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