Amneal Hiring Executive Manufacturing QMS Role | B Pharm Graduates Eligible
Looking for a Pharma Manufacturing Job with one of the leading pharmaceutical companies? Amneal Careers has announced an exciting opportunity for the position of Executive Manufacturing QMS and Compliance Injectable in Ahmedabad, Gujarat. This Pharma Manufacturing Job is ideal for B.Pharm and M.Pharm professionals with experience in Manufacturing QMS, Process Review, and Compliance who are looking to advance their careers through Amneal Careers.
- Job Title: Executive Manufacturing QMS and Compliance Injectable
- Location: Ahmedabad City, Gujarat, India
About the Company
Amneal Pharmaceuticals is a leading pharmaceutical company committed to delivering high-quality medicines across global markets. Through Amneal Careers, professionals have opportunities to contribute to innovative pharmaceutical manufacturing, quality, and compliance operations while building rewarding careers in the healthcare industry.
Job Description
The organization is seeking experienced professionals for Manufacturing Quality Management Systems (QMS) and Compliance activities within its sterile injectable manufacturing facility. This Pharma Manufacturing Job under Amneal Careers involves documentation management, protocol preparation, compliance monitoring, training, and continuous improvement initiatives.
Key Responsibilities
- Responsible for the preparation & review of the master documents of sterile manufacturing for the parenteral facility.
- Responsible for the preparation and review of protocols and reports based on the requirements.
- Responsible for document management and preparation, like BMR’s, BPRs, master SOPs etc.
- Responsible for the handling of change control, deviations, CAPA, investigation, etc.
- Responsible for giving training to all the subordinates, technicians, and operators of the department.
- Responsible for Audit and compliance on the manufacturing shopfloor.
- Knowledge of kaizen and continuous improvements.
Qualifications
Educational Qualification
- B.Pharm
- M.Pharm
Experience Required
- Minimum 2–5 years of experience in Manufacturing QMS / Process Review / Compliance.
Why Join This Role?
- Opportunity to work in sterile injectable manufacturing.
- Exposure to QMS, compliance, CAPA, deviations, and audit management.
- Experience in regulated pharmaceutical manufacturing environments.
- Career growth opportunities through Amneal Careers.
- Work with a globally recognized pharmaceutical organization.