M Pharm Jobs in Ahmedabad: Amneal Pharmaceuticals is seeking an Experienced Asst/Deputy Manager – Apply Now
Are you passionately looking for M Pharm Jobs in Ahmedabad? Amneal Pharmaceuticals is seeking an experienced Asst/Deputy Manager – Formulation & Development (Injectable) in Ahmedabad, Gujarat. This role offers exposure to product development of injectable dosage forms for regulated markets, including liquid solutions, lyophilized products, suspensions, and drug-device combinations. Candidates will work closely with cross-functional teams, ensuring Quality by Design (QbD) implementation, regulatory compliance, and successful scale-up of formulations.
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: Asst/Deputy Manager – Formulation & Development (Injectable)
- Location: Ahmedabad, Gujarat, India
- Job Category: Formulation R&D
- Job Schedule: Full-time
- Apply Before: 10/18/2025
Job Responsibilities:
- Lead product development activities for injectable dosage forms, including general injectables, onco, and peptide products.
- Understand ANDA and 505b2 product filings and prepare regulatory documentation.
- Handle various dosage forms: liquid solution, lyophilized, suspension, and drug-device combination products.
- Prepare and review product development reports, MFR, stability protocols, SOPs, and other study documents.
- Implement Quality by Design (QbD) principles, including QTTP, CQA, CPP, CMA, risk assessment, and control strategy.
- Coordinate with regulatory affairs, manufacturing, QA/QC, warehouse, and engineering for scale-up and exhibit batches.
- Manage QMS documents, including change controls, planned/unplanned deviations.
- Review API, excipients, in-process, finished product, and shelf-life specifications for injectable products.
- Prepare and review necessary ANDA submission documents and respond to regulatory queries.
Education:
Experience in injectable product development and regulatory compliance for regulated markets.
