Amneal Pharmaceuticals is hiring for an Officer, QA Doc Cell position in Ahmedabad, Gujarat. The role is focused on pharmaceutical quality assurance documentation, cGMP compliance, document management, APQR support, deviation and change control activities, and quality-system processes.
This opportunity is relevant for B.Pharm and M.Pharm professionals with at least 1 year of pharmaceutical industry experience who are interested in building their careers in QA documentation and regulated pharmaceutical manufacturing.
Amneal’s official India careers portal currently lists multiple quality and manufacturing opportunities in Ahmedabad, and the company advises candidates to use authorized Amneal recruitment channels and beware of recruitment scams.
Job Details
| Details | Information |
|---|---|
| Company | Amneal Pharmaceuticals |
| Job Title | Officer, QA Doc Cell |
| Department | Quality Assurance |
| Job Function | QA Documentation / Quality Systems |
| Location | Ahmedabad City, Gujarat, India |
| Qualification | B.Pharm / M.Pharm preferred |
| Experience | 1 year or more |
| Industry | Pharmaceutical Manufacturing |
| Job Type | Full-time |
| Salary | Not disclosed by the employer |
About the QA Doc Cell Officer Role
The QA Documentation Cell Officer supports the quality documentation function within a pharmaceutical manufacturing environment. The position involves maintaining documentation systems, supporting regulatory compliance, monitoring quality processes, and helping ensure that manufacturing records and quality documentation meet applicable internal and regulatory requirements.
The role provides exposure to cGMP, pharmaceutical quality systems, APQR, deviations, change control, CAPA, complaints, recalls, and 21 CFR Part 210 and 211.
For professionals beginning or developing a career in pharmaceutical QA, the position can provide practical experience in documentation control and regulated manufacturing quality processes.
Key Responsibilities
The Officer, QA Doc Cell will support activities including:
- Define and maintain quality activities, processes, and documentation standards in accordance with cGMP requirements.
- Support quality documentation infrastructure and systems used within pharmaceutical manufacturing.
- Participate in auditing and monitoring documentation processes against internal procedures and regulatory requirements.
- Maintain efficient workflows, procedures, policies, and inspection programs within the QA documentation cell.
- Support in-process quality monitoring activities and quality-related interactions with vendors.
- Report and assist with troubleshooting manufacturing process deviations and documentation defects.
- Assist in compiling Annual Product Quality Review (APQR) reports.
- Maintain quality documentation in accordance with 21 CFR Part 210 and Part 211 requirements.
- Support change control and deviation management activities under the guidance of senior QA personnel.
- Participate in complaint and recall assessment activities.
- Contribute to the implementation and follow-up of Corrective and Preventive Actions (CAPA).
- Help maintain documentation and records required for pharmaceutical quality and regulatory compliance.
Qualifications and Eligibility
Candidates interested in this Amneal Pharmaceuticals QA job in Ahmedabad should meet the following requirements:
Educational Qualification
- B.Pharm – preferred/eligible
- M.Pharm – preferred
Experience
- Minimum 1 year or more of relevant professional experience.
- Experience in pharmaceutical Quality Assurance, QA Documentation, Document Control, QMS, or manufacturing quality can be relevant to the position.
Useful Technical Knowledge
Candidates may benefit from knowledge of:
- cGMP requirements
- Pharmaceutical QA documentation
- Document control
- SOP management
- APQR/PQR
- Change control
- Deviation management
- CAPA
- Complaint handling
- Recall assessment
- 21 CFR Part 210 and 211
- Pharmaceutical manufacturing documentation
- Internal and regulatory audits
Why This QA Documentation Job May Interest Pharma Professionals
A QA documentation role provides exposure to several important pharmaceutical quality systems rather than focusing only on a single manufacturing activity.
Professionals can develop practical knowledge of:
Documentation Control → GMP Compliance → APQR → Deviations → Change Control → CAPA → Complaints & Recalls → Audit Readiness
Amneal states that its India operations include US FDA-approved facilities and that its careers program provides opportunities across manufacturing, scientific, and other functions. Its careers materials also highlight employee development and opportunities to build new skills and experiences.
Salary and Benefits
The official job description supplied for this vacancy does not disclose a salary or specific role-level benefits.
For SEO purposes, salary estimates should not be presented as employer-confirmed compensation. Google specifically states that baseSalary in JobPosting structured data should represent the actual base salary provided by the employer, rather than an estimate.
Therefore, candidates should confirm the CTC, variable pay, benefits, working hours, and other employment terms directly with Amneal during the recruitment process.
Amneal’s careers information states that the company provides a total-rewards program and emphasizes employee growth and development, although specific benefits can vary by location and role.