area of responsibility, including proper housekeeping and best management practices. Responsible for proper management of waste generated as a result of analytical procedures.

Are you passionate about significantly improving the future of medicine? Do you believe that people are the most important asset of any company? If so, join AmplifyBio! AmplifyBio is a leading contract research organization with a comprehensive range of services that span from being an outsourcing partner for discovery stage R&D work, a preclinical CRO performing safety efficacy and toxicology studies for small molecules and advanced therapies alike, and, most recently, an expansion into manufacturing services for cell, gene, and mRNA-based therapeutics. The AmplifyBio ecosystem is comprised of three distinct business units: ADOC (South San Francisco, CA)- Amplify's Discovery, Optimization, and Characterization laboratories: ASET (West Jefferson, OH) - Amplify's Safety, Efficacy, and Toxicology Site; and the most recently opened AMEC (New Albany, OH) - Amplify's Manufacturing Enablement Center. About ASET West Jefferson, OH: AmplifyBio's safety, efficacy, and toxicology unit (ASET) was launched as a preclinical CRO that spun out of Battelle in 2021 to address the changing needs of commercial organizations developing modern therapeutics. AmplifyBio brings decades of experience to accommodate a wide variety of GLP and non-GLP studies in all in vivo models and dose routes. Among the investments that AmplifyBio has made to empower preclinical assessments of advanced therapies is building a new state-of-the-art analytical laboratory to include molecular and immunological assays that assess critical safety and efficacy indicators for cell and gene therapies during preclinical studies AmplifyBio is currently seeking to hire an Assistant/Associate Scientist to join our growing Analytical Sciences team ! The Assistant/Associate Scientist is responsible for performing analytical testing using a variety of cellular and/or molecular biology analysis platforms. Level of position and title will be based on experience and will report to a supervisor or senior scientist of Analytical Sciences . What You'll Do Here: Perform work in a laboratory setting using a variety of cellular and/or molecular biology analysis platforms. Collect and review data using manual and/or electronic systems. Develop and maintain a good working knowledge of laboratory equipment and experimental procedures to perform assigned laboratory tasks. Communicates routine updates (including technical challenges) on assigned tasks. Recognizes deviations and unusual occurrences notifying responsible individuals promptly and contributes to corrective actions. Complete and maintain training to remain compliant with all regulatory and health/safety requirements. Train less experienced staff as needed. Assists other departments as needed. We Would Love to Hear from You If: Bachelor's degree in molecular biology, Biochemistry, Immunology, Molecular Genetics, or related field. A minimum of 1 year of related work experience in performing cell or molecular assay techniques (e.g., qPCR, dPCR, cytokine analysis, ELISA, PBMC isolation, flow cytometry). Excellent documentation, organization, communication (oral and written), multi-tasking and problem-solving skills. Ability to work independently and in a collaborative team environment. Ability to follow all appropriate regulatory requirements to ensure experimental data are accurately recorded and verified. Ability to work in a BSL-2 research laboratory environment which includes periods of bench-work, working in a bio-safety cabinet, and ability to wear respiratory protection. Must be willing to be immunized with licensed and FDA approved vaccines and medications recommended for persons at risk to occupational exposures. Must have the flexible schedule to accommodate non-standard work hours. Must be able to work more than 40 hours a week (including weekend and holidays) when needed to accomplish necessary tasks. Knowledge of Food and Drug Administration's (FDA) Good Laboratory Practice (GLP) Regulations, 21 CFR Part 58 for the conduct of nonclinical laboratory studies. At AmplifyBio, we're committed to growing and empowering an inclusive community within our company and industry. This is why we hire and cultivate diverse teams of the best and brightest from all backgrounds, experiences, and perspectives across our organization. AmplifyBio is an equal opportunity employer, and we value diversity at our company. We don't discriminate on the basis of race, color, citizenship status, national origin, ancestry, gender (including gender expression and gender identity), sexual orientation, age, weight, religion, creed, physical or mental disability, marital status, veteran status, political affiliation, or any other factor protected by federal, state, or local law. Why You Will Love Working Here: We take the health and happiness of our employees seriously and consistently evaluate new ways to Amp up our benefits to provide an amazing place to work. From a wellness program (did we mention we have an onsite gym with state-of-the-art equipment and ping pong table?), to financial planning and legal assistance, we make sure to take care of our own. Health, Dental, and Vision insurance that starts on your first day at AmplifyBio! Competitive Compensation Package We take work-life balance seriously and we back it up with a FLEXIBLE PTO policy! Generous paid parental leave Wellness and Self-Care Programs 401(k) match Tuition Reimbursement EAP/work-life support system A fun work environment where everyone's voice matters! We are just getting started! More benefits on the way! An Opportunity to Change the World!!! When you join our team, you will be a part of groundbreaking work while collaborating with our clients, research scientists, study directors, lab technicians, and specialists across a variety of disciplines. The future for AmplifyBio is as great as the combination of our imaginations and actions, and we hold ourselves accountable for our choices and results. We have a bias for action, excellence, and, especially, the health and safety of our employees.

