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Regulatory Affairs Senior Specialist

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Adecco Medical & Science

2021-12-03 08:52:55

Job location Rochester, New York, United States

Job type: fulltime

Job industry: Government & Defence

Job description

Major Role Functions: Manages complex validation projects or multiple validation project activities under limited supervision, and performs assigned validation tasks such as validation product annual reviews and validated utilities re-certifications. Develops and executes equipment qualification protocols for all manufacturing, processing, and packaging equipment and facilities supporting these operations
***RELOCATION ASSISTANCE PACKAGE AVAILABLE****
***FANTASTIC BENEFITS***

Qualifications:

  • 2-5 years' pharmaceutical experience with knowledge of pharmaceutical regional regulatory procedures and legislation related to one of the following: drug development, product registration, line extension or license maintenance.
  • Experience using TrackWise, product labeling, and OTC products.


  • Equal Opportunity Employer/Veterans/Disabled

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