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Five (5) years of basic chemistry techniques (can be academic) is a plus. The Lead, QC Chemist performs specific routine analysis of samples of raw materials, in process, and finished products according to established test procedures. The Chemist prepares reagents, standards, and solutions and may m

Experience: Bachelor's: Minimum of 6 years or Master's: Minimum of 4 years of experience in a raw material, chemistry, or quality control role, preferably in pharmaceuticals, manufacturing, cosmetics. As a Raw Material Chemist, you will play a critical role in the testing, evaluation, and quality co

Education & Qualification: BS in Chemistry or related scientific disciplines. One (1) year of basic chemistry techniques (can be academic) is a plus. The Chemist, QC 3 performs specific routine analysis of samples of raw materials, in process, and finished products according to established test proc

As a Raw Material Chemist, you will play a critical role in the testing, evaluation, and quality control of raw material samples. Education: Bachelor’s / Master’s degree in Chemistry or other science related field. Experience: Bachelor’s: Minimum of 6 years or Master’s: Minimum of 4 years of

The Chemist, QC 3 performs specific routine analysis of samples of raw materials, in process, and finished products according to established (official and/or in-house) test procedures. The Chemist prepares reagents, standards, and solutions and may monitor and verify quality in accordance with stati

Manager, Quality Control Laboratory. The Chemist prepares reagents, standards, and solutions and may monitor and verify quality in accordance with statistical process and other control procedures.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. 2025, Eurofins generated total revenues of EUR € 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description We are seeking an experienced and highly motivated Raw Material Chemist to join our team. As a Raw Material Chemist, you will play a critical role in the testing, evaluation, and quality control of raw material samples. Your expertise will drive product innovation, quality assurance, and cost-effectiveness while ensuring compliance with industry regulations. Key Responsibilities: • Conduct detailed chemical and physical analyses of raw materials using techniques such as the following, including but not limited to:, • Spectroscopy (FTIR, UV-Vis), • Chromatography (HPLC, GC, TLC), • Dissolution, • Potentiometric Titrations / Assay, • Viscosity, • pH, • Conductivity, • Karl Fisher, • Specific Gravity, • Loss on Drying, • Residue on Ignition, • Oversee the quality control of incoming raw materials and ensure their compliance with company standards. Troubleshoot any material-related issues., • Proven ability to analyze raw material issues, identify root causes, and implement effective solutions., • Strong experience with HPLC and GC testing/techniques and Empower software, • Ability to troubleshoot instrument / equipment issues, • Perform method verifications / validations on new methods, • Perform calibration of instrument / equipment, • Maintain meticulous, accurate and precise records of specifications, test methods, testing data, results, and any deviations from standard procedures., • Evaluate test results for accuracy, • Review / Release raw data, documentation and results for Certificate of Analysis, • Prepare detailed reports for management and regulatory purposes., • Author / revise technical documents including but not limited to specifications, test methods, method verification / validation / transfer protocol or reports, SOPs, investigations, etc., • Ensure that all raw materials comply with industry regulations and safety standards, • Knowledge of current GMP, FDA regulations, ICH guidelines, ISO 17025 and other regulatory requirements as applicable., • Working knowledge of computer skills., • Strong attention to detail, ensuring accurate and precise testing and documentation., • Excellent written and verbal communication skills to effectively report findings and collaborate with cross-functional teams., • Ability to maintain a safe, clean, and orderly laboratory environment., • Ability to work independently and as part of a team, with minimal supervisionQualifications, • Education: Bachelor’s / Master’s degree in Chemistry or other science related field, • Experience: Bachelor’s: Minimum of 6 years or Master’s: Minimum of 4 years of experience in a raw material, chemistry, or quality control role, preferably in pharmaceuticals, manufacturing, cosmetics, • Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Positions are full-time, working Monday-Friday 8am-5pm, overtime as needed. Candidates currently living within commutable distance to North Brunswick, NJ are encouraged to apply. • Comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match

