QC Documentation Specialist

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