QMS Officer - Production Oral
About the Role
Roles & Responsibilities
• Manage deviation, CAPA, and change control systems
• Prepare and review SOPs and QMS documents
• Support internal and external audits
• Ensure compliance with GMP and data integrity
• Maintain document control systems
• Track training and compliance metrics
Qualification
• B.Pharm (Bachelor's of Pharmacy)
Experience
• 2–5 years
Skills
• Strong knowledge of QMS systems
• Experience in deviation and CAPA handling
• Audit readiness and documentation skills
• Regulatory compliance knowledge
• Analytical mindset
About the Organization
CEPH Lifesciences maintains robust quality systems aligned with regulatory requirements to ensure product safety and compliance.
Walk-in Interview Details
Timing: 09:00 AM to 04:00 PM (Monday to Saturday)
Venue: CEPH Lifesciences, Village Bhatoli Kalan, Adjoining Jhar Majri, Baddi, Himachal Pradesh – 174103, India
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