Amneal Pharmaceuticals is Hiring for Quality Control & QMS Roles

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.

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 – 382220,
Gujarat, India

Job Locations:

Industry: Pharmaceutical Manufacturing (OSD Regulated Plant)

Important Note: No vacancies are available in the Microbiology section.

1. Quality Control (Topical)

Designation

Qualification

Experience

2. Quality Control

Designation

Qualification

Experience

3. Quality Control (QMS – Investigation)

Designation

Qualification

Experience

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.

Candidates should possess any of the following qualifications:

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

• Quality Control (Topical): 1–5 Years
• Quality Control: 1–5 Years
• QMS Investigation: 7–12 Years

Note: Relevant experience in an OSD regulated pharmaceutical plant is required.

Selected candidates can expect:

• Estimated Salary: ₹3.5 LPA – ₹12 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.

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.