QA Documentation Specialist – GMP & Compliance

Acrotech Biopharma Inc. is seeking a QA Documentation Specialist to support Quality Assurance functions under the Sr. Director of QA. You will organize GxP documents, assist with purchase orders and budgets, and help oversee contracted manufacturers and marketing partners in a document-centric role.
The role emphasizes proper formatting, organization, and retrievability of documents, with potential expansion into other QA tasks. Travel is expected to be limited, <5%.

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