Job 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

This role supports analytical method development and data generation to inform product development, with cross-functional collaboration and a strong emphasis on scientific rigor, safety, and continuous improvement.

Responsibilites Include: 

• Engage with scientists across Development and Manufacturing organizations to develop, evaluate, and implement robust analytical methods/technologies and control strategies to advance current analytical capabilities.
• Independently generate data to inform development activities through the use of HPLC, UHPLC, and LCMS.
• Help to develop and perform robust analytical methods (e.g., HPLC purity, potency) and collaborate with other functions to enable the successful transfer and implementation of those methods.
• Direct or facilitate material testing activities conducted by specialized characterization groups
• Perform laboratory activities with a strong emphasis on safety and technical rigor, while adhering to policies and procedures.
• Identify and exploit new scientific concepts, exhibit strong problem-solving skills, and be self-motivated to contribute across multiple projects.

Qualifications

Minimum Requirements:

• B.S. or M.S. in Analytical Chemistry, Biochemistry, Chemistry, or a related field
• (B.S. with 3–4 years of industry experience; M.S. with less than 1 year required)
• Strong hands-on experience with liquid chromatography (HPLC, UPLC, LC-MS)
• Familiarity with additional analytical techniques, including FTIR, NMR, UV-Vis, KF, ICP, DSC, TGA, and XRPD
• Solid understanding of method characterization (e.g., linearity, precision, LOD/LOQ)
• Experience with analytical instrumentation: Waters I-Class, Thermo Vanquish Flex, AKTA Pure 150 M
• Proficiency in relevant software: Empower, Xcalibur, Unicorn, BioPharma Finder
• Working knowledge of IPRP, AEX/IEX, and HILIC chromatography
• Proven ability to troubleshoot and maintain analytical instrumentation
• Strong communication, scientific problem-solving skills, and learning agility
• Effective collaborator who can manage multiple priorities and thrive in dynamic environments
• Commitment to safety and compliance
• Must be authorized to work in the U.S. without restriction or sponsorship

Preferred

Qualifications

• Experience with mass spectrometry, including oligonucleotide and RNA analysis
• Hands-on experience with RNA workflows and techniques related to RNA purification, quantification, and stability
• Familiarity with oligonucleotide characterization and analytical methods
• Knowledge of 5S or lean methodologies in laboratory settings

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
• 60 Minute Onsite Meeting with Team 

Additional Details: 

This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00 AM to 5:00 PM), with overtime required as needed. Candidates located within a commutable distance to Boston, MA are strongly encouraged to apply.

Excellent full-time benefits include:

• comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, 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 clients’ quality systems and equipment.

To learn more about Eurofins Lancaster Laboratories, please explore our website  .

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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