To perform routine, workflow processes within the quality control laboratory to meet customer requirements by supporting the testing of raw materials and finished products while ensuring regulatory compliance standards and release times are met. Responsibilities Perform qualitative, quantitative chemical and physical testing and as specified by compendia or specification for raw materials, packaging components and finished products and intermediates Maintain laboratory data in an orderly manner in laboratory notebooks, worksheets and documents Perform peer review of analytical testing documentation Perform peer review of analytical testing documentation. Complete and/or conduct required training according to the laboratory and site curriculum. Other Duties as assigned Qualifications BS in Chemistry or a science-related field. One or more years of pharmaceutical experience preferred. Required: hands-on experience with the following, preferably in a GMP or industrial setting: pH meters Analytical Balances and scales Computer applications (Microsoft Office - Excel, Word, PowerPoint) Basic statistical inference (standard deviation, linear regression tools) Required: ability to work independently using a team approach to accomplish tasks assigned; ability to work on multiple projects in a fast pace environment. Required: good written and verbal communication skills. Prior work related experiences or knowledge that are highly desirable include: Validation, execution and transfer of analytical methods Compendial testing of raw materials (APIs, excipients, package components) Pharmaceutical products and intermediate testing. The individual must be able to perform compendial and non-compendial testing for multiple projects at one time. Experience with Empower data analysis software. cGMP, DEA, or other regulated environment Hands-on experience with the following analytical techniques is highly desirable, in a scholastic or industrial setting. Individual will receive formal training in these techniques as appropriate to their specific role: Chromatography: HPLC, GC, IC, uPLC Spectroscopy: UV, UV/Vis, IR/FTIR, Raman, NIR, XRF, IonScan Dissolution Physical Tests: Particle Sizing, microscopy, DSC, TGA, XRD Specialized pharmaceutical testing (Compendial Monograph or General Chapter, dissolution) Working knowledge of the specified equipment and techniques to perform troubleshooting is highly desired. What We Offer Clean climate-controlled working environment (Operator roles at the top) Annual performance bonus potential 401k employer match up to 6% of your contributions 23 vacation/personal days 11 paid Company holidays Generous healthcare benefits Employee discount program Wellbeing rewards programs Safety and Quality is a top organizational priority Career advancement/growth opportunities Tuition Reimbursement Maternity and Parental Leave *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 a specific plan or program terms.

Transcendia is a leader in custom engineered materials for critical product components in a wide range of markets and applications. The company provides deep material science expertise, outstanding customer service through broad geographic coverage and trusted product reliability. Job Summary: Provides support to R&D activities by conducting a wide range of physical and chemical testing on materials, assisting with product development activities, and providing support for product regulatory management. Job Duties: Performs research activities in a a laboratory environment to aid in the planning, designing, and conducting of experiments. Conducts routine maintenance and safety checks on lab equipment to ensure working order Collects, prepares, and tests samples and records measurements or observations. Conducts specialized tests and evaluations of materials and packaging samples in support of departmental activities including, but not limited to the following: Tensile tests (seal strength, elongation, tensile strength, yield strength) Material chemical characterization (FTIR) Optical Microscopy skills Tear resistance, impact/puncture strength Heat seal and other package strength characterizations May be responsible for cleaning, disinfecting, and maintaining cleanrooms and equipment. Provides support as needed for plant and pilot line trials Works with Supply Chain function and suppliers to maintain product regulatory data Maintains confidentiality on development projects, tests, products, and equipment Prepares test reports and maintains files and records Other duties as assigned Job Qualifications: High school diploma or general education degree (GED), plus two to four years of related experience and/or training; technical/science Associates, Bachelor's degree or technical school preferred Up to three years experience in a manufacturing setting, Manufacturing Lab Tech experience preferred Proficient in Excel and Word Must have organizational skills with an ability to prioritize and multi-task Must possess good problem-solving skills Ability to interact in a professional manner with employees and vendors Ability to communicate effectively both verbally and in writing Must be dedicated to continuous improvement Willingness to work as team member or independently Transcendia is an equal opportunity employer and will consider all candidates for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

