Associate Director/Director, Quality Validation -WYETH-USA- Andover, MA

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Wyeth in Andover, MA seeks an Associate Director/Director to direct the QA Validation support for all validation activities at the Andover Manufacturing Facility relating to the validation of manufacturing systems, utilities, laboratory equipment, process automation and enterprise computer systems. Requirements: BS or equiv. in Biology, Chemistry, Engineering or related. Exp. must include at least 10 yrs in progressively responsible positions in Quality Assurance and/or validation of pharmaceutical/biopharmaceutical manufacturing processes in a cGMP environment, 5 yrs of which must include validation of computer systems in accordance with cGMP regulations.

Wyeth offers competitive compensation and benefits programs, including child-care subsidies, flex-time, business casual attire, educational assistance and professional development programs.

For more information and to apply online, please visit us at: www.wyeth.com/careers

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