at our Kathua facility. The ideal candidate will be responsible for managing and enhancing the
Quality Management System
(QMS) in compliance with
GMP, WHO, and ICH guidelines
to ensure product quality and regulatory readiness.
Key Responsibilities:
Implement and maintain QMS documentation, including SOPs, change control, deviation, CAPA, and quality risk management
Ensure compliance with regulatory standards and internal quality procedures
Conduct and support internal and external audits, prepare audit responses, and follow up on CAPA implementation
Manage document control and version control systems efficiently
Review and maintain training records and support quality improvement initiatives
Coordinate with cross-functional teams such as Production, QC, and R&D to ensure quality compliance
Report QMS performance to the management and recommend improvements
Candidate Requirements:
Education: B.Pharm / M.Pharm / M.Sc in Chemistry or Pharmaceutical Sciences
Experience: Minimum 3-5 years of relevant experience in pharmaceutical QMS
Knowledge of cGMP, WHO-GMP, ICH, and ISO 9001 standards
Strong analytical skills with attention to detail
Good communication and interpersonal skills
Proficient in MS Office and QMS-related documentation systems
Why Join Us?
Be part of a WHO-GMP certified and rapidly growing pharmaceutical manufacturing company
Work in a regulatory-compliant and professional environment
Opportunities for career growth, skill enhancement, and learning
Job Type: Full-time
Pay: ?25,000.00 - ?50,000.00 per month
Supplemental Pay:
Performance bonus
Yearly bonus
Work Location: In person
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