Pharma Jobs in India: Amneal is Hiring in Ahmedabad | Apply Now for Senior Executive Jobs
Are you excited to progress your career and seeking for Pharma Jobs in India? Join as a Senior Executive – Manufacturing in Ahmedabad, Gujarat, and play a key role in sterile manufacturing operations, packaging, and inspection. Ideal for B.Sc, B.Pharm, M.Sc, or M.Pharma graduates with 2–7 years of experience, this Senior Executive job role involves planning, executing, and monitoring production activities while ensuring compliance with cGMP, Good Documentation Practices, and standard operating procedures (SOPs).
Job Details:
- Job Position: Senior Executive – Manufacturing
- Location: Ahmedabad City, Gujarat, India
- Job Type: Full-Time
- Job ID: 4981
About the Company:
Amneal is a leading pharmaceutical manufacturer based in Ahmedabad, Gujarat, specializing in sterile manufacturing, packaging, and inspection. With a strong focus on quality, compliance, and operational excellence, the organization adheres to cGMP and Good Documentation Practices (GDP) to ensure the production of safe and effective medicines.
Amneal fosters a culture of continuous learning, process improvement, and employee development, empowering professionals to contribute to high-quality manufacturing operations. Employees are encouraged to innovate, maintain high standards, and deliver excellence in sterile pharmaceutical production, making the organization a trusted name in the industry.
Education & Experience:
B.Sc., B.Pharm, M.Sc., M.Pharm with 2–7 years of experience in a sterile manufacturing plant.
Key Responsibilities for Senior Executive Job Role:
- Prepare monthly and daily packaging plans based on material availability and production requirements.
- Maintain self-hygiene and adhere to all safety and hygiene protocols.
- Attend scheduled training sessions and ensure compliance with Training Needs Identification (TNI).
- Operate according to standard operating procedures (SOPs) in the sterile manufacturing department.
- Prepare, review, revise, control, and implement SOPs for the General Area of Sterile Manufacturing.
- Prepare Batch Production Records (BPR) accurately.
- Ensure all equipment and production lines are validated and calibrated.
- Check and maintain records and logbooks related to packaging and inspection areas.
- Provide training to subordinates, technicians, and operators in the department.
- Follow cGMP, Good Documentation Practices, and discipline in all department activities.
- Handle document control for packing and inspection processes.
- Monitor and ensure smooth execution of all packing and inspection activities.
Skills:
Knowledge of sterile manufacturing processes, SOP compliance, packaging, inspection, and cGMP standards
