Pharm'Up 
Amneal Pharmaceuticals, a global leader with a portfolio of over 270 high-quality medicines, is currently hiring experienced professionals for its Quality Control (Oral Solid Dosage) department. This role is specifically focused on QMS Investigation, requiring a blend of technical expertise and high-level documentation skills.
Vacancy Overview
| Feature | Details |
| Role | QMS – Investigation (Quality Control) |
| Department | Quality Control (Oral Solid Dosage – OSD) |
| Qualification | B.Sc / M.Sc / M.Pharm |
| Experience | 2 to 8 Years |
| Job Location | SEZ Matoda, Ahmedabad |
Core Responsibilities
The candidate will be responsible for ensuring the compliance and integrity of the quality systems at a regulated OSD manufacturing plant.
- Investigations: Lead and document thorough investigations related to quality deviations and laboratory operations.
- Analytical Writing: Draft, review, and refine high-quality technical reports, official communications, and audit-ready presentations.
- Compliance: Ensure all documentation is grammatically precise and professional to withstand scrutiny from global regulatory bodies (FDA, MHRA, etc.).
- Cross-Functional Collaboration: Coordinate with various departments to maintain accurate records of findings and follow-up actions.
- Audit Support: Provide well-structured documentation to support internal and external quality audits.
Key Skills Required
- Strong Documentation: Exceptional command of analytical writing and spoken English.
- Technical Knowledge: Proven experience in quality systems (OOS, OOT, Deviations) within a regulated environment.
- Attention to Detail: Ability to create professional reports that are “audit-ready.”
How to Apply
Interested and eligible candidates are encouraged to share their updated CV via email:
Email: chandanid@amneal.com
Last Date to Apply: February 10, 2026
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