Dr. Reddy’s – Walk-In Interview for Manufacturing & Quality Roles on 9th November 2025

Date: Sunday, 9th November 2025
Time: 9:00 AM Onwards
Venue: The Fern Residency, Near Subhash Bridge Corner, RTO Circle, Ahmedabad, Gujarat – 380027
Job Location: Bachupally / Shamirpet, Hyderabad

Dr. Reddy’s is organizing a Career Expo in Ahmedabad to hire professionals for various Manufacturing and Quality roles. Join the event and explore opportunities to work with one of India’s leading pharmaceutical organizations.

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Manufacturing Roles

1. Team Member – Packing

• Expertise in medical device packaging and visual inspection
• Strong documentation skills aligned with cGMP standards

2. TM Engineering – Drug Product / Sterile / Injectable (I&A)

• Hands-on experience in instrumentation & automation
• Automation platforms: Vial Filling, Washing, Tunnel

3. TM Engineering – Drug Substance Mechanical

• Expertise in ABB800xA, Siemens, Allen Bradley PLCs, SCADA systems
• Knowledge of Biopharma equipment (Bioreactors, TFF, ATF)
• Understanding of cGMP & QMS

4. Team Member – Drug Substance (Upstream / Downstream)

• Execution of upstream & downstream unit operations
• Ensuring documentation and GMP compliance

5. Team Member MSAT – Upstream / Downstream

• Expertise in mammalian cell culture, perfusion, and scale-up processes
• Knowledge of Bioreactor characterization, Chromatography, Ultrafiltration, Virus Filtration

Experience: 3–10 Years
Qualification: Diploma / B.Tech / B.Sc / M.Sc / B.Pharm

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Quality Roles

1. Development Quality Assurance

• Involved in DQA for Drug Substance, Drug Product, and Analytical

2. Drug Substance – Quality Assurance

• In-process QA for upstream and downstream manufacturing

3. ASAT – Biosimilar

• Analytical method transfers, investigations, and method validation

4. Quality Control – Bioassay

• Experience in cell-based bioassays, SPR, and FACS techniques

5. Quality Control – RM / PM

• Experience in material analytics, GLP, and analytical techniques

6. Quality Control Associate – Analytical

• Laboratory analysis for biosimilar/biologic products
• Techniques: RP-HPLC, Glycan, SEC, IEX, Peptide Mapping

7. Quality Control – Stability

• Preparation and reporting of stability studies
• Strong understanding of cGMP and documentation practices

8. Quality Control – Lab Support

• Equipment qualification and calibration
• GxP and 21CFR compliance

Experience: 3–10 Years
Qualification: B.Tech / M.Sc / Masters in Biotechnology, Microbiology, or Biochemistry

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Note:
• Immediate joiners are preferred.
• Candidates must carry an updated resume and supporting documents.
• To apply, scan the QR code mentioned in the brochure.