We are seeking a dedicated QC Scientist I to join our team. This role involves bench testing, including sample preparation, wet chemistry, standard weighing, and dilutions. Over time, you will receive training on HPLC and GC and work in both the Oral Dose Solids and Nasals departments. You will conduct chemical and physical analyses to support the development of manufacturable multisource pharmaceutical products. Additionally, you will provide analytical support for the release of registration materials for regulatory submissions and assist in analytical method validation and transfer activities. Responsibilities * Perform assigned analytical tasks in support of product development, registration lot release, and regulatory submission activities. * Conduct activities within assigned timelines and in compliance with cGXP's and company practices and procedures. * Follow work instructions, SOPs, and company practices. * Document analytical activities and results accurately, timely, and right-first-time to maintain data integrity. * Follow written analytical procedures and identify execution challenges of analytical methods. * Support troubleshooting activities. Essential Skills * Proficiency in sample preparation, dilutions, and wet chemistry. * Experience in quality control and chemical testing. * Bachelor's degree in a science field. * Strong chemistry lab experience, which may include academic experience. * Ability to work in a fast-paced environment and handle multiple tasks. * Excellent written and verbal communication skills. * Ability to work with supervision using scientific judgment and professional competency. Additional Skills & Qualifications * Bachelor's degree in Chemistry or Biochemistry preferred. * Experience in a lab setting outside of academia is strongly preferred. * Experience in Biology, Microbiology, or Pharmaceutical Science with strong chemistry lab experience will be considered. * Ability to work effectively in a team environment. Work Environment This is a fast-paced environment where you will work in both the quality group and occasionally the manufacturing area. The position is for the 2nd shift, Monday to Friday, from 2 PM to 10:30 PM, with some flexibility. Initially, you will work five 8-hour shifts, with the potential to switch to four 10-hour shifts after training. Pay and Benefits The pay range for this position is $24.00 - $24.00/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 Columbus,OH. Application Deadline This position is anticipated to close on Apr 18, 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.

Transcendia is a leader in custom engineered materials for critical product components in a wide range of markets and applications. The company provides deep material science expertise, outstanding customer service through broad geographic coverage and trusted product reliability. Job Summary: Provides support to R&D activities by conducting a wide range of physical and chemical testing on materials, assisting with product development activities, and providing support for product regulatory management. Job Duties: * Performs research activities in a a laboratory environment to aid in the planning, designing, and conducting of experiments. * Conducts routine maintenance and safety checks on lab equipment to ensure working order * Collects, prepares, and tests samples and records measurements or observations. * Conducts specialized tests and evaluations of materials and packaging samples in support of departmental activities including, but not limited to the following: * Tensile tests (seal strength, elongation, tensile strength, yield strength) * Material chemical characterization (FTIR) * Optical Microscopy skills * Tear resistance, impact/puncture strength * Heat seal and other package strength characterizations * May be responsible for cleaning, disinfecting, and maintaining cleanrooms and equipment. * Provides support as needed for plant and pilot line trials * Works with Supply Chain function and suppliers to maintain product regulatory data * Maintains confidentiality on development projects, tests, products, and equipment * Prepares test reports and maintains files and records * Other duties as assigned Job Qualifications: * High school diploma or general education degree (GED), plus two to four years of related experience and/or training; technical/science Associates, Bachelor's degree or technical school preferred * Up to three years experience in a manufacturing setting, * Manufacturing Lab Tech experience preferred * Proficient in Excel and Word * Must have organizational skills with an ability to prioritize and multi-task * Must possess good problem-solving skills * Ability to interact in a professional manner with employees and vendors * Ability to communicate effectively both verbally and in writing * Must be dedicated to continuous improvement * Willingness to work as team member or independently Transcendia is an equal opportunity employer and will consider all candidates for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.