Looking for a pharmaceutical job in Quality Control? Amneal Pharmaceuticals has announced a walk-in interview for experienced professionals at its Rajoda manufacturing facility near Ahmedabad, Gujarat. Candidates having experience in OSD regulated plants are invited to attend the interview for multiple Quality Control and QMS Investigation positions.
If you have relevant experience in analytical testing, HPLC/UPLC, regulatory documentation, or QMS investigations, this could be a great opportunity to join one of the leading pharmaceutical companies.
Job Overview
Company Name: Amneal Pharmaceuticals
Job Type: Walk-In Interview
Interview Date: 05 July 2026 (Sunday)
Interview Time: 09:00 AM to 01:00 PM
Walk-In Venue:
Near Hotel Kankavati,
Village Rajoda,
Ahmedabad โ 382220,
Gujarat, India
Job Locations:
- Rajoda
- SEZ-Matoda
Industry: Pharmaceutical Manufacturing (OSD Regulated Plant)
Important Note: No vacancies are available in the Microbiology section.
Available Positions
1. Quality Control (Topical)
Designation
- Analyst
- Senior Analyst
Qualification
- B.Pharm
- M.Sc.
Experience
- 01โ05 Years
2. Quality Control
Designation
- Analyst
- Senior Analyst
Qualification
- B.Pharm
- M.Sc.
Experience
- 01โ05 Years
3. Quality Control (QMS โ Investigation)
Designation
- Supervisor
- Reviewer
Qualification
- B.Pharm
- M.Sc.
Experience
- 07โ12 Years
Roles & Responsibilities
Depending on the selected department, candidates will be responsible for:
- Perform analysis of ointment, cream, gel, solution, raw materials, finished products and stability samples.
- Operate HPLC, UPLC, GC, UV, IR, pH, viscosity, dissolution and assay testing instruments.
- Ensure compliance with cGMP, GLP, ALCOA+, data integrity and laboratory documentation.
- Handle calibration and routine maintenance of analytical instruments.
- Support OOS, OOT, deviation and laboratory investigation activities.
- Conduct QMS investigations and audit trail reviews.
- Maintain accurate analytical records and regulatory documentation.
Required Qualifications
Candidates should possess any of the following qualifications:
- B.Pharm
- M.Sc.
Required Skills
Applicants should have knowledge of:
- HPLC
- UPLC
- GC
- UV Spectroscopy
- IR Spectroscopy
- Dissolution Testing
- GLP & cGMP Practices
- ALCOA+
- Data Integrity
- OOS/OOT Investigations
- CAPA
- Laboratory Documentation
- Audit Trail Review
Experience Required
- Quality Control (Topical): 1โ5 Years
- Quality Control: 1โ5 Years
- QMS Investigation: 7โ12 Years
Note: Relevant experience in an OSD regulated pharmaceutical plant is required.
Salary & Benefits
Selected candidates can expect:
- Estimated Salary: โน3.5 LPA โ โน12 LPA (depending on role, experience and company policy)
- Opportunity to work in a regulated pharmaceutical manufacturing environment.
- Professional growth and learning opportunities.
- Exposure to advanced analytical laboratories and quality systems.
- Employee benefits as per company policies.
How to Apply
Eligible candidates should attend the walk-in interview with:
- Updated Resume
- Educational Certificates
- Experience Documents
- Government Photo ID
- Recent Passport Size Photographs
Candidates may also share their updated resumes through the following email addresses:
Only candidates with relevant experience are encouraged to apply.
