
Manufacturing Quality Assurance Specialist
3 days ago
Ensure the quality and integrity of our products by overseeing the manufacturing process from start to finish.
- Responsibilities:
- Review and approve Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs) submitted from manufacturing sites for completeness, accuracy, and compliance with regulatory requirements.
- Coordinate with on-site teams to resolve discrepancies or missing documentation before batch release.
- Monitor electronic in-process control (IPC) data, critical process parameter logs, and environmental monitoring results uploaded from the site.
- Verify product label templates, proofs, and electronic versions for accuracy against specifications and regulatory standards.
- Analyze electronic data for Annual Product Quality Review (APQR) reports, identify trends or recurring issues, and prepare remote review summaries for cross-functional teams.
- Assess and approve electronic change control proposals via QMS software, evaluating potential impacts on validation, processes, and regulatory compliance.
- Conduct remote review of deviation reports, root cause analyses, and corrective action proposals, and track deviation trends for periodic reporting.
- Approve CAPA plans in the QMS system, ensuring they address identified issues with measurable effectiveness criteria, and review CAPA closure documentation to confirm adequacy of evidence.
- Review and approve Out-of-Specification (OOS) and Out-of-Trend (OOT) investigation reports submitted from the site, ensuring thorough root cause analysis and effective preventive measures.
- Ensure remote audit readiness by reviewing documentation for alignment with cGMP, US FDA, and other applicable regulatory requirements.
- Participate in virtual inspections and audits, providing requested documentation and clarifications.
- Maintain close coordination with on-site QA personnel to ensure timely resolution of documentation and compliance issues.
- Provide remote guidance to manufacturing site teams through virtual meetings, calls, and written communication.
- Education: Bachelor's/Master's degree in Pharmacy, Biotechnology, Microbiology, or related field.
- Skills: In-depth knowledge of sterile injectable manufacturing processes and aseptic techniques; Expertise in validation methodologies and regulatory guidelines; Strong analytical and problem-solving skills; Effective communication and documentation skills; Ability to manage cross-functional teams and prioritize tasks; Proficiency in QMS tools and software.
This is an exciting opportunity to join our team as a Manufacturing Quality Assurance Specialist. If you have a strong background in pharmaceutical manufacturing and quality assurance, we encourage you to apply.
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