Qa Documentation ( Pharma industry)
Updated: May 17, 2024 10:19 AM GMT
Shining Placement
Roorkee, UttarakhandThe Quality Assurance Documentation Specialist plays a pivotal role in ensuring the accuracy, integrity, and compliance of all documentation within the pharmaceutical quality management system. This position is responsible for managing document control processes, maintaining regulatory compliance, and supporting internal and external audits. The ideal candidate possesses a strong understanding of pharmaceutical documentation requirements, meticulous attention to detail, and the ability to collaborate effectively with cross-functional teams.
• Develop, implement, and maintain Standard Operating Procedures (SOPs) related to document control and management.
• Oversee the creation, revision, review, approval, distribution, and archival of pharmaceutical documents, including batch records, protocols, reports, and quality records.
• Ensure all pharmaceutical documents adhere to regulatory requirements, including FDA regulations, ICH guidelines, and cGMP standards.
• Collaborate with... More Detail
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