QC Associate

QC Associate - 2nd Shift JOB SUMMARY: Performs chemical, in-vitro, or in-vivo biological assays of clinical and/or commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process & cleaning validation samples, package samples and components. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with USP, FDA and other regulatory body requirements, Wyeth standard operating procedures, and approved license requirements. Results are compared with specifications and documented. Incumbent has a basic knowledge of fundamental technical and quality concepts and receives daily supervision.

JOB ACCOUNTABILITIES:
Performs chemical, in-vitro, or in-vivo biological assays of clinical and/or commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process & cleaning validation samples, package samples and components. Learns to recognize atypical or out-of-specifications test results, instrument malfunctions and methodology problems and participates in the investigation to resolve and correct.
Accountable for the accuracy and validity of testing results. Performs mathematical calculations, interprets results, records observations. May utilize Laboratory Information Management Systems.

EDUCATION/EXPERIENCE/REQUIREMENTS:
B.S. in Biology, Chemistry, Microbiology, Biochemistry or relevant science discipline.
M.S. (unrelated discipline)
With a B.S., 0 -1 years of relevant Quality experience.
With a M.S (unrelated).


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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