Assistant Manager - Manufacturing & QMS
About the Role
Roles & Responsibilities
• Lead manufacturing and QMS activities
• Ensure audit readiness and regulatory compliance
• Review validation and production documents
• Manage manpower and training
• Drive process improvements
• Handle critical investigations
Qualification
• B.Pharm (Bachelor of Pharmacy)
Experience
• 8–13 years
Skills
• Leadership and team management
• Strong regulatory knowledge
• Investigation and problem-solving skills
• GMP and validation expertise
• Cross-functional coordination
About the Organization
CEPH Lifesciences supports leadership development within its regulated pharmaceutical manufacturing operations.
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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