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Quality Manager III

  • Location: Meriden
  • Salary: 95.55-124.08
  • Contract hours: ZeroHour

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About the job

Position Description
Bachelors degree in engineering or technical discipline. Master
degree prefered. Experience in pharmaceutical/biopharmaceutical industry
or related industry/cGMP environment. Ability to work on strict
deadlines. Background in life science. Ability to interface with
cross-functional teams. Detail oriented. Strong working knowledge of the
FDA Quality System Regulation. Experience leading CAPA (Corrective and
Preventive Action) activities. Ability to handle multiple projects
concurrently. Well-developed communication skills, both verbal and
written. Experience in vendor/supplier management quality systems and
auditing techniques. Worksite Address1000 Research Parkway, Meriden, CT ##### ######General Comments
Monday thru Friday, Overtime as needed

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