Evening Pharma Document Control Specialist

Amneal Pharmaceuticals LLC

Piscataway Township (NJ)

Sur place

USD 28 000 - 34 000

Plein temps

Il y a 13 jours
Générateur de candidature

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Avantages offerts par ce poste

Bonus opportunity
Health benefits
401(k) matching
Well-being programs

Résumé du poste

Amneal is seeking a Document Control Specialist for a 2nd shift role in a pharmaceutical production facility. You will administer document control processes, ensure compliance, collaborate with QA, QC and Production, and manage electronic and paper systems to maintain accuracy and integrity of documents such as COAs, specs, methods, and SOPs.

Responsibilities include distributing approved docs, tracking approvals, preparing PBRs and batch records, maintaining training records, and coordinating

Qualifications

  • High School or GED is required.
  • Associate degree is preferred.
  • Experience in manufacturing is preferred.

Responsabilités

  • Manage document control processes thru electronic systems and/ or paper base systems; distribute approved documentation to appropriate personnel and track receipt.
  • Maintain lists and postings for electronic and hard copy; manage databases in Document Control and training records.
  • Perform data entry and management in systems and maintain print/soft copies for all documents.
  • Collaborate with QA, QC and Production to maintain up-to-date Document Control Systems.
  • Store, archive, and retrieve documents such as COAs, specs, methods, protocols, and reports.
  • Prepare and distribute PBRs, Packaging Batch Records, SOPs and other controlled documents.

Connaissances

cGMP
MS Word
Excel
Access

Formation

High School or GED
Associate degree

Description du poste

Amneal is seeking a Document Control Specialist for a 2nd shift role in a pharmaceutical production facility. You will administer document control processes, ensure compliance, collaborate with QA, QC and Production, and manage electronic and paper systems to maintain accuracy and integrity of documents such as COAs, specs, methods, and SOPs.

Responsibilities include distributing approved docs, tracking approvals, preparing PBRs and batch records, maintaining training records, and coordinating

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