India's DMPLOI - Jobs & Networking AppDr. Reddy’s Laboratories has announced a Career Expo 2026 for experienced professionals in the Injectables Engineering, Manufacturing, Packing, and Utilities functions. This recruitment drive offers an excellent opportunity for candidates with expertise in sterile manufacturing operations, engineering maintenance, utility systems, and injectable packaging to join one of India’s leading pharmaceutical organizations.
The event will be conducted in Hyderabad on 21st June 2026 (Sunday), targeting skilled professionals with experience in USFDA-approved pharmaceutical facilities and strong knowledge of cGMP requirements.
Event Details
Company: Dr. Reddy’s Laboratories Ltd.
Event: Career Expo 2026 – Injectables Engineering & Production
Date: 21st June 2026 (Sunday)
Time: 09:00 AM to 03:00 PM
Venue
Dr. Reddy’s Laboratories Ltd.
Leadership Academy (LA), Bachupally,
Hyderabad – 500090
Work Location
DFL Sterile, Pydibhimavaram, Visakhapatnam
Open Positions
1. Injectable Production / Manufacturing
Experience: 4–8 Years
Qualification:
B.Pharm / M.Pharm
B.Tech / B.E.
Diploma
M.Sc. / B.Sc.
Minimum 60% academic score
Key Skills:
Injectable filling and compounding operations
Autoclave and parts washer handling
Media fill execution
Filling machine qualification
Isolator operation and maintenance
cGMP and GDP compliance
2. Injectable Packing
Experience: 8–10 Years
Qualification:
Diploma / B.Tech / B.E.
Mechanical, Instrumentation, or Electrical disciplines
Minimum 60% academic score
Key Skills:
Auto-cartonator operation
HVLD machine handling
Labeling and serialization systems
Camera inspection systems
Laser coding and case packing
cGMP and GDP documentation
3. Injectable Engineering (Process)
Experience: 5–8 Years
Qualification:
Diploma / B.Tech / B.E.
Mechanical or Instrumentation Engineering
Minimum 60% academic score
Key Skills:
Filling machine maintenance
PFS (Pre-Filled Syringe) machine operation
Troubleshooting and preventive maintenance
CLIT execution as per schedule
Aseptic processing environment experience
4. Injectable Water System & Utilities
Experience: 5–8 Years
Qualification:
Diploma / B.Tech / B.E.
Mechanical or Electrical Engineering
Minimum 60% academic score
Key Skills:
Purified Water (PW) and WFI systems
Pure steam generation
Water treatment and distribution systems
Chillers, compressors, ETP, STP, and nitrogen systems
Preventive maintenance and troubleshooting
Regulatory compliance documentation
Why Join Dr. Reddy’s Laboratories?
Dr. Reddy’s Laboratories is globally recognized for its commitment to innovation, quality, and patient care. Professionals joining the sterile manufacturing division gain exposure to advanced injectable technologies, regulatory-compliant operations, and world-class manufacturing practices.
Key benefits include:
Exposure to global regulatory standards
Career growth in sterile manufacturing
Advanced engineering and production technologies
Opportunity to work in USFDA-approved facilities
Collaborative and innovation-driven work environment
Important Note for Candidates
Candidates should have experience working in USFDA-approved organizations.
Carry updated resumes, educational certificates, experience documents, and recent passport-size photographs.
Candidates are encouraged to register through the official registration link/QR code mentioned in the notification before attending the event.
Technical FAQs
1. What is the purpose of a media fill in injectable manufacturing?
A media fill is a simulation of the aseptic manufacturing process using microbiological growth media instead of product. It validates the sterility assurance of the manufacturing process and operator practices.
2. What is WFI and why is it critical in injectable plants?
WFI (Water for Injection) is highly purified water used in manufacturing sterile pharmaceutical products. It must meet stringent pharmacopeial standards to prevent microbial and endotoxin contamination.
3. What is CLIT in pharmaceutical engineering maintenance?
CLIT (Cleaning, Lubrication, Inspection, and Tightening) is a preventive maintenance methodology used to improve equipment reliability, reduce breakdowns, and ensure consistent production performance.
4. What is HVLD testing in injectable packaging?
HVLD (High Voltage Leak Detection) is a non-destructive container closure integrity testing method used to detect leaks in ampoules, vials, and other sterile packaging formats.
5. Why is GDP important in pharmaceutical manufacturing?
GDP (Good Documentation Practices) ensures that all manufacturing, testing, and maintenance activities are accurately recorded, traceable, and compliant with regulatory requirements, supporting product quality and data integrity.
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