GMP Associate Chemist -Reference Standards at Eurofins

Foster City, California, United States -

Full Time

Start Date

Immediate

Expiry Date

15 Oct, 26

Salary

70000.0

Posted On

17 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Chemistry, GMP Compliance, HPLC, UPLC, FTIR, NMR, TGA, DSC, Karl Fischer Titration, Empower Software, Technical Writing, Data Analysis, Project Management, SOP Adherence, Method Troubleshooting, Laboratory Documentation

Industry

Medical and Diagnostic Laboratories

Description

Company 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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Job Description Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for a GMP Chemist in our Professional Scientific Services group in Foster City, CA. QC Chemist Responsibilities: Support the qualification and requalification of Reference Standards through analytical testing techniques such as Appearance testing, FTIR, NMR, Liquid Chromatography (LC/HPLC/UPLC), TGA, DSC, and Karl Fischer titration, including performing correction factor calculations. Ensure adherence to GMP regulations by completing required training, following Standard Operating Procedures (SOPs), and maintaining compliance-related documentation. Review and verify laboratory documentation, calculations, and test preparations before sample analysis to help prevent deviations and laboratory investigations. Perform data analysis and troubleshoot methods and instrumentation. Prepare data for presentations and assist in generating technical reports Coordinate sample shipments and testing activities with external contract laboratories, and accurately document and upload analytical results into internal databases. Work closely with cross-functional teams and external vendors, contract laboratories, and partners to support operational goals. Initiate and perform investigations, as needed Write protocols and technical reports and transfer methods internally and externally Contribute to a safe, organized, and compliant laboratory environment by participating in routine housekeeping and weekly laboratory cleanup activities. Qualifications The Ideal Candidate would possess: Demonstrated success in executing small molecule analytical chemistry methods adhering to SOPs and GMP guidelines. At least 1 year of continuous experience in GMP/ GLP regulated environment. Previous experience conducting and analyzing data for analytical methods such as UPLC/HPLC, FTIR, NMR, Thermogravimetric DSC/TGA, and KF titrations. Understanding of experimentation and data analysis using Empower software (Version III) Excellent written and verbal communication skills and experience interacting with people from a wide range of skill levels and experience Ability to communicate complex scientific findings and recommendations in one-on-one discussions and departmental meetings Excellent technical writing experience such as protocols, reports, and SOPs Demonstrated ability to work as an independent, self-motivated, detail-oriented, result-driven and highly flexible team-player in a fast-paced working environment Strong computer, scientific, and organizational skills Demonstrated exceptional attention to detail and strong project management capabilities, effectively managing project resources, including materials, personnel, and timelines, while proactively identifying and escalating critical issues to project leadership and management. Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Qualifications B.S. in Chemistry or related scientific field and minimum of 2-5 years of experience in an analytical environment, or M.S. degree and 1-3 years of experience Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Compensation Range: $60,000 - $70,000 Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries. We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer. Compensation: USD 55000 - USD 70000 - yearly

Responsibilities

The role involves qualifying reference standards using various analytical techniques and ensuring strict adherence to GMP regulations and SOPs. Responsibilities include performing data analysis, writing technical reports, and coordinating with external contract laboratories.