Quality control associate

The opportunity

The Raw Materials Analysis group strives to deliver creative medicines to patients through performance of sampling, testing and release of controlled materials within a GxP-compliant QC laboratory to support development of biological products manufactured in a GMP production facility.

The incumbent should possess a practical understanding of bio-pharmaceutical drug development and GxP requirements as knowledge of local, regional and global regulatory compliance (ICH, GMP, EPA, OSHA, DEA, etc) are integral responsibilities of this position.

Travel Requirements : none

Location : West Chester, PA

RELOCATION ASSISTANCE AND WORK VISA SPONSORSHIP IS NOT AVAILABLE

How you’ll spend your day

• Sampling, testing and release of raw materials (e.g. executing testing, results analysis, peer review of data, etc.)
• Method qualification and validation, as required.
• Laboratory investigation (e.g. deviations, Out of Specification, Out of Trend results), Change Controls, Deviations and CAPA (Corrective Action / Preventive Action) management, as required.
• Management of standard operating procedures, work instructions, protocols, reports, and standard practices.
• Actively contribute to the maintenance of a compliant, clean, safe working environment (e.g. records, instruments, equipment, materials, reagents, quality systems etc.

in the laboratories by maintaining compliance with applicable ICH, GMP and safety regulations.

Participate in internal and external audits, inspections, regulatory assessments, and filings.

Your experience and qualifications

Quality Control Associate (9)

Bachelor's degree, preferably in Chemistry, Biochemistry or Biology, from an accredited college or university 1 year in the (Bio)pharmaceutical industry with Raw Material Testing and sampling.

Senior Quality Control Associate (10)

Bachelor's degree, preferably in Biochemistry or Biology, from an accredited college or university 3 years of experience in the (Bio)pharmaceutical industry with Raw Material Testing and sampling -OR- Master's degree, preferably in Biochemistry or Biology, from an accredited college or university 1 year of experience in the (Bio)pharmaceutical industry with bioassays / potency assays

Bachelor's degree, preferably in Biochemistry or Biology, from an accredited college or university 5 years of experience in the (Bio)pharmaceutical industry with Raw Material Testing and sampling -OR- Master's degree, preferably in Biochemistry or Biology, from an accredited college or university 3 years of experience in the (Bio)pharmaceutical industry with Raw Material Testing and sampling.

Enjoy a more rewarding choice

We offer a competitive benefits package, including Medical, Dental, Vision, and Prescription coverage starting on the first day.

We also offer Disability and Life Insurance, Paid Time Off, 13 paid Holidays, 6% match on the 401(k), Employee Stock Purchase Plan, and Tuition Assistance

Last updated : 2024-06-14

Salary : $51,400 - $65,000