Eurofins
Scientist - Small Molecule Analytical Chemistry
Eurofins, Lancaster, Pennsylvania, United States, 17601
Scientist - Small Molecule Analytical Chemistry
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 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 Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
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 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 Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.