Amneal Pharmaceuticals is conducting a virtual drive for experienced candidates in Quality and Manufacturing functions at its SEZ Matoda, Ahmedabad location. The opportunity is suitable for candidates with relevant experience in an injectable regulated plant and hands-on exposure to quality control, quality assurance, aseptic manufacturing, packing or related operations.
The Microsoft Teams interview link and exact timeslot will be shared with shortlisted candidates only. Interested candidates need to apply online and register for the virtual walk-in by scanning the QR code provided in the hiring banner.
1. Quality Control Roles
Job Overview
The Quality Control department is hiring for QC Analyst and QC QMS positions. These roles are focused on analytical testing, documentation, compliance and quality management activities in a regulated injectable manufacturing environment.
| Department | Quality Control |
| Designation | QC Analyst, QC QMS |
| Qualification | B.Sc. / M.Sc. / B.Pharm / M.Pharm |
| Experience | 4 – 9 Years |
| Job Location | SEZ Matoda, Ahmedabad |
Responsibilities
- Perform quality control analysis and documentation activities as per regulated plant requirements.
- Support analytical testing, stability and compliance-related quality systems.
- Handle QC documentation, investigation and compliance activities as applicable to the role.
Qualifications
- B.Sc., M.Sc., B.Pharm or M.Pharm qualification is required.
- Relevant experience in an injectable regulated plant is required.
Key Skills and Experience Required
- For QC Analyst: Analysis of RM-PM or IP-FP and handling of HPLC Waters and SHIMADZU, GC Agilent is must.
- LIMS calibre and Master Preparation.
- For QC QMS: Investigation of Deviation, Incident, OOS and OOAL/OOT.
- CAPA and Change Control Management, Effectiveness.
- Quality Risk Management (QRM).
- Audit Handling and Inspection Readiness.
2. QA – IPQA EM Roles
Job Overview
Amneal is also hiring Officer / Executive level candidates for QA – IPQA EM. The role requires candidates who can work in environmental monitoring and aseptic area monitoring activities. Working in 3 shifts is required for this role.
| Department | QA – IPQA EM |
| Designation | Officer / Executive |
| Qualification | B.Pharm / M.Sc / M.Pharm |
| Experience | 2 – 7 Years |
| Job Location | SEZ Matoda, Ahmedabad |
Responsibilities
- Carry out IPQA and environmental monitoring activities as per site requirements.
- Support aseptic area behaviour monitoring and personnel monitoring activities.
- Maintain compliance with quality and monitoring procedures.
Qualifications
- B.Pharm, M.Sc or M.Pharm qualification is required.
- Relevant injectable regulated plant experience is required.
Key Skills and Experience Required
- Environment monitoring.
- Aseptic area behaviour monitoring.
- Personnel monitoring.
- Trend preparation.
- NVPC monitoring and viable monitoring.
3. Injectable Manufacturing Roles
Job Overview
The Injectable Manufacturing department is hiring for Production and Packing roles. Open designations include Aseptic Filling and Packing Operator at Assistant / Associate level, and Supervisors at Officer / Executive level.
| Department | Injectable Manufacturing – Production and Packing |
| Designation | Aseptic Filling and Packing Operator, Supervisors |
| Qualification | Diploma / B.Sc. / ITI / B.Pharm / M.Sc / M.Pharm |
| Experience | 4 – 9 Years for Operator and Supervisor role |
| Job Location | SEZ Matoda, Ahmedabad |
Responsibilities
- Support sterile, parenteral and aseptic production or packing operations.
- Work on filling, sealing, filtration, batch manufacturing, packing and visual inspection activities as per assigned role.
- Follow applicable manufacturing, safety and compliance practices in an injectable regulated plant.
Qualifications
- Diploma, B.Sc., ITI, B.Pharm, M.Sc or M.Pharm qualification is required as applicable to the role.
- Hands-on experience in sterile / parenteral / aseptic operations is required.
Key Skills and Experience Required
- Sterile / Parenteral / Aseptic operations.
- Filling, sealing and filtration.
- Batch manufacturing.
- Packing and visual inspection.
- Line exposure: Ophthalmic, Vial, PFS, LYO, Cartridges, Filling Machine with Isolator and C-RABS Technology.
Virtual Drive Schedule
| Quality Virtual Drive | 9th October 2026, Friday |
| Manufacturing Virtual Drive | 10th October 2026, Saturday |
| Time | 09:00 AM to 03:00 PM |
| Interview Platform | Microsoft Teams link and exact timeslot will be shared with shortlisted candidates only |
How to Apply
Interested candidates can apply online and register for the virtual walk-in by scanning the QR code provided in the hiring banner.


