
Senior Quality Assurance Specialist
5 days ago
Job Overview:
We are seeking a skilled professional to join our team in IPQA. The ideal candidate will have a strong background in pharmaceutical manufacturing and experience in real-time monitoring, line clearance, and in-process checks.
Key Responsibilities:
- Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR)
- Ensure compliance with GMP and regulatory standards
- Handle deviations, documentation, and audit support
- Assist in the development of new processes and procedures
Requirements:
- Bachelor's degree in a relevant field or higher
- At least 5 years of experience in IPQA, BMR/BPR review, and pharmaceutical manufacturing
- Strong analytical and problem-solving skills
- Excellent communication and teamwork skills
What We Offer:
- A dynamic and supportive work environment
- Opportunities for professional growth and development
- A competitive salary and benefits package
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