Job Description Date 06/2020 Location 1200 Airport Road, North Brunswick NJ Title Chemist, Quality Control 3 Department Quality Control Reports to Manager, Chemistry Laboratory FLSA (Exempt or Non-Exempt Exempt Role Overview The Chemist, QC 3 performs specific routine analysis of samples of raw materials, in process, and finished products according to established (official and/or in-house) test procedures. Testing assesses the strength, identify, purity of the test samples and/or raw materials. The Chemist prepares reagents, standards, and solutions and may monitor and verify quality in accordance with statistical process and other control procedures. The Chemist maintains organization and compliance while working in a fast-paced environment with changing priorities. The duties and responsibilities described for each level are not limited to those outlined and are not intended to be a comprehensive list of all activities, functions, or responsibilities required of the position. Management reserves the right to modify, assign, or reassign duties and responsibilities at any time based on business needs. Areas of Responsibility • Troubleshoot /test specific batches in order to assist in determining the root cause of off-spec product and makes recommendations for ingredient adjustments to meet required specifications., • Ensures compliance with company and customer specifications as well as federal, state and local regulatory requirements, • Investigates customer complaints and provides management with test results information., • Performs assigned sampling, physical, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished, and stability products in an FDA regulated lab environment. Uses a variety of wet chemicals, physical and instrumental techniques as well as routine QC instruments (HPLC, GC, IR, Auto Titrator, Bulk Density, UV Spectrophotometer, Dissolution, Karl Fisher (KF), Potentiometer)., • Performs complicated testing with supervisory direction. Documents work clearly and performs tests accurately., • Preparation and review of QC related documents is 5%of daily activities., • Test of samples/raws as assigned and reports the results. Testing activities represents 95% of daily work., • Prepares and/or Reviews Test Procedures, SOP's and Protocols as assigned., • Performs maintenance and calibrations of laboratory instruments /equipment with supervisory direction/training., • Complies with all regulatory/ in-house requirements (may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP,GLP, documentation) when performing the assigned activity., • Must be able to work extended hours as needed and occasional weekends., • Works in a safe and responsible manner to create an injury-free and incident-free workplace., • Complies with all job-related safety and other training requirements. Education & Qualification: • BS in Chemistry or related scientific disciplines, • One (1) year of basic chemistry techniques (can be academic) is a plus, • Ability to maintain integrity and honesty at all times and to communicate with transparency., • Ability to work independently or as part of a team., • Solid understanding of cGMP’s and GLP and is familiar with 21 CFR Part 11, • Strong working knowledge of Microsoft Word, Excel., • Good documentation practices and able to write simple, clear reports, • Meets commitments on time and practices time-management skills, • Seeks to identify continuous improvement needs, • May execute 90%-100% of their work at the bench level either standing or sitting on a stool., • Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from the waist, or squatting, walking short distances and leaning over equipment as well as kneeling on the floor to clean under the equipment., • Must be able to wear all PPE including a lab coat, face mask, booties, gloves, safety glasses/goggles, and respirators., • On occasion may need to lift up to 35 lbs., • Approximately 80% of work performed in a laboratory environment which may have unpleasant odors or hazardous conditions. USPL is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status, or any other characteristic protected by applicable local, state, or federal law. Benefits And Compensation: Our benefits are designed to help you move forward in your career, and in areas of your life outside of USPL. From health and wellness benefit options including: medical, dental, vision, short and long term disability, basic life insurance, supplemental life insurance, AD&D insurance. We also offer a matched 401(k) savings plan. Employees have the opportunity to receive compensation in the form of premium pay such as overtime, shift differential, holiday pay, sick time, etc. Newly hired employees receive up to 10 days of vacation the first year, which grows to 12 days starting the second year of employment. Job Description Acknowledgement I have read and understand the job requirements, responsibilities, and expectations set forth in the job description provided for my position. I attest that I can perform the essential job functions as outlined with or without any reasonable accommodations.

