Amneal Pharmaceuticals Pvt. Ltd. hiring for Quality Assurance (QA) – Validation & QMS
Amneal Pharmaceuticals Pvt. Ltd. is a globally recognized pharmaceutical company committed to delivering high-quality injectable products. As we continue to expand our operations, we are seeking talented and dedicated professionals to join our Quality Assurance (QA) Department at our Injectable Unit, Pipan Plant, Ahmedabad.
If you have experience in QA – Validation or QA – QMS and are looking for a challenging yet rewarding career, this is the perfect opportunity to take your professional journey to the next level.
Why Join Amneal Pharmaceuticals?
At Amneal, we prioritize excellence, innovation, and compliance with global regulatory standards. Our focus is on maintaining the highest levels of quality assurance, validation, and risk assessment to ensure the safety and efficacy of our products. We offer a dynamic work environment, opportunities for professional growth, and a chance to work with industry experts.
Current Openings in Quality Assurance (QA)
We are looking for competent, and motivated candidates for below positions of Quality Assurance (QA) department for Amneal Pharmaceutical Pvt. Ltd (Injectable unit, Pipan Plant, Ahmedabad)
We’re looking for talented individuals to join our team.
Quality Assurance (QA) – Validation & Quality Assurance (QA) – QMS
1) Designation: Executive/ Assistant Manager
Department : Quality Assurance (QA) – Validation
Qualification: B. Pharm / M. Pharm / M. Sc
Total Experience: 05 to 08 years in QA department in sterile/ injectable manufacturing facility.
Job Description:
Ø Execution and review of Qualification / Re-Qualification and Validation activity of Equipment / System / Facility and Plant utilities
Ø Preparation & review of Validation/ Qualification protocol and report
Ø Preparation, review and execution of risk assessment activity related to equipment/ process/ facility/ system
Ø Conduct sampling activity as per the protocols (Process validation and clearing validation etc.)
Ø Assessment of Change Control, Deviation, CAPA, Investigation etc.
2) Designation: Executive/ Assistant Manager
Department : Quality Assurance (QA) – QMS
Qualification: B. Pharm / M. Pharm
Total Experience: 05 to 09 years in QA department in sterile/ injectable manufacturing facility.
Job Description:
Ø Review of Change controls, CAPAs, Unplanned Deviations, Planned Deviations, Risk Assessment.
Ø Review of Out of Specification, Out of Alert limit, Computer system incident, Environmental Excursions.
Ø Performing investigation of Unplanned deviations, Out of specification, Out of Alert Limit, Computer system incident.
Ø Tracking and closure of Change controls, CAPAs, Unplanned Deviations, Planned Deviations, Risk Assessment, Out of Specification, Out of Alert limit, Computer system incident.
Ø Performing investigation of Market Complaints.
Candidate with good communication & interpersonal skills and understanding of regulatory requirement will be preferred.
Interested candidates can share their CV on [email protected] by mentioning the subject line “Application for QA -Validation/ QA-QMS Department” or they can refer other suitable candidates for this job opportunity.
Shape Your Future with Amneal Pharmaceuticals!
This is your chance to be a part of a leading pharmaceutical organization where quality, innovation, and professional growth go hand in hand. Join us and make a meaningful impact in the field of Quality Assurance.
Disclaimer:
Beware of fake job offers claiming to be from Amneal Pharmaceuticals Pvt. Ltd. or Companies under Amneal Group (collectively referred to as “AMNEAL”). Amneal neither send job offers from free email services like Gmail, Rediffmail, Yahoo mail, Hotmail, etc. nor charges any fees/security deposit from any job seekers. Amneal will not be responsible to anyone acting on an employment offer not directly made by Amneal. Stay vigilant and report any suspicious activity to Amneal.
