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Roles & Responsibilities
• Ensure compliance with current Good Manufacturing Practices (cGMP) and applicable regulatory requirements
• Manage and review QMS documentation including SOPs, batch manufacturing records, and quality reports
• Support preparation and execution of internal, external, customer, and regulatory audits
• Handle batch release activities in coordination with Production and Quality Control teams
• Identify, investigate, and implement CAPA for deviations, OOS/OOT results, and quality complaints
• Support data integrity practices and maintain accurate, traceable quality records
• Participate in continuous improvement initiatives to strengthen quality systems
Qualification
• B.Pharm or M.Pharm from a recognized university
Experience
• 1–3 years of experience in a Quality Assurance role within the pharmaceutical industry
Skills
• Strong knowledge of GMP, GLP, and regulatory guidelines (USFDA, WHO, CDSCO preferred)
• Hands-on experience with QMS, CAPA, deviations, and batch release activities
• Good documentation, audit-handling, and compliance skills
• Proficiency in MS Office and quality management systems
• Effective communication and coordination abilities
About the Company
Ceph Lifesciences Pvt. Ltd. is a well-established pharmaceutical company specializing in the manufacturing of high-quality cephalosporin-based products, driven by robust quality systems, regulatory compliance, and a commitment to excellence in pharmaceutical manufacturing.