This opportunity is suitable for pharmaceutical professionals with experience in Quality Management Systems (QMS), deviation handling, CAPA, change control, GMP compliance, and manufacturing quality processes.
Professionals looking to advance their career in biologics manufacturing and pharmaceutical quality operations can explore this opportunity.
Job Overview
| Particulars | Details |
|---|---|
| Position | Team Member – Drug Product – QMS |
| Company | Dr.Reddy’s |
| Location | Hyderabad, Telangana |
| Job Type | Full-Time |
| Experience | 4 - 8 years |
| Category / Department | Pharma |
| Application Mode | Online |
🏢 About Dr.Reddy’s
Dr. Reddy’s Laboratories is a global pharmaceutical organization focused on delivering affordable and innovative healthcare solutions.
The company works across multiple therapeutic areas with expertise in generic medicines, biosimilars, and advanced pharmaceutical manufacturing.
Dr. Reddy’s Biologics division focuses on developing and manufacturing high-quality biosimilar products while following global regulatory and quality standards.
📝 Job Description
Dr. Reddy’s Laboratories Hiring | Team Member – Drug Product – QMS | Pharma Jobs
🏢 Company: Dr. Reddy’s Laboratories Limited
💼 Position: Team Member – Drug Product – QMS
📍 Location: Hyderabad, Telangana
🏭 Department: Manufacturing – Biologics
⏳ Experience: 4–8 Years
🎓 Qualification: B.Pharm / M.Pharm / Pharmaceutical Sciences / Chemistry / Related Life Sciences
📌 Employment Type: Full-Time
🏢 Work Mode: On-Premise
📩 Application Mode: Online Application
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Job Overview
Position: Team Member – Drug Product (QMS)
Department: Manufacturing – Biologics
Job Family: Production – Biosimilar (Drug Product)
Location: Hyderabad, Telangana
Experience: 4–8 Years
Employment Type: Full-Time
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Required Qualifications
🎓 Candidates should possess:
• Bachelor’s Degree in Pharmaceutical Sciences
• Master’s Degree in Pharmaceutical Sciences
• Chemistry
• Related Life Science disciplines
Experience:
• 4–8 years of pharmaceutical industry experience in QMS and quality operations.
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Employee Benefits
Dr. Reddy’s offers:
✔ Competitive compensation package
✔ Career growth opportunities
✔ Learning and development programs
✔ Medical insurance benefits
✔ Life insurance coverage
✔ Maternity & paternity benefits
✔ Relocation support (where applicable)
✔ Professional development opportunities
✔ Inclusive and collaborative workplace culture
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Salary Details
Estimated salary range:
💰 ₹8.5 LPA – ₹13.5 LPA (CTC)
Actual compensation may vary based on experience, skills, and interview performance.
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Why Join Dr. Reddy’s?
✔ Opportunity to work with a leading global pharmaceutical company.
✔ Exposure to biologics manufacturing and biosimilar products.
✔ Work on global quality standards and regulatory processes.
✔ Strong career growth opportunities in pharmaceutical quality.
✔ Innovation-driven and employee-focused work environment.
🎯 Key Responsibilities
- ✓ Selected candidates will be responsible for:
- ✓ Managing Quality Management System activities for Drug Product Manufacturing.
- ✓ Handling deviations, manufacturing investigations, CAPA implementation, and change controls.
- ✓ Reviewing and updating Batch Production Records (BPR), Master Formula Records (MFR), SOPs, and quality documents.
- ✓ Ensuring timely closure of deviations and CAPA actions.
- ✓ Supporting QMS documentation and compliance activities.
- ✓ Ensuring adherence to FDA, EMA, ICH, ISO, and GMP requirements.
- ✓ Conducting internal audits and self-inspection activities.
- ✓ Supporting regulatory inspections and customer audits.
- ✓ Coordinating quality-related training programs.
- ✓ Participating in risk assessments and continuous improvement initiatives.
- ✓ Collaborating with QA, QC, Production, Regulatory, and other cross-functional teams.
💡 Required Qualifications & Skills
Frequently Asked Questions
Q1. What position is Dr. Reddy’s hiring for?
Dr. Reddy’s is hiring for Team Member – Drug Product (QMS).
Q2. What experience is required for this role?
Candidates should have 4–8 years of experience in pharmaceutical quality management systems.
Q3. Which qualifications are eligible?
B.Pharm, M.Pharm, Pharmaceutical Sciences, Chemistry, or related Life Science qualifications are eligible.
Q4. What department is this role for?
The position is part of Manufacturing – Biologics (Drug Product).
Q5. Where is the job location?
The role is based in Hyderabad, Telangana.
Q6. What skills are preferred?
Experience in QMS, CAPA, deviations, change control, GMP compliance, audits, and documentation management is preferred.