Responsibilities
* Perform various types of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, 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.
* Document work to meet GMP compliance.
* Perform tests accurately.
* Troubleshoot method and instrumentation problems.
* Use office and instrumentation‑specific computer software.
* Produce written reports (e.g., SOP, OMC, client reports).
* Develop and execute validation plans.
* Carry out method transfers and feasibility studies.
* Train technical staff.
* Travel to client sites for technical meetings (approximately 25% travel).
Qualifications
* Authorization to work in the United States indefinitely without restriction or sponsorship.
* 1‑2 years of transferable laboratory experience.
* Experience using EMPOWER and HPLC in industry.
* Experience with validation in industry.
* Bachelor’s or Master’s degree in chemistry or a related field (or equivalent).
* 3 years related pharmaceutical experience in a cGMP environment.
Work Schedule
Full‑time, first shift, Monday – Friday, 8 am – 4 pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. This position is NOT remote.
Benefits
* Comprehensive medical, dental, and vision coverage.
* Life and disability insurance.
* 401(k) with company match.
* Paid vacation and holidays.
#J-18808-Ljbffr