QA Jobs in Pharma: Amneal Pharmaceuticals is Hiring a Senior Executive/Assistant Manager – Apply Now
Are you a Graduate in pharmacy looking for QA Jobs in Pharma? Amneal Pharmaceuticals is hiring a Senior Executive/Assistant Manager – QMS (Market Complaints) in Ahmedabad, Gujarat. This role is ideal for professionals with B.Pharm or M.Pharm qualifications and expertise in market complaint investigations, CAPA implementation, and global regulatory compliance. The position offers an opportunity to lead root cause analysis, data integrity assessments, and cross-functional coordination to ensure product quality and regulatory adherence.
About the Company:
Amneal Pharmaceuticals is a leading global pharmaceutical company dedicated to developing and delivering high-quality, affordable medicines across multiple therapeutic areas. Headquartered in the United States, with significant operations in India, Amneal combines scientific innovation, regulatory expertise, and operational excellence to serve patients worldwide. The company emphasizes diversity, equity, and inclusion, fostering a workplace where every employee can thrive. Amneal invests in research and development, state-of-the-art manufacturing, and quality systems to ensure compliance with global standards, including cGMP and regulatory guidelines. With a strong presence in formulation development, generic and specialty pharmaceuticals, Amneal continues to expand its portfolio and reach, providing medicines that improve health outcomes while maintaining affordability.
Job Details:
- Job Title: Senior Executive / Assistant Manager – QMS (Market Complaints)
- Location: Ahmedabad, Gujarat, India
- Job Category: Quality Assurance
- Job Schedule: Full-Time
- Apply Before: 10/14/2025
Job Responsibilities:
- Handle market complaint investigations and ensure timely closure.
- Coordinate with cross-functional teams including Production, QC, Packaging, and Regulatory Affairs for data collection and assessment.
- Perform investigations to identify root causes of complaints, including product quality, packaging, labeling, or distribution issues.
- Evaluate batch manufacturing records, deviations, OOS/OOT results, change controls, and other relevant documents.
- Prepare comprehensive investigation reports with scientific justification.
- Recommend and track CAPA implementation to prevent recurrence of issues.
- Communicate outcomes to stakeholders and regulatory bodies as required.
- Support trending analysis and periodic review of complaint data for improvement opportunities.
- Ensure compliance with global regulatory expectations (USFDA, EMA, MHRA, WHO) and internal quality policies.
- Monitor CAPA status and effectiveness, participate in effectiveness reviews, and identify continuous improvement areas.
Education:
B.Pharm / M.Pharm
Skills & Qualifications:
- Analytical & problem-solving skills: Advanced
- Managing multiple investigations & CAPAs: Advanced
- Knowledge of cGMP, GDP & ICH Q10: Advanced
- Global regulatory compliance knowledge: Advanced
- Automated QMS platform proficiency: Advanced
- Root cause analysis & investigation: Advanced
- Data integrity (ALCOA+) knowledge: Advanced
