Teva Quality Control Associate - Raw Materials GMP On-site 

United States, Pennsylvania, East Bradford Township 

539999838

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.

none

West Chester, PA

• 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.

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

Quality Control Associate Scientist (11)

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.

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