Document Control Specialist

1 week ago


Philadelphia, Pennsylvania, United States EPM Scientific Full time

We are seeking a highly skilled Document Control Specialist to collaborate with a reputable Pharmaceutical company in Philadelphia, PA. As a key member of the team, you will be responsible for maintaining and controlling all quality-related documents and records in compliance with regulatory requirements and company policies.

Key Responsibilities:

  • Ensure the accuracy, completeness, and compliance of all quality-related documents, including SOPs, batch records, validation protocols, and reports.
  • Collaborate with cross-functional teams to implement document control procedures and best practices.
  • Develop and maintain document management systems to support internal and external audits.
  • Provide training and support to staff on document control procedures and the use of document management systems.
  • Identify opportunities for process improvements in document control and implement best practices.

Requirements:

  • 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
  • Hybrid work arrangement
  • W2 only


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