Dr. Reddy’s Career Expo – Team Member Roles in Manufacturing & Quality on 9th Nov

Explore pharma jobs in Hyderabad at Dr. Reddy’s Career Expo. Walk-in interview for manufacturing and QA/QC jobs with 3-10 years of experience. Kickstart your pharmaceutical careers in India—attend on Nov 9!

About the Company

Dr. Reddy’s Laboratories Ltd., established in 1984, is a premier global pharmaceutical powerhouse headquartered in Hyderabad, India. Renowned for its innovation in generics, biosimilars, and differentiated formulations, the company prioritizes patient-centric solutions and regulatory excellence.

With USFDA, EMA, and WHO approvals, Dr. Reddy’s operates in over 100 countries, driving growth through R&D investments exceeding $100 million annually. Its commitment to cGMP compliance and sustainable practices makes it a top choice for pharmaceutical careers in India, fostering talent in cutting-edge biopharma environments.

Job Details

• Company Name: Dr. Reddy’s Laboratories Ltd.
• Experience: 3 to 10 Years
• Qualification: Diploma/B.Tech/B.Sc/M.Sc/B.Pharm/B.Tech or Masters in Biotechnology/Microbiology/Biochemistry
• Location: Bachupally / Shamirpet, Hyderabad
• Work Type: On-site

Job Description

Dr. Reddy’s is hosting a dynamic Career Expo to recruit passionate professionals for manufacturing and quality roles, emphasizing innovation in drug substance, drug product, and biologics.

These positions demand expertise in GMP compliance and advanced biopharma processes, offering a gateway to impactful pharma jobs. With a focus on upstream/downstream operations and analytical excellence, join a team accelerating “Good Health Can’t Wait.”

Team Member – Packing

• Department: Manufacturing
• Role: Medical device packaging and visual inspection with cGMP alignment
• Experience: 3 to 10 Years
• Education/Qualification: Diploma/B.Tech/B.Sc/M.Sc/B.Pharm

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

• Department: Manufacturing
• Role: Instrumentation & Automation for vial filling, washing, and tunnel systems
• Experience: 3 to 10 Years
• Education/Qualification: Diploma/B.Tech/B.Sc/M.Sc/B.Pharm

TM Engineering – Drug Substance Mechanical

• Department: Manufacturing
• Role: Automation platforms including ABB800xA, Siemens, Allen Bradley PLCs, SCADA, and biopharma equipment like bioreactors and TFF
• Experience: 3 to 10 Years
• Education/Qualification: Diploma/B.Tech/B.Sc/M.Sc/B.Pharm

Team Member – Drug Substance Upstream / Downstream

• Department: Manufacturing
• Role: Execute upstream/downstream unit operations with GMP documentation and compliance
• Experience: 3 to 10 Years
• Education/Qualification: Diploma/B.Tech/B.Sc/M.Sc/B.Pharm

Team Member MSAT – Upstream / Downstream

• Department: Manufacturing
• Role: Specialist in mammalian cell culture, perfusion, scale-up, single-use tech, bioreactor characterization, chromatography, ultrafiltration, and virus filtration
• Experience: 3 to 10 Years
• Education/Qualification: Diploma/B.Tech/B.Sc/M.Sc/B.Pharm

Development Quality Assurance

• Department: Quality
• Role: QA in drug substance, drug product, and analytical development
• Experience: 3 to 10 Years
• Education/Qualification: B.Tech or Masters in Biotechnology/Microbiology/Biochemistry

Quality Control – Bioassay

• Department: Quality
• Role: Cell-based bioassays, SPR, and FACS techniques
• Experience: 3 to 10 Years
• Education/Qualification: B.Tech or Masters in Biotechnology/Microbiology/Biochemistry

Drug Substance – Quality Assurance

• Department: Quality
• Role: In-process QA for drug substance manufacturing, upstream, and downstream
• Experience: 3 to 10 Years
• Education/Qualification: B.Tech or Masters in Biotechnology/Microbiology/Biochemistry

Quality Control – RM/PM

• Department: Quality
• Role: Material analytics lab with GLP adherence and safety practices; sample analysis via analytical techniques
• Experience: 3 to 10 Years
• Education/Qualification: B.Tech or Masters in Biotechnology/Microbiology/Biochemistry

ASAT – Biosimilar

• Department: Quality
• Role: Analytical method transfers, validation, real-time investigations, annual performance, and query resolution
• Experience: 3 to 10 Years
• Education/Qualification: B.Tech or Masters in Biotechnology/Microbiology/Biochemistry

Quality Control – Lab Support

• Department: Quality
• Role: Equipment qualification, calibration, periodic GxP reviews per GAMP5 and 21CFR
• Experience: 3 to 10 Years
• Education/Qualification: B.Tech or Masters in Biotechnology/Microbiology/Biochemistry

Quality Control Associate Analytical

• Department: Quality
• Role: Lab analysis for biosimilars/biologics using RP-HPLC, Glycan, SEC, IEX, PepMap
• Experience: 3 to 10 Years
• Education/Qualification: B.Tech or Masters in Biotechnology/Microbiology/Biochemistry

Quality Control – Stability

• Department: Quality
• Role: Stability study protocols/reports, batch planning, chamber maintenance per cGMP
• Experience: 3 to 10 Years
• Education/Qualification: B.Tech or Masters in Biotechnology/Microbiology/Biochemistry

Skills/Qualifications

• Expertise in cGMP, GLP, GAMP5, and 21CFR compliance
• Proficiency in biopharma equipment like bioreactors, TFF, ATF, and automation platforms (ABB, Siemens, Allen Bradley)
• Hands-on experience in upstream/downstream operations, cell culture, chromatography, and ultrafiltration
• Strong analytical skills in HPLC, bioassays, SPR, FACS, and stability studies
• Knowledge of documentation, strategic planning, and safety practices
• Preferred regulatory exposure including ICH guidelines and QMS

Key Responsibilities

• Execute unit operations and inspections
• Validate methods and troubleshoot processes
• Maintain equipment and perform calibrations
• Document compliance and investigate deviations
• Analyze samples using advanced techniques
• Support scale-up and stability studies
• Ensure GMP and regulatory adherence

Benefits/Perks

• Accelerated career growth in biosimilars and generics
• Extensive training in cutting-edge biopharma tech
• Competitive salary with performance bonuses
• Inclusive work culture promoting innovation
• Global exposure via international collaborations

How to Apply

Attend the Career Expo to apply directly—scan the QR code at the venue for instant registration. Bring your resume and qualifications. For additional pharma jobs, visit Pharma Recruiter. Seize this chance for QA jobs and manufacturing roles in pharmaceutical careers in India—register today!

Walk-in Interview Details

• Date: 9th November 2025 (Sunday)
• Time: 9:00 AM Onwards
• Venue: The Fern Residency, Near Subhash Bridge Corner, RTO Circle, Ahmedabad, Gujarat 380027
• Contact/Email: Scan QR at venue or visit Dr. Reddy’s careers page

Why You Should Join

Dr. Reddy’s cultivates a vibrant culture of recognition, where your expertise in QC jobs and production fuels breakthroughs in affordable healthcare. Benefit from unmatched career stability in a $3B+ revenue giant, with personalized growth paths and leadership programs. Immerse in a compliant yet innovative ecosystem, advancing biosimilars and sterile injectables for global impact.

FAQs