Job Description Join a high-impact team at the forefront of environmental response and analytical science. CSS is seeking a skilled Environmental Analytical Chemist to support critical field and laboratory operations, delivering real-time data that informs decisions during environmental and national response efforts. Our mobile laboratories play a critical role in supporting Incidents of National Significance. This team provides rapid, on-site and remote chemical analysis to detect toxic industrial chemicals, chemical warfare agents, and their degradation products across diverse environmental matrices (air, soil, water, and surface wipe). Your work will directly contribute to public safety, environmental protection, and national response readiness. Key Responsibilities: • Perform quantitative and qualitative analysis of environmental samples to determine physical and chemical properties using advanced analytical techniques in organic and physical chemistry, • Operate and maintain sophisticated instrumentation, including Gas Chromatography/Mass Spectrometry (GC/MS) and Electron Capture Detection (ECD) systems within mobile laboratory environments, • Execute a wide range of EPA analytical methods, including SW-846 methods 8260, 8270, 8081, 8082, and others, • Conduct sample receipt, logging, and preparation for laboratory analysis while ensuring strict adherence to quality control protocols, • Maintain, calibrate, and troubleshoot laboratory instrumentation; manage laboratory supplies and inventory, • Collaborate with chemists and cross-functional teams to support analytical workflows and problem-solving efforts, • Participate in planning and strategy discussions; recommend improvements to protocols, standard operating procedures (SOPs), instrumentation, and analytical techniques, • U.S. Citizenship is required, • Minimum of 3+ years of hands-on experience in environmental organic analytical laboratory operations, • Demonstrated experience working with Agilent instrumentation, including GC/MS systems, • Bachelor's degree in Chemistry or a related physical science, • Strong understanding of organic sample preparation and chromatographic techniques, • Ability to start within 2–3 weeks and work on-site in Edison, NJ, • Willingness and ability to travel as needed, including deployment to field locations in support of environmental emergency response operations, • Ability to successfully pass and maintain a National Agency Check (NACI) background investigation and complete a pre-employment drug screening, • Experience with Agilent MSD MassHunter software, • Experience with Laboratory Information Management Systems (LIMS), • Familiarity with EPA methods for organic chemistry analysis, • OSHA HAZWOPER certificationCSS is an Equal Opportunity/Affirmative Action Employer who provides equal employment opportunities to all employees and applicants for employment without regards to race, color, religion, sex, gender identity, sexual orientation, pregnancy, national origin, age, disability, veteran status or genetic information. In addition to federal law requirements, CSS complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Job Description Job Description Date 02/2024 Location 1300 Airport Road, North Brunswick NJ Title Lead, Quality Control Chemist Department Quality Control Reports to Manager, Quality Control Laboratory FLSA (Exempt or Non-Exempt Exempt Role Overview The Lead, QC Chemist performs specific routine analysis of samples of raw materials, in process, and finished products according to established (official and/or in-house) test procedures. Testing assesses the strength, identify, purity of the test samples and/or raw materials. The Chemist prepares reagents, standards, and solutions and may monitor and verify quality in accordance with statistical process and other control procedures. The Chemist maintains & organizes testing’s and compliance while working in a fast-paced environment with changing priorities. The duties and responsibilities described for each level are not limited to those outlined and are not intended to be a comprehensive list of all activities, functions, or responsibilities required of the position. Management reserves the right to modify, assign, or reassign duties and responsibilities at any time based on business needs. Areas of Responsibility • Performs assigned sampling, physical, chemical tests and assay on raw materials, active dietary ingredients, in-process, finished, and stability products in an FDA regulated lab environment. Uses a variety of wet chemicals, physical and instrumental techniques as well as routine QC instruments HPLC, GC, IR, Auto Titrator, Bulk Density, UV Spectrophotometer, Dissolution, Karl Fisher (KF), Potentiometer., • Troubleshoots HPLC, GC, QC instruments for specific tests in order to assist in determining the root cause of aberrant results and help in performing Lab investigations / OOS., • Evaluates daily raw data sheets for product samples and release, if needed., • Coordinates annual review of STPS / SOPS as per USPL procedures., • Prepare new methods and test procedures for new or existing raw materials and finished products., • Ensures compliance with company and customer specifications as well as federal, state and local regulatory requirements., • Perform floor supervision of QC Chemists for routine testing, if required., • Prepares and reviews QC related documents during and finishing of testing of sample. Submit all testing related documents like data sheets, chromatograms, spectras, instruments print outs in timely manner to Qc Documentation department to release the batch of raw material / finished product., • Prepares and/or Reviews Test Procedures, SOP's and Protocols as assigned., • Performs maintenance and calibrations of laboratory instruments /equipment, if required to help in-house calibrations., • Assures GMP compliance according to FDA CFR Part 111 and USPL SOPs / guidelines., • Complies with all regulatory/ in-house requirements (may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP, GLP, documentation) when performing the assigned activity., • Trains new QC Chemists to perform instrumental testing., • Must be able to work extended hours as needed and occasional weekends., • Works in a safe and responsible manner to create an injury-free and incident-free workplace., • Complies with all job-related safety and other training requirements. Education & Qualification: • BS/MS in Chemistry or related scientific disciplines., • Five (5) years of basic chemistry techniques (can be academic) is a plus., • Ability to maintain integrity and honesty at all times and to communicate with transparency., • Ability to work independently or as part of a team., • Solid understanding of cGMP’s and GLP and is familiar with 21 CFR Part 11., • Strong working knowledge of Microsoft Word, Excel., • Good documentation practices and able to write simple, clear reports., • Meets commitments on time and practices time-management skills., • Seeks to identify continuous improvement needs., • Experience with Shimadzu LC2010, Nexera, GC2010, Thermo ICP-MS, Labsolution and Waters, • Empower Lab Software a plus. Physical Requirements (lifting, etc.): • Ability to navigate office, lab, and/or plant floor working environments., • Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from the waist, or squatting, walking short distances and leaning over equipment as well as kneeling on the floor to clean under the equipment., • Must be able to wear all PPE including a lab coat, face mask, booties, gloves, safety glasses/goggles, and respirators., • Work is regularly performed inside a laboratory environment where temperatures can be moderate, exposure to dust, odors, noise, and fumes. The noise level is usually moderate. Employees can be exposed daily to chemicals and cleaning agents., • May execute up to 20% of their work at the bench level either standing or sitting on a stool. USPL is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status, or any other characteristic protected by applicable local, state, or federal law. Benefits And Compensation: Our benefits are designed to help you move forward in your career, and in areas of your life outside of USPL. From health and wellness benefit options including: medical, dental, vision, short and long term disability, basic life insurance, supplemental life insurance, AD&D insurance. We also offer a matched 401(k) savings plan. Employees have the opportunity to receive compensation in the form of premium pay such as overtime, shift differential, holiday pay, sick time, etc. Newly hired employees receive up to 10 days of vacation the first year, which grows to 12 days starting the second year of employment. Job Description Acknowledgement I have read and understand the job requirements, responsibilities, and expectations set forth in the job description provided for my position. I attest that I can perform the essential job functions as outlined with or without any reasonable accommodation.

