Document Control Specialist

2 months ago


Philadelphia, United States EPM Scientific Full time

We are working closely with a reputable Pharmaceutical company that are looking for a Document Control Specialist to join their team. You will be responsible for managing and maintaining all controlled documents and records in compliance with regulatory requirements and company policies.


Responsibilities:

  • Maintain and control all quality-related documents, including SOPs, batch records, validation protocols, and reports.
  • Ensure all documents are compliant with regulatory standards (e.g., FDA, EMA) and company policies.
  • Review and approve documents for accuracy, completeness, and compliance before release.
  • Assist in the training of staff on document control procedures and the use of document management systems.
  • Support internal and external audits by providing necessary documentation and records.
  • Identify opportunities for process improvements in document control and implement best practices.


Qualifications:

  • Bachelor’s degree in a relevant field (e.g., Life Sciences, Quality Management).
  • Minimum of 3 years of experience in document control within the pharmaceutical or biotech industry.


Contract Details:

  • 40 Hours per week
  • 12 Months initial contract
  • Start Date: ASAP
  • Philadelphia, PA (Hybrid)
  • W2 only


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