B Pharm Job Opportunity at Amneal | Manufacturing Documentation Role | Apply Now
Looking for a B Pharm Job in the pharmaceutical manufacturing industry? Amneal Pharmaceuticals is hiring an Officer – Manufacturing Documentation at its Hyderabad facility. This opportunity allows pharmacy graduates to build expertise in quality documentation, deviation investigations, CAPA management, risk assessment, audit support, and cGMP compliance while working in a regulated pharmaceutical manufacturing environment. Candidates seeking a career in pharmaceutical quality systems, compliance, and manufacturing operations can explore this exciting opportunity with Amneal.
- Job Title: Officer – Manufacturing Documentation
- Job Location: Hyderabad, Telangana, India
About the Company
Amneal Pharmaceuticals is a global pharmaceutical company engaged in the development, manufacturing, and distribution of high-quality generic and specialty medicines. With a strong focus on quality, compliance, and innovation, Amneal offers rewarding career opportunities for pharmacy professionals across manufacturing, quality, regulatory, and research functions.
Job Description
Amneal is hiring an Officer – Manufacturing Documentation for its Hyderabad facility. This pharma job is ideal for B. Pharm graduates interested in Quality Management Systems (QMS), manufacturing documentation, deviation investigations, CAPA management, risk assessment, SOP preparation, audit support, and cGMP compliance within a regulated pharmaceutical manufacturing environment.
B Pharm Job – Key Responsibilities
- Manage Change Controls, Deviations, and Quality Management System (QMS) documents.
- Prepare and review SOPs, protocols, BMRs, and BPRs.
- Ensure timely CAPA implementation and closure.
- Conduct deviation, OOS, and non-conformance investigations.
- Perform root cause analysis and risk assessments.
- Implement mitigation plans through Quality Risk Management (QRM).
- Conduct internal audits and support regulatory inspections.
- Participate in customer and regulatory audits.
- Evaluate and investigate market complaints.
- Provide training on quality processes and procedures.
- Coordinate with cross-functional teams for compliance activities.
- Complete assigned SOP training and documentation updates.
Eligibility Criteria- For B Pharm Job
- Education: B. Pharm
Required Skills
- QMS, cGMP & CAPA Management
- Change Control & Compliance Processes
- Risk Assessment & Root Cause Analysis
- Deviation Management
- SOP Review & Manufacturing Documentation
- Analytical Thinking & Problem Solving
- Cross-Functional Coordination
- Communication & Attention to Detail
