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Associate Director, Validation
| Details |
Country: USA
Location: Pearl River NY
Total applied: 33
Location: US-NY-Pearl River Company:Wyeth Job Description:
At Wyeth, we discover, develop, manufacture and market innovative medicines that are leading the way to a healthier world. In a career at Wyeth, you will be an important part of a leading research and manufacturing organization. We currently have an opening in our Validation Department for an Associate Director, Validation at our Pearl River, NY facility (located on the Rockland County, NY/Bergen County, NJ border).
As an Associate Director of Validation, you will provide oversight and guidance to validation personnel performing validation related activities within the Vaccines Fill/Finish PPU. You will act as an SME for the development of departmental policies and procedures and during regulatory inspections. You must organize and direct cross-functional interaction with manufacturing, engineering, quality control, development and regulatory personnel for validation optimization and completion as well as maintenance of the validated state in support of cGMPs. You will provide leadership including: set project priorities to meet customer needs, allocate resources, define timelines and tract projects, provide guidance on requirements to assure plant operations are in a validated state, facilitate the development of consensus among the validation, manufacturing, regulatory, and QA groups on validation study requirements and results.
You must have a BS degree in a scientific or engineering discipline. An advanced degree is preferred. You must have 10+ years of experience in validation or engineering in the pharmaceutical or biotechnology industry. You must have exceptional interpersonal, managerial and negotiating skills, be highly self-motivated, well organized, and be able to develop alternative solutions to validation issues. You must have outstanding verbal and written communication skills. You must also have a thorough understanding of biological manufacturing, engineering and quality control principles GMP. A thorough knowledge of facilities, production equipment, and regulatory guidelines is also required.
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.
For more information, visit our website at http://www.wyeth.com
Wyeth is an Equal Opportunity Employer, M/F/D/V.
Search Firm Representatives:
Please Read Carefully.
Wyeth is not seeking assistance or accepting unsolicited resumes from search firms for this employment opportunity. Regardless of past practice, all resumes submitted by search firms to any employee at Wyeth via-email, the Internet or directly to hiring managers at Wyeth in any form without a valid written search agreement in place for that position will be deemed the sole property of Wyeth, and no fee will be paid in the event the candidate is hired by Wyeth as a result of the referral or through other means. Note: Any search agreement entered into prior with Wyeth to January 2004 is hereinafter void.
Search firms are essential to the recruitment and staffing efforts at Wyeth and we value the partnerships we have built with our preferred vendors. For this reason, Wyeth has established and regularly maintains a preferred vendor list. Please note that even preferred vendors need to have a written search agreement signed by the Vice President, Strategic Staffing at Wyeth in place for the specific position in order for a fee to be paid for any candidate referrals. Requirements: Please see Job Description
Apply By Email:
Ref ID: 47663006
Leading the way to a healthier world.
For your privacy and protection, when applying to a job online: Never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction. Learn more >> |
|
Associate Director, Validation
At Wyeth, we discover, develop, manufacture and market innovative medicines that are leading the way to a healthier world. In a career at Wyeth, you will be an important part of a leading research and manufacturing organization. We currently have an opening in our Validation Department for an Associate Director, Validation at our Pearl River, NY facility (located on the Rockland County, NY/Bergen County, NJ border).As an Associate Director of Validation, you will provide oversight and guidance to validation personnel performing validation related activities within the Vaccines Fill/Finish PPU. You will act as an SME for the development of departmental policies and procedures and during regulatory inspections. You must organize and direct cross-functional interaction with manufacturing, engineering, quality control, development and regulatory personnel for validation optimization and completion as well as maintenance of the validated state in support of cGMPs. You will provide leadership including: set project priorities to meet customer needs, allocate resources, define timelines and tract projects, provide guidance on requirements to assure plant operations are in a validated state, facilitate the development of consensus among the validation, manufacturing, regulatory, and QA groups on validation study requirements and results.You must have a BS degree in a scientific or engineering discipline. An advanced degree is preferred. You must have 10+ years of experience in validation or engineering in the pharmaceutical or biotechnology industry. You must have exceptional interpersonal, managerial and negotiating skills, be highly self-motivated, well organized, and be able to develop alternative solutions to validation issues. You must have outstanding verbal and written communication skills. You must also have a thorough understanding of biological manufacturing, engineering and quality control principles GMP. A thorough knowledge of facilities, production equipment, and regulatory guidelines is also required.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.For more information, visit our website at
|
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