Job Description

Seeking a scientist to perform analytical testing for biologic product release and characterization in a cGMP/GLP environment. Responsibilities include routine testing, documentation, troubleshooting HPLC/UPLC/CE methods, and ensuring compliance.

Responsibilities Include:

• Contributes as part of a team of AD scientists towards execution of various analytical methods to support biological therapeutic product release and characterization testing in a compliance-based environment.
• Independently performs routine testing such as but not limited to SEC, CEX, RP, P20, P80, CE, iCE, cIEF, CE-SDS, Titer, Peptide, and Glycan mapping - using established Test Methods, including associated protocol/report documentation and presentations.
• Conducts work in compliance with cGMP/GLP, safety, and regulatory requirements.
• Responsible for working on other non-lab-based tasks from time to time if assigned.
• Demonstrate 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.
• Demonstrate HPLC, UPLC, and/or CE troubleshooting capabilities.

Qualifications

The Ideal Candidate will Have:

• Experience with ELISA techniques
• Ability to quickly learn new techniques
• Strong multitasking and organizational skills
• Attention to detail with accurate record-keeping
• Ability to follow instructions and adhere to company policies

Minimum Qualifications:

• Bachelor’s or Master’s in Cell and Molecular Biology, Biochemistry, Pharmaceutical, or other science-related degree concentration
• Equivalent directly related work/internship experience with HPLC/UPLC required.
• Knowledge of principles of HPLC/UPLC/CE and theories of relevant techniques and a basic understanding of industry practices and standards required
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Additional Information

What to Expect in the Hiring Process:

• 10-15 Minute Phone Interview with the Region Recruiter
• 45-60 Minute Virtual Interview with the Manager and/or Group Leader
• 30 Minute Virtual Meeting with the Site Director

Additional Details:

The position is full-time, Monday-Friday from 8 am-5 pm. Candidates living within a commutable distance of Lexington, Massachusettes, and the surrounding areas are encouraged to apply.

• Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holiday

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 a 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.

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

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