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
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Team Member – Drug Product – QMS role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹3,80,000 - ₹7,00,000 per annum (Mid-level QC/chemist). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
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.
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