Eurofins PSS Insourcing Solutions
Pharma Lab Scientist – GMP & Mass Spec
Eurofins PSS Insourcing Solutions, New York, New York, us, 10261
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.
Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
If you’re looking for a rewarding career, apply with us today!
Job Description Make an Impact in Pharmaceutical Safety: Join Eurofins, a global leader in analytical testing, and help ensure the safety and integrity of pharmaceutical products. As part of our team, you’ll use advanced instrumentation to detect and analyze extractables and leachables; substances that could migrate from packaging or manufacturing components into drug products.
Responsibilities
Perform testing using GC-MS, LC-MS, and/or ICP-MS in a GMP-regulated lab
Analyze and interpret complex data to support clinical and commercial studies
Author technical summaries and contribute to method validation
Troubleshoot instrumentation and lab techniques
Maintain compliance with cGxP standards and regulatory requirements
Collaborate with peers and vendors in a professional lab environment
Qualifications
Bachelor’s degree in chemistry or related field with 2+ years of industry experience, or a Master’s degree with relevant experience
Hands‑on experience with mass spectrometry techniques
Familiarity with GMP lab practices and electronic lab information systems
Strong attention to detail and excellent written communication skills
Ability to work independently and as part of a collaborative team
Hiring Process
10‑15 Minute Phone Interview with Region Recruiter
45‑60 Minute Virtual Interview with Manager and/or Group Leader
30 Minute Virtual Interview with Site Director
This is a full‑time, first‑shift position with a regular schedule of Monday through Friday, 8:00 AM to 4:30 PM. Flexibility may be required for occasional shift changes, weekend work, or overtime.
Compensation and Benefits The role offers a competitive hourly rate of $22.50–$27.50, along with a comprehensive benefits package that includes:
Medical, dental, and vision coverage
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Annual goal‑based bonus and merit‑based increases
About Eurofins PSS This role is part of Eurofins Lancaster Laboratories Professional Scientific Services® (PSS), our award‑winning insourcing solution. You’ll work on‑site at a client facility, fully integrated into their team while supported by Eurofins’ scientific and HR expertise.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Seniority Level Entry level
Employment Type Full‑time
Job Function Research, Analyst, and Information Technology
Referrals increase your chances of interviewing at Eurofins PSS Insourcing Solutions by 2x
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
If you’re looking for a rewarding career, apply with us today!
Job Description Make an Impact in Pharmaceutical Safety: Join Eurofins, a global leader in analytical testing, and help ensure the safety and integrity of pharmaceutical products. As part of our team, you’ll use advanced instrumentation to detect and analyze extractables and leachables; substances that could migrate from packaging or manufacturing components into drug products.
Responsibilities
Perform testing using GC-MS, LC-MS, and/or ICP-MS in a GMP-regulated lab
Analyze and interpret complex data to support clinical and commercial studies
Author technical summaries and contribute to method validation
Troubleshoot instrumentation and lab techniques
Maintain compliance with cGxP standards and regulatory requirements
Collaborate with peers and vendors in a professional lab environment
Qualifications
Bachelor’s degree in chemistry or related field with 2+ years of industry experience, or a Master’s degree with relevant experience
Hands‑on experience with mass spectrometry techniques
Familiarity with GMP lab practices and electronic lab information systems
Strong attention to detail and excellent written communication skills
Ability to work independently and as part of a collaborative team
Hiring Process
10‑15 Minute Phone Interview with Region Recruiter
45‑60 Minute Virtual Interview with Manager and/or Group Leader
30 Minute Virtual Interview with Site Director
This is a full‑time, first‑shift position with a regular schedule of Monday through Friday, 8:00 AM to 4:30 PM. Flexibility may be required for occasional shift changes, weekend work, or overtime.
Compensation and Benefits The role offers a competitive hourly rate of $22.50–$27.50, along with a comprehensive benefits package that includes:
Medical, dental, and vision coverage
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Annual goal‑based bonus and merit‑based increases
About Eurofins PSS This role is part of Eurofins Lancaster Laboratories Professional Scientific Services® (PSS), our award‑winning insourcing solution. You’ll work on‑site at a client facility, fully integrated into their team while supported by Eurofins’ scientific and HR expertise.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Seniority Level Entry level
Employment Type Full‑time
Job Function Research, Analyst, and Information Technology
Referrals increase your chances of interviewing at Eurofins PSS Insourcing Solutions by 2x
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr