Document Control Specialist
EPM Scientific - philadelphia, PA
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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 week12 Months initial contractStart Date: ASAPPhiladelphia, PA (Hybrid)W2 only
Created: 2024-09-26