Amneal Hiring QA Validation

Pharma Stuff; Ahmedabad District; On-site; INR 1,500,000 - 2,300,000; Full time

Job summary

Amneal Pharmaceuticals, Inc. in Ahmedabad seeks a senior QA Validation expert for its Injectable manufacturing facility at SEZ Matoda.

The candidate will lead end-to-end validation activities, ensuring GMP compliance and regulatory readiness in a sterile, high‑risk environment. Requirements include M.Pharm/B.Pharm/M.Sc with 8–12 years’ injectable validation experience, hands-on qualification of equipment, HVAC, and utilities, and strong documentation discipline.

Qualifications

• 8 to 12 years of relevant experience in Quality Assurance – Validation.
• Mandatory experience in regulated injectable manufacturing plants.
• Strong knowledge of validation protocols, documentation, and regulatory guidelines.

Responsibilities

• End-to-end validation activities in a regulated injectable manufacturing environment.
• Prepare and review qualification protocols (DQ, IQ, OQ, PQ).
• Execute room mapping and equipment qualification, including HVAC and utilities.
• Ensure GMP compliance and regulatory expectations.

Skills

QA Validation

Regulatory knowledge

Documentation

GMP compliance

Equipment qualification

HVAC qualification

Education

M.Sc, B.Pharm, M.Pharm

Job description

M.Pharm QA Validation Jobs – Amneal Ahmedabad Injectables

Amneal Pharmaceuticals hiring QA Validation roles in Ahmedabad. M.Pharm, B.Pharm, M.Sc eligible. 8–12 years injectable experience.

Amneal Pharmaceuticals, Inc. is hiring experienced Quality Assurance professionals for its Injectable manufacturing facility located at SEZ Matoda, Ahmedabad. This opportunity is targeted at senior‑level candidates with strong exposure to validation activities in regulated injectable plants and hands‑on experience with equipment, utilities, and HVAC qualification.

This role is highly suitable for professionals searching for QA validation jobs in Ahmedabad, injectable pharma quality assurance roles, equipment and utility qualification jobs, and senior QA careers in regulated pharmaceutical manufacturing environments. Amneal offers a global work culture, advanced manufacturing systems, and long‑term career stability within a highly compliant organization.

Company Overview

Amneal Pharmaceuticals, Inc. (NYSE: AMRX) is a global pharmaceutical company with more than 7,500 employees worldwide and a diversified portfolio of over 270 high‑quality medicines. The company is actively involved in the development, manufacturing, and distribution of complex generics, injectables, and specialty pharmaceutical products.

Amneal operates world‑class manufacturing facilities that comply with stringent global regulatory standards. The SEZ Matoda facility in Ahmedabad is a key injectable manufacturing site, supporting regulated market supplies and offering professionals exposure to international compliance, advanced validation systems, and audit‑ready operations.

Job Role & Responsibilities

Quality Assurance – Validation (Injectables)

The selected candidate will be responsible for end‑to‑end validation activities in a regulated injectable manufacturing environment.

Key responsibilities include:

• Equipment qualification including autoclaves, vial washing machines, tunnels, filling machines, UAF, mobile carts, and DPB systems
• HVAC qualification and validation activities
• Utility qualification including PW, WFI, nitrogen, compressed air, and CO2 quantification
• Preparation and review of qualification protocols
• Designing and execution of DQ, IQ, OQ, and PQ protocols
• Room and incubator mapping protocol preparation and execution
• Review of executed qualification reports as per approved protocols
• Ensuring compliance with GMP, validation guidelines, and regulatory expectations

This role plays a critical part in maintaining sterile manufacturing integrity, regulatory compliance, and product quality for injectable medicines.

Eligibility / Qualifications

Educational Qualification

M.Sc, B.Pharm, M.Pharm

Experience Requirement

• 8 to 12 years of relevant experience in Quality Assurance – Validation
• Mandatory experience in regulated injectable manufacturing plants
• Strong knowledge of validation protocols, documentation, and regulatory guidelines

Designation Levels

Senior Executive, Assistant Manager, Deputy Manager

Location & Salary

The job location is SEZ Matoda, Ahmedabad. Salary will be offered as per industry standards and commensurate with qualification, experience, and designation. Final compensation details will be discussed during the interview process.

FAQs

Who can apply for this role?

Experienced QA professionals with injectable validation experience can apply.

Is injectable experience mandatory?

Yes. Experience in regulated injectable manufacturing is mandatory.

What validation areas are covered?

Equipment qualification, utility qualification, HVAC, DQ/IQ/OQ/PQ, and room mapping.

Is this a senior-level role?

Yes. The position is open at Senior Executive to Deputy Manager levels.