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Validation Specialist I
Ref No.: 19-05346
Location: Framingham, Massachusetts
What A Great Opportunity!!!
Our client is a global biopharmaceutical company committed to healthcare solutions from prevention to treatment.  They turn scientific discoveries into medicine to improve human health.  Everyday they dedicate their most important resource, the people, to support patients and families through their health journey.

We are searching for a Validation Specialist I to assist site validation personnel through the generation and execution of select requalification and other qualification protocols as required (typically using existing protocol and report templates). Duties will also include supporting overall maintenance of the validation program (e.g. validation records management, scheduling execution activities with system owners).

Preferred Skills:
  • General knowledge of cGMP manufacturing and cGMP requirements.
  • Ability to review and perform basic statistical analysis on collected data (e.g. average, standard deviation).
  • Well-developed communication skills, both verbal and written.
  • Experience with data aquisition systems (e.g. Kaye)
  • CIP/SIP, component prep equipment (e.g. autoclave).
Education:
  • BSc/BEng plus previous experience in CQV field or equivalent combination of education and experience.
  • Experience in pharmaceutical/biopharmaceutical industry or related industry/cGMP environment.