Bachelor's Degree in Chemistry or related scientific field and 3+ years' industry experience as a Chemist or Master's Degree in Chemistry or related scientific field and 1+ years' industry experience as a Chemist. The Quality Control Chemist for the drug product testing reports to the Finished Produ

We are seeking an experienced Manufacturing Process Engineer with experience in powder-based manufacturing, with a strong chemistry background to lead and optimize manufacturing operations. This role is responsible for the design, improvement, and oversight of production processes, ensuring efficien

This Chemist II will run Chemistry analytical testing and conduct method development in a GMP team environment. A pharmaceutical testing lab in South Plainfield, NJ is growing their team with an experienced Chemistry Analyst. Conduct GMP analytical testing and wet chemistry analysis including HPLC,

The Analytical Lab primarily serves as a quality control lab for manufacturing that is responsible for routine testing of monomer mixtures and incoming raw materials, releasing raw materials, and ensuring overall compliance to the quality system. Maintain data records, logbooks, forms, audits, vendo

The Analytical Lab primarily serves as a quality control lab for manufacturing that is responsible for routine testing of monomer mixtures and incoming raw materials, releasing raw materials, and ensuring overall compliance to the quality system. Proven wet chemistry skills are a must. Maintain data

Mauser Packaging Solutions - - Responsibilities: Perform all inspection functions as described in applicable Standard Operating Procedures; Inspect all parts and find all defects and report them; Visual inspection of products from raw materials, molding, assembly and shipping; Help ensure rework is

This Chemist II will run Chemistry analytical testing and conduct method development in a GMP team environment. A pharmaceutical testing lab in South Plainfield, NJ is growing their team with an experienced Chemistry Analyst. Conduct GMP analytical testing and wet chemistry analysis including HPLC,

The Analytical Lab primarily serves as a quality control lab for manufacturing that is responsible for routine testing of monomer mixtures and incoming raw materials, releasing raw materials, and ensuring overall compliance to the quality system. Proven wet chemistry skills are a must. Maintain data

