Senior Executive Job at Amneal | BPharm/MPharm Graduates Apply Now
Looking for a stable and growth-oriented career in sterile manufacturing? This Senior Executive Job in Ahmedabad offers a strong opportunity to work with documentation, BMR/BPR review, compliance, area management, and team leadership in a modern injectable facility. Candidates with experience in aseptic processing, documentation control, and GMP practices will find this position ideal for advancing their pharma manufacturing career.
- Job Title: Senior Executive, Manufacturing Injectables
- Location: Ahmedabad City, Gujarat, India
Job Description
The Senior Executive – Manufacturing Injectables is responsible for managing key documentation activities including BMRs, BPRs, and master SOPs. The role ensures accurate preparation, review, and control of all production documents while maintaining compliance in the sterile manufacturing department
Key Responsibilities of the Pharma Job
- Manage document control including BMRs, BPRs, and master SOPs.
- Prepare and review master documents for the production department.
- Ensure proper functioning of UAF in the area.
- Handle change controls, deviations, investigations, and CAPA.
- Check and maintain all records and logbooks related to manufacturing, sterilization, and washing activities.
- Prepare, review, and update SOPs for sterile manufacturing.
- Ensure cleanliness and sanitization of general and controlled areas.
- Immediately report any issues related to equipment, documents, or processes.
- Monitor activities in general and controlled areas.
- Provide training to subordinates, operators, and technicians.
- Ensure the area is always updated with documents and cleaning status.
- Offer guidance and ensure familiarity with machines and manufacturing operations.
Qualifications required for the Pharma Job
B.Pharm / M.Pharm
Why This Role?
If you’re looking to build a long-term career in sterile and injectable manufacturing, this Senior Executive role at Amneal offers the perfect growth platform. It gives you hands-on responsibility in documentation management, GMP compliance, aseptic operations, and controlled-area oversight—all essential skills for stepping into higher leadership roles in sterile production. With exposure to BMR/BPR review, deviation handling, CAPA, and area supervision, this opportunity helps you strengthen both technical expertise and managerial capabilities in a world-class injectable facility.
