Amneal Pharmaceuticals is hiring for a Quality Assurance (QA) – Validation position at its Oral Solid Dosage (OSD) facility. Candidates with B.Pharm or M.Pharm qualifications and 1–2 years of relevant experience can apply for this pharmaceutical quality assurance job opportunity.
The selected candidate will support process validation, cleaning validation, packaging validation, equipment qualification, documentation, risk assessments, and compliance activities. Local candidates are preferred, and male candidates are preferred as specified in the recruitment announcement.
Amneal Pharmaceuticals QA Validation Job Details
| Job Detail | Information |
|---|---|
| Company | Amneal Pharmaceuticals |
| Job Role | QA – Validation |
| Department | Quality Assurance – Validation |
| Dosage Form | Oral Solid Dosage (OSD) |
| Qualification | B.Pharm / M.Pharm |
| Experience | 1–2 years |
| Job Location | OSD facility, Amneal Pharmaceuticals |
| Candidate Preference | Local candidates preferred; male candidates preferred |
| Salary | Not disclosed |
| Employment Type | Not specified |
| Application Mode | |
| Resume Submission | PriyaR.Sharma@amneal.com |
Note: The exact facility address, salary, and application deadline have not been specified in the recruitment information. Candidates should confirm these details with the recruitment team before proceeding.
Job Responsibilities of QA – Validation
Candidates applying for the Amneal Pharmaceuticals QA Validation vacancy should be familiar with pharmaceutical validation activities, Good Manufacturing Practices (GMP), quality documentation, and cross-functional coordination.
Key responsibilities include:
- Process Validation: Prepare and review process validation protocols and compile process validation reports.
- Cleaning Validation: Prepare and review cleaning validation protocols and reports, and conduct sampling according to approved protocols.
- Packaging Validation: Prepare and review packaging validation protocols and compile validation reports.
- Equipment Qualification: Execute and review qualification, requalification, and validation activities for equipment, systems, facilities, and plant utilities.
- Cross-Functional Coordination: Coordinate with Manufacturing to complete qualification and validation activities on schedule.
- QC and Microbiology Coordination: Work with Quality Control and Microbiology teams on sample preparation and testing for validation and qualification studies.
- Calibration Documentation: Review calibration certificates and reports.
- Risk Assessment: Prepare, review, and execute risk assessments for equipment, processes, facilities, and systems.
- Validation Master Plan: Collect and follow up on data required for the Validation Master Plan (VMP) schedule.
- SOP Management: Prepare and revise Standard Operating Procedures (SOPs) related to QA Validation.
- Change Control and Deviations: Review change controls, planned deviations, and unplanned deviations.
- Additional Duties: Perform other responsibilities assigned by the Head of Department in accordance with departmental instructions.
Eligibility Criteria and Qualifications
Candidates interested in the Amneal Pharmaceuticals QA Validation job should review the following eligibility requirements:
Educational qualification
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
Experience
- 1–2 years of relevant professional experience.
- Experience in pharmaceutical QA, validation documentation, or manufacturing quality systems would be relevant to the listed responsibilities.
Relevant technical knowledge
- Process validation and cleaning validation
- Packaging validation
- Equipment qualification and requalification
- GMP documentation and SOPs
- Change control and deviation management
- Risk assessment and calibration documentation
- Coordination with Manufacturing, Quality Control, and Microbiology teams
The employer has stated a preference for local candidates and male candidates. Applicants should contact the hiring representative if they need clarification about the location or eligibility criteria.
Salary and Benefits
The official recruitment announcement does not specify the salary or employee benefits for this QA Validation position.
Compensation may depend on relevant experience, technical skills, the facility, and the employer’s internal salary structure. Candidates can ask the recruiter about the salary package, employee benefits, shift requirements, and other employment terms during the application process.
This position may be relevant to pharmacy graduates seeking to develop their careers in pharmaceutical quality assurance, validation, GMP compliance, and manufacturing quality systems.
How to Apply for Amneal Pharmaceuticals Recruitment
Eligible candidates can apply by following these steps:
- Prepare an updated resume highlighting your B.Pharm or M.Pharm qualification and relevant QA Validation experience.
- Include experience with process validation, cleaning validation, equipment qualification, validation protocols, reports, SOPs, and GMP documentation, where applicable.
- Mention your current location and availability to join.
- Send your resume to the official email address provided in the recruitment announcement.
Email: PriyaR.Sharma@amneal.com