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We are searching for a Quality Control Documentation Specialist to join the chemistry team at a rapidly growing, fast-paced biotech company in Andover, MA.

 

The QC Documentation Specialist will be responsible for the data review for the release of raw materials, in-process and finished formulations following SOP’s, and compile data for documentation of test procedures, perform investigations and prepare reports.

 

This position offers a generous benefit package,  including paid time off, health insurance, Long Term Incentives and 6% matching 401k plan.

 

Requirements for the QC Documentation Specialist:

 

  • Bachelors of Science degree in Chemistry or other relevant science degree
  • 3+ years relevant industry experience
  • GC, GC/MS, NMR or HPLC experience a plus
  • GMP and or ISO experience preferred
  • Biovia LES/LIMS system hands-on experience preferred
  • The ability to manage multiple competing priorities
  • Strong communications skills; oral, written and electronic.
  • Ability to work effectively both independently and collaboratively in a team environment 

 

Responsibilities for the QC Documentation Specialist:

  • Document test data as required
  • Follow documented procedures
  • Review data for release of GMP/ISO and/or non-regulated materials
  • Write test procedures and SOP’s
  • Perform investigations
  • Prepare reports
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