Job Summary: Eurofins' BPT Small Molecule Method Development and Validation team is seeking a Scientist to join their team full time in Lancaster, PA. This individual will work in a dual analyst and data reviewer role. The Scientist will be able to:
* Perform various types 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).
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.
Position is full-time, 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 insurance.
* 401(k) with company match.
* Paid vacation and holidays.
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Eurofins USA BioPharma Services is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
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