The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

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.

If you’re looking for a rewarding career, apply with us today!  

• Contributes as part of a small team towards the execution and development of various analytical methods to support biological therapeutic characterization testing in a research-based environment.
• Works closely with adjacent team members to collaborate and reach collective goals related to study designs and organization of shared lab space.
• Method development and execution related work, as well as associated documentation and regular assay troubleshooting.
• Performs protein characterization testing as assigned, such as glycan analysis and disulfide mapping, and other types of analyses to include proteomics, intact protein, subunit, and peptide mapping.
• Computer competency is essential with emphasis on spreadsheet-based software.
• Uses the Protein Metrics software (Byos or Byosphere) to view and analyze MS data.
• Supports drug development projects and regulatory submissions, such as IND and BLA filings.
• Understands and applies the advanced scientific principles, theories and concepts, practices and standards for product development.
• Conducts work in compliance with GLP, safety and regulatory requirements.
• Provides routine updates to client via progress presentations and is responsible for following up on project deadlines and other agreed objectives.
• Demonstrates independent judgment in technique and method selection, protocol and study design and execution, data analysis and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives.

• Candidate must have a degree in Chemistry (Analytical or Organic), Biochemistry, Pharmaceutical, or other biological/analytical discipline, along with the following experience in biotechnology, pharmaceutical, or related environment:
• BS (8-12 yrs exp); Engineer (6-10 yrs exp); MS (6-10 yrs exp); or PhD (2-5 yrs exp):  
  • Experience working with one or more oft he following methods: intact protein, subunit, and peptide mapping analyses, proteomics, etc., is a must.
  • Hands-on LC-MS experience using a Thermo Orbitrap mass spectrometer is a must.
  • Experience working with Mass Spectroscopy instrumentation and software like Protein Metrics (Byos or Byosphere) is preferred.
  • Experience working with one or more of following protein characterization methods: glycan analysis, disulfide mapping, etc is a plus
• Understanding of basic scientific principles and theories of one of the techniques within LCMS/MS and protein characterization techniques is a must
• Knowledge of theories, principles and techniques of relevant scientific areas and basic understanding of industry practices and standards is required
• Strong computer, scientific, and organizational skills
• Excellent communication (oral and written) and attention to detail
• Ability to work independently and as part of a team, 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
• Authorization to work in the United States indefinitely without restriction or sponsorship

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
• 45-60 Minute Meeting Onsite to Meet the Team 

Position is Full Time, Monday-Friday, First Shift, Monday through Friday from 8 am-5 pm Candidates currently living within a commutable distance of Lexington, MA, are encouraged to apply

Excellent full-time benefits include: 

• Medical Coverage: Comprehensive medical insurance options
• Dental & Vision: Full dental and vision coverage available
• Life & Disability Insurance: Employer-sponsored plans
• Retirement: 401(k) plan with company match
• Paid Time Off: Vacation days, paid holidays, and additional PTO options
• Compensation: $100,000 - $107,000 annually  

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