Quality Assurance Officer
About the Role
Roles & Responsibilities
• Prepare and review Batch Manufacturing Records (BMR)
• Prepare and review Batch Packaging Records (BPR)
• Manage and maintain Process Validation documentation
• Handle stability study documentation and related records
• Ensure compliance with GMP and quality assurance protocols
• Maintain documentation integrity and audit readiness
• Coordinate with Production and QC departments for documentation accuracy
Qualification
• B.Pharm (Bachelor of Pharmacy) / M.Pharm (Master of Pharmacy)
• B.Sc / M.Sc (Relevant Life Science qualification)
Experience
• 6 months to 2 years of experience in Pharmaceutical Quality Assurance
Skills
• Knowledge of GMP documentation practices
• Familiarity with BMR, BPR, validation protocols, and stability data
• Strong documentation and review skills
• Attention to detail and compliance awareness
• Good communication and coordination abilities
About the Organization
Noronic Pharmaceutical Pvt. Ltd. is a growing pharmaceutical company based in Ahmedabad, focused on quality-driven manufacturing practices. The organization emphasizes GMP compliance, documentation excellence, and regulatory readiness, offering strong learning opportunities for professionals building a career in pharmaceutical quality assurance.
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