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3 days ago
The Quality Assurance team is responsible for ensuring the quality of products throughout the manufacturing process. As a specialist, you will work closely with manufacturing teams to review and approve batch records, coordinate with on-site teams to resolve discrepancies, and analyze electronic data for reports.
Key Responsibilities:- Review and approve executed Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs)
- Coordinate with on-site teams to resolve discrepancies or missing documentation before batch release
- Analyze electronic control data, critical parameter logs, and environmental monitoring results
- Verify product label templates, proofs, and electronic versions for accuracy against specifications and regulatory standards
- Bachelor's/Master's degree in Pharmacy, Biotechnology, Microbiology, or related field
- In-depth knowledge of sterile injectable manufacturing processes and aseptic techniques
- Expertise in validation methodologies and regulatory guidelines
- Strong analytical and problem-solving skills
- Opportunity to work in a leading healthcare industry
- Competitive salary and benefits package
- Chance to develop your career in a dynamic field
Our company is looking for a highly motivated and detail-oriented individual to join our Quality Assurance team. If you have a passion for quality assurance and a strong background in pharmaceutical manufacturing, we encourage you to apply.
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