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:
Responsibilities for the QC Documentation Specialist: