Amneal Pharmaceuticals, a global leader in high-quality generic medicines, is expanding its operations in India. We are committed to producing affordable medicines with integrity, respect, and excellence. Be a part of our journey by joining our team at Pipan, Sanand Plant, Ahmedabad.
Walk-In Interview Details
- Date: Saturday, 23rd November 2024
- Time: 9:00 AM to 1:00 PM
- Venue:
Amneal Pharmaceuticals Pvt. Ltd.
Plot No: 161/1, Sanand Bavla Highway Road,
Village: Pipan, Sanand, Ahmedabad, Gujarat 382110 - Job Location: Pipan, Sanand, Ahmedabad
Injectable QA Job Openings
1. Quality Assurance – Environmental Monitoring (Microbiologist)
Designation: Trainee/Officer/Sr. Officer/Executive
Department: Environmental Monitoring (EM)
Qualifications:
- B.Sc. (Micro) / M.Sc. (Micro)
- B.Tech. (Biotech) / M.Tech. (Biotech)
Experience: 1 to 5 years in injectable/sterile manufacturing plants
Shift: Rotational shifts
Key Responsibilities:
- Environmental monitoring of clean rooms.
- Non-viable particle and compressed air/nitrogen gas monitoring.
- Personnel monitoring and record reconciliation.
- Perform line clearance activities.
2. Quality Assurance – IPQA
Designation: Officer/Sr. Officer/Executive/Sr. Executive
Department: Quality Assurance – IPQA
Qualifications:
- B.Sc. / M.Sc.
- B.Tech. (Biotech) / M.Tech. (Biotech)
Experience: 1 to 5 years
Key Responsibilities:
- Line clearance for operations like manufacturing, filling, inspection, and packing.
- Monitoring of clean rooms and air systems.
- Process validation, cleaning verification, and hold time studies.
- Perform media fill and routine batch sampling as per SOPs.
3. Quality Assurance – Validation
Designation: Officer/Sr. Officer/Executive/Sr. Executive
Department: Quality Assurance – Validation
Qualifications:
- B.Pharm / M.Pharm / M.Sc.
Experience: 1 to 7 years
Key Responsibilities:
- Execute and review validation activities for equipment and systems.
- Prepare and review protocols and reports for validation/qualification.
- Conduct risk assessments and sampling as per protocols.
- Manage change controls, deviations, CAPAs, and investigations.
- Review vendor and supplier documents related to qualifications.
Preferred Experience:
2 to 7 years in a USFDA regulatory-approved pharmaceutical organization (21 CFR compliance preferred).
What to Bring for the Interview
- Updated CV
- CTC proof, appointment and increment letters
- Last 3 months’ salary slips, bank statement
- Education certificates and mark sheets
- Aadhar and PAN card
- Passport-size photograph
How to Apply
Register for the Interview
Fill in your details online: Register Here
Can’t Attend?
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