Job Description

** Job Summary:** Eurofins' BPT Small Molecule Method Development and Validation team is seeking an Scientist to join their team full time in Lancaster, PA. This individual will work in a duel analyst and data reviewer role. The Scientist will be able to:

• Perform various type of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus
• Execute specialized analyses and method transfer and feasibility testing
• Troubleshoot method and instrumentation problems
• Use office and instrumentation specific computer software
• Develop and execute validation plans
• Carry out method transfers and feasibility studies
• Train technical staff
• Some travel to client sites for technical meetings could be required
• Determine if data is compliant and defendable based on industry regulations and methodology
• Verify scientific data is of sound quality following all method, industry, and client requirements where applicable
• Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations
• Review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate
• Diagnose problems, solve simple problems, and suggest solutions to complex problems in professional area
• Review methods to ensure procedures are followed
• Authorize written reports (e.g., SOP, OMC, client reports)

Qualifications

** Minimum Qualifications:**

• Bachelor's degree in chemistry, pharmaceutical science, or other related degree concentration and a minimum of 3 years of experience in a cGMP compliant industry lab.
• Master's degree in chemistry, pharmaceutical science, or other related degree concentration and a minimum of 1 year of experience in a cGMP compliant industry lab.
• Experience with HPLC and Empower
• Authorization to work in the U.S. without restriction or sponsorship

Additional Information

Position is full-time position, Monday - Friday 8:00am - 4:00pm. Candidates currently living within a commutable distance of Lancaster, PA 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 holidays

\ #LI-EB1

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.