Senior Executive- Filling Inj Manufacturing
Amneal Pharmaceuticals · Ahmedabad
- Experience3–7 yrs
- SalaryNot disclosed
- Work modeonsite
- Levelmid
- Posted20 Sept 2026
About Amneal Pharmaceuticals
Amneal Pharmaceuticals is hiring in Ahmedabad in pharma biotech. This role looks for around 3+ years of experience.
The role
A senior executive role in pharmaceutical manufacturing (injectable products) with 3-7 years of experience responsible for sterile production document management and GMP batch documentation, including BMRs, BPRs, master SOPs, change control, deviations, investigations, and CAPA. You will oversee aseptic manufacturing records for vial filling and vial sealing, perform line clearance, and manage cleaning/sanitization while ensuring equipment qualification and calibration, using cGMP/Good Document Practice. Required skills include filling, stoppering and sealing; equipment operation & cleaning (CIP/SIP); sterilization through autoclave; dispensing; mixing; decartoning; washing; terminal sterilization; batch documentation and record review; cleaning & line clearance; plus people management and team leadership. Location: Ahmedabad, Gujarat, India.
Full job description
Job Description
Responsible for document management like BMR’s, BPR’s, master SOP’s etc. Responsible for preparation & review of the master documents of production. Responsible to ensure UAF working in area. Responsible for the handling of change control, deviations, investigation & CAPA, etc Responsible to give training to all the subordinates, technicians and operators of the department. Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HOD’s instruction and guidance. Responsible for line clearance activity before commencing the operations. Responsible to check that all the records and logbooks related to aseptic manufacturing, vial filling and vial sealing machine. Responsible for preparation, review, revision, control and implementation of standard operating procedures of sterile manufacturing department. Responsible to ensure cleaning and sanitization of General, Controlled & Aseptic area. Inform immediately to department functional head for any observation/disturbance with respect to documents and machines found in area. Responsible for monitoring all the activities related to General, Control & Aseptic area. Responsible to ensure qualification and calibration status of equipment and instruments to avoid due/overdue.Responsible to ensure scheduled activity of respective area/equipment/instruments.Responsible to attend training as per schedule and to ensure training and work as per TNI.Follow the cGMP, Good Document Practice and discipline in the Company Premises.
Skills
Filling, stoppering and sealing | ExpertEquipment Operation & Cleaning (CIP/SIP) | ProficientDispensing | ProficientSterilization through Autoclave | ProficientMixing | ProficientDecartoning | ExpertWashing | ProficientTerminal Sterilization | ProficientGood Manufacturing Practice (GMP) | ProficientBatch Documentation and Record Review | ProficientCleaning & Line Clearance | BeginnerPeople Management & Team Leadership | Beginner
Qualifications
Qualification: M.Pharm./ B.Pharm./ M.Sc.
Exp.: 3-7 years
Candidate shall have experience in the Manufacturing of Injectable Products