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Associate Bio-Pharma Mfg

Thousand Oaks, CA
Top 3 Must Have Skill Sets:    

GMP/GDP experience, detail oriented, strong communication skills, able to translate data from documents to systems


Routinely perform complex electronic data entry according to Standard Operating Procedure (SOP).

Specific responsibilities include creation and validation of electronic batch records (EBR) per procedures using Manufacturing Execution System (MES) and ERP.
Responsibilities include:
- Support paper on glass manufacturing batch record process
- Translation and understanding of process specifications established by development teams into source documents (paper or electronic) utilized by production teams
-Data entry and/or verification within electronic systems
-Translation of instruction from paper sources to electronic systems
-Internal support operations (eg, data verification, document management, SOP revisions)

Must have previous biopharmaceutical manufacturing experience. Demonstrable strong communication skills (verbal and written), “Right the First Time” quality-based mindset.

Targeting Bio-Pharma background. 1+ years of drug product/manufacturing experience.
BS Engineering or Biological Sciences

"This posting is for Contingent Worker, not an FTE" 

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