Pharma Lab Scientist – GMP & Mass Spec

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. 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.

What You’Ll Do

• 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

Additional Information

What to Expect in the 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 

Additional Details:

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.

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.