Key Responsibilities:
In-Process Quality Assurance (IPQA) and manufacturing operations.
Batch Manufacturing Record (BMR) review and documentation control.
Quality Management Systems (QMS) and SOP compliance.
Validation and qualification activities.
Internal audits, regulatory inspections, and compliance.
Implementation of cGMP and regulatory requirements (WHO/TGA).
Qualifications & Skills:
B.Sc. / M.Sc. / B.Pharm. / M.Pharm.
Valuable knowledge of cGMP guidelines, 21 CFR Part 210/211, and ALCOA+ data integrity principles.
Robust documentation skills and attention to detail.
📌 Chemist Qa Bhongir (India)
🏢 Prathyak Laboratories
📍 India
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