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QA Documentation Specialist – GMP & Compliance
Job in
Jersey City, Hudson County, New Jersey, 07390, USA
Listed on 2026-07-16
Listing for:
Acrotech Biopharma inc.
Full Time
position Listed on 2026-07-16
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist
Job Description & How to Apply Below
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,
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