QA Specialist I

QA Specialist I JOB SUMMARY: The primary responsibilities include, but are not limited to, quality support of sampling, testing and disposition of production materials. Ensure documentation related to production materials complies with cGMP, regulatory, and Wyeth requirements. The incumbent uses a working knowledge of GMP regulations and Wyeth procedures and policies, and relevant quality techniques, complete projects. Learns and executes defined quality tasks efficiently and reproducibly.
JOB ACCOUNTABILITIES:
Reviews quality documentation to ensure compliance with cGMP standards and internal procedures.
Tracks status of regulatory, internal audit, and external audit commitments, investigations, and change controls.
Participates in regulatory, internal, and external audits as needed. Provides information for vendor, contractor, and contract lab audits as appropriate.
Identifies basic technical problems and begins to develop problem-solving skills independently and in consultation with supervisor.
Reviews and edits compliance related documents and internal procedures as required.
Ensures production materials meet defined quality standards prior to disposition.
Carries out technical and administrative duties as assigned.
Inputs data into Integrated Management Reports, Annual Product Reviews, LIMS, and SAP as appropriate
EDUCATION/EXPERIENCE/REQUIREMENTS:
BS w/ 2 years.
Entry for related MS.
BS in Chemistry or relevant science discipline with 2 years experience in Quality or a bio/pharmaceutical industry.
Entry for related MS.



Wyeth offers competitive compensation and benefits programs including stock
options, child-care subsidies, flex-time, business casual attire,
educational assistance and professional development programs. Please
forward your resume with salary requirements and job reference code to the
address below.

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