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Process Supervisor
| Details |
Country: USA
Location: Andover MA
Total applied: 40
Location: US-MA-Andover Company:Wyeth Job Description:
Job Summary:
Reporting to the Operations Manager, the Process Supervisor is responsible for the shift operations occurring in the start-up and operation of a cGMP Manufacturing Suite at the Andover Manufacturing Facility (AMF).
Duties & Responsibilities:
Provide leadership to staff
Oversee and proactively address operation and employee relations issues
Facilitate staff development
Oversee highly automated process manufacturing operations; mechanically inclined.
Write, Review, Proofread, Edit, and Archival of Department GMP Documents and SOPs
Participate on equipment startup teams
Schedule in-suite work and coordinate workloads
Ensure cGMP compliance
Develop electronic work instructions
Ensure a safe work environment
Close out documentation required for product disposition
Achieve Wyeth BioPharma's manufacturing objectives
Supervise a work group of 4 -12 technicians.
Requirements:
High School Diploma, Biotechnology Certificate, or equivalent. BS in Life Sciences highly desirable.
Minimum of 6 years in a Biopharmaceutical or Pharmaceutical manufacturing environment, 2 of which were spent in a
supervisory or leadership role, or equivalent. Possess the ability to work independently, be proactive, and a team player.
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: 47919400
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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 >> |
|
Process Supervisor
Job Summary: Reporting to the Operations Manager, the Process Supervisor is responsible for the shift operations occurring in the start-up and operation of a cGMP Manufacturing Suite at the Andover Manufacturing Facility (AMF).Duties & Responsibilities:
Provide leadership to staff
Oversee and proactively address operation and employee relations issues
Facilitate staff development
Oversee highly automated process manufacturing operations; mechanically inclined.
Write, Review, Proofread, Edit, and Archival of Department GMP Documents and SOPs
Participate on equipment startup teams
Schedule in-suite work and coordinate workloads
Ensure cGMP compliance
Develop electronic work instructions
Ensure a safe work environment
Close out documentation required for product disposition
Achieve Wyeth BioPharma's manufacturing objectives
Supervise a work group of 4 -12 technicians.Requirements:
High School Diploma, Biotechnology Certificate, or equivalent. BS in Life Sciences highly desirable.
Minimum of 6 years in a Biopharmaceutical or Pharmaceutical manufacturing environment, 2 of which were spent in a
supervisory or leadership role, or equivalent. Possess the ability to work independently, be proactive, and a team player.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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