If you are searching for the latest pharma documentation jobs, Dr. Reddy’s Laboratories recruitment 2026, or B.Pharm jobs in pharmaceutical manufacturing, here’s an excellent opportunity. Dr. Reddy’s Laboratories Ltd. has announced vacancies for the position of Team Member โ Documentation under its Global Manufacturing Organisation (GMO) at Pydibimavaram, Andhra Pradesh.
Candidates with B.Pharm, M.Pharm, or M.Sc qualifications and an interest in pharmaceutical documentation, GMP compliance, manufacturing documentation, SAP, and MES systems are encouraged to apply.
Job Highlights
| Particular | Details |
|---|---|
| Company | Dr. Reddy’s Laboratories Ltd. |
| Position | Team Member โ Documentation |
| Department | Global Manufacturing Organisation (GMO) |
| Location | Pydibimavaram, Andhra Pradesh |
| Qualification | B.Pharm, M.Pharm, M.Sc |
| Experience | As per company requirements |
| Employment Type | Full-Time |
| Industry | Pharmaceutical Manufacturing |
About Dr. Reddy’s Laboratories
Dr. Reddy’s Laboratories is one of India’s leading multinational pharmaceutical companies with operations across 66 countries. Established in 1984, the company employs over 24,000 professionals dedicated to making affordable and innovative medicines accessible worldwide.
The Global Manufacturing Organisation operates world-class manufacturing facilities specializing in APIs, Oral Solid Dosage (OSD), injectables, and other pharmaceutical products while maintaining the highest standards of quality and regulatory compliance.
Key Responsibilities
Selected candidates will be responsible for pharmaceutical manufacturing documentation and GMP compliance activities, including:
- Preparation, review, and approval of Standard Operating Procedures (SOPs).
- Preparation and review of validation protocols and reports.
- Documentation for Confirmatory Batch Protocols.
- Hold Time Protocol preparation.
- Process Evaluation (Pre-validation) Protocol documentation.
- Trial Protocol documentation.
- Process Performance Qualification (PPQ) and Validation Protocols.
- Stability Protocol preparation.
- Preparation of Master Production Records (MPRs).
- Creation of Master Formula Records (MFR).
- Manufacturing Instructions (MI).
- Production Order Raw Materials (PORM).
- Documentation for Oral Solid Dosage (OSD) and Semi-solid manufacturing.
- Design and troubleshooting in MES (PASIX).
- Designing Master Batch Records (MBRs).
- Documentation for PASIX, ESP, GMBR, PVL, and PMBR.
- Cross-functional document circulation and approvals.
- Creation and modification of Bill of Materials (BOM) in SAP.
- Recipe creation in SAP.
- SAP code creation for manufacturing processes.
- Reservation creation in SAP.
- Coordination with cross-functional teams for BOM activities.
Required Qualifications
Applicants should possess:
- B.Pharm
- M.Pharm
- M.Sc
Preferred Skills
- Good Manufacturing Practice (GMP)
- Pharmaceutical documentation
- SOP preparation
- Validation documentation
- Master Production Records
- SAP
- MES (PASIX)
- Batch Record Management
- OSD Manufacturing knowledge
- Semi-solid manufacturing process understanding
Why Join Dr. Reddy’s?
Employees receive industry-leading benefits, including:
- Competitive salary
- Medical insurance for self and family
- Life insurance
- Learning & Development programs
- Career growth opportunities
- Relocation assistance (where applicable)
- Maternity & Paternity benefits
- Modern digital manufacturing environment
- Opportunity to work with global manufacturing teams
Estimated Salary
Based on similar pharmaceutical documentation roles in India, the expected salary may range between:
โน4.5 LPA โ โน7.5 LPA
Actual compensation depends on qualifications, experience, and company policies.
How to Apply
