Upstream Manufacturing Associate- GMP Ops (1320)

By Posted in - on June 16th, 2017 0 Comments
Adante Staffing Inc. Published: July 28, 2017

Description

Our client is a well known BioPharma company located north of Boston. Stability, Great Benefits, and Corporate Culture .....

GMP Manufacturing Associate, Upstream  (Direct Hire) 

Primary Responsibilities:

  • Ensure upstream (Fermentation)  operations are conducted in compliance with cGMP standards and applicable regulations.
  • Support the upstream technology transfer process for all products being transferred to GMP production.
  • Support the execution of the initial and ongoing equipment validation requirements.
  • Review manufacturing batch records upon completion. Initiate and investigate process deviations and resulting CAPA plan.

Qualifications and Experience:

  • Requires a minimum of a BS in the sciences with >3 years working in a cGMP controlled environment.
  • Substantial hands-on experience working in upstream processing environments according to GMP principles.
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