Roles & Responsibilities
• Implement and maintain Quality Management Systems (QMS) as per GMP and regulatory guidelines
• Execute process, equipment, and cleaning validation activities
• Prepare, review, and approve validation protocols and reports
• Handle deviations, change controls, CAPA, and quality investigations
• Participate in internal audits, regulatory inspections, and compliance activities
• Ensure proper documentation control and data integrity
• Train personnel on SOPs, GMP practices, and quality procedures
• Support continuous improvement and quality risk management initiatives
Open Positions
• Assistant Manager – QA
• QMS Senior Officer
• QMS Officer
• Validation Executive
• Validation Officer / Senior Officer
Qualification
• B.Pharm / M.Pharm
• MSc (Microbiology / Biotechnology / Chemistry) or equivalent
Experience
• 2 to 10+ years of relevant experience in QA, QMS, or Validation
• Experience level varies depending on the role applied for
• Prior exposure to regulated pharma manufacturing preferred
Skills
• Strong knowledge of GMP, GLP, WHO, USFDA, EDQM guidelines
• Hands-on experience in validation and quality systems
• Documentation, data analysis, and audit-handling skills
• Familiarity with QMS tools and regulatory inspections
• Good communication, problem-solving, and attention to detail
About the Organisation
Ceph Lifesciences Pvt Ltd is a growing pharmaceutical company with manufacturing operations across India, including Himachal Pradesh, and a registered base in Telangana. The company focuses on delivering high-quality pharmaceutical products while maintaining strong compliance with global regulatory standards.
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