Here’s the deal—The client is looking for a hands-on Process Engineer to optimize operations, improve efficiency, and drive continuous improvement across manufacturing processes.Analyze and improve production workflows to boost performance and reduce waste.Partner cross-functionally with enginee

In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change.We bring a human touch to every treatment we pioneer.The primary purpose of

Prepare microbiological media, perform QC sterility checks, and media growth promotion testing.Aseptically prepare and weigh specimens, maintain a clean workspace.Conduct microbiological testing of water samples following standard procedures.Maintain accurate, up-to-date laboratory records.Perform g

This high-impact group ensures the continued quality of our generic and specialty pharmaceutical products. Execute foundational Wet Chemistry techniques, including pH, viscosity, and titrations.

Conduct sample receipt, logging, and preparation for laboratory analysis while ensuring strict adherence to quality control protocols. CSS is seeking a skilled Environmental Analytical Chemist to support critical field and laboratory operations, delivering real-time data that informs decisions durin

High school diploma or equivalent; a technical degree in quality control, engineering, or a related field is preferred. The Quality Inspector for metal stamping plays a crucial role in ensuring that all products manufactured meet specified quality standards and customer expectations throughout the p

Join Our Team as a Website Tester at Little Wheel.Little Wheel is a gambling technology company focused on researching and building products that put players first.We are currently hiring Website Testers across Michigan, New Jersey, Pennsylvania, and West Virginia.This is a great opportunity to earn

Lead the quality review and timely submission of all OTC drug and cosmetic MedWatch reports to the FDA, managing correspondence with partner companies and vendors. Notify relevant partner contacts and manufacturing sites of potential quality-related complaints.

Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.

Join Our Team as a Website Tester at Little Wheel Little Wheel is a gambling technology company focused on researching and building products that put players first.We are currently hiring Website Testers across Michigan, New Jersey, Pennsylvania, and West Virginia.This is a great opportunity to earn

Lead the quality review and timely submission of all OTC drug and cosmetic MedWatch reports to the FDA, managing correspondence with partner companies and vendors. Notify relevant partner contacts and manufacturing sites of potential quality-related complaints.

Prepare and present quality performance reports to management, including analysis of quality metrics and any corrective actions taken. High school diploma or equivalent; a technical degree in quality control, engineering, or a related field is preferred. The Quality Inspector for metal stamping play

Additional infection control and safety policies may apply.

JP is open and accepting candidates with strong mechanical ability.I don't consider analytical, biology, or pharmaceutical background.Some have master or PhD degree, which is over qualified for this contractor position.Some is fresh graduate which doesn't have much hands-on skills.Client refinery ca

We are inspired by a single vision – transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meanin

Follow all safety, quality, and compliance requirements while working in controlled and cleanroom environments.

Ensures all instruments have been properly calibrated, maintenance procedures performed and scheduled quality control completed and documented prior to analysis of patient samples,. Quality Control is performed and documented as scheduled in the same manner as patient samples, resolving all QC failu

Follow all safety, quality, and compliance requirements while working in controlled and cleanroom environments. Eurofins partners with global leaders to help ensure product safety, quality, and regulatory compliance.

Assumes responsibility for procedural and systems controls.

Work Schedule: Mon - Fri, Business Hours.Worker's location based out of the Warren, NJ site and will work both Warren sites as needed.At Client, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one

Follow all safety, quality, and compliance requirements while working in controlled and cleanroom environments. Eurofins partners with global leaders to help ensure product safety, quality, and regulatory compliance.

Additional infection control and safety policies may apply.

The Analytical Lab primarily serves as a quality control lab for manufacturing that is responsible for routine testing of monomer mixtures and incoming raw materials, releasing raw materials, and ensuring overall compliance to the quality system. Proven wet chemistry skills are a must. Maintain data

This role is 100% ONSITE Work Schedule: Mon - Fri, Business Hours Worker's location based out of the Warren, NJ site and will work both Warren sites as needed At Client, we are inspired by a single vision – transforming patients' lives through science.In oncology, hematology, immunology and cardio

This Chemist II will run Chemistry analytical testing and conduct method development in a GMP team environment. A pharmaceutical testing lab in South Plainfield, NJ is growing their team with an experienced Chemistry Analyst. Conduct GMP analytical testing and wet chemistry analysis including HPLC,