Dr. Reddy’s Laboratories, a leading global pharmaceutical company, is hosting an exciting Career Expo in Hyderabad on September 7, 2025, at their Leadership Academy in Bachupally, Telangana. This is a prime opportunity for skilled professionals to join their Oral Solid Dosage (OSD) Engineering and Manufacturing teams in Pydibhimavaram, Andhra Pradesh. With a focus on innovation and quality, Dr. Reddy’s seeks candidates with expertise in process maintenance, water systems, mechanical maintenance, production, packing, and quality control (QC). If you’re passionate about advancing pharmaceutical manufacturing and have experience in USFDA-regulated environments, this is your chance to contribute to the mission of “Good Health Can’t Wait.”
Job Responsibilities
- Process Maintenance & Instrumentation:
- Maintain and troubleshoot plant process and manufacturing equipment.
- Calibrate equipment and work with PLC programming/SCADA systems.
- Plan and execute Preventive Maintenance Programs (PMP).
- Water System Operations:
- Operate and maintain water systems, including Water for Injection (WFI) and pure steam generation.
- Ensure compliance with regulatory guidelines for purified water in OSD manufacturing.
- Perform sanitization, sterilization, and passivation of water systems.
- Mechanical Maintenance:
- Oversee maintenance of OSD equipment, including primary and secondary packaging lines.
- Execute preventive maintenance, root cause analysis (RCA), and breakdown resolution.
- Maintain documentation like SPM checklists and SAP records.
- Production & Packing (Derma):
- Manage tube filling, jar filling, and bottle filling for ointments, creams, and lotions.
- Ensure adherence to CGMP practices and regulatory standards.
- Quality Control (QC) Analyst:
- Test raw materials, finished products, and stability samples.
- Ensure compliance with 21 CFR and other regulatory requirements.
Qualifications
- Educational Requirements:
- Process Maintenance/Instrumentation/Water System: Diploma/B.Tech in Electrical, Instrumentation, or Electronics.
- Mechanical Maintenance: Diploma/B.Tech in Mechanical Engineering.
- Production & Packing (Derma): Diploma/B.Tech/B.Pharm.
- QC Analyst (RM & Stability): B.Sc/M.Sc.
- Minimum 60% academic score throughout.
- Experience: 3-7 years in pharmaceutical manufacturing, preferably in USFDA-approved organizations.
- Skills:
- Expertise in plant process equipment, packaging lines, and water system maintenance.
- Knowledge of PLC programming, SCADA systems, P&ID, and regulatory guidelines.
- Proficiency in CGMP, 21 CFR compliance, and audit management.
- Strong troubleshooting, communication, and documentation skills.
- Familiarity with TPM concepts, SAP, and RCA for preventive maintenance.
Benefits of Joining Dr. Reddy’s
- Career Growth: Opportunities to work with cutting-edge OSD manufacturing technologies.
- Global Impact: Contribute to Dr. Reddy’s mission of delivering affordable, high-quality medicines worldwide.
- Collaborative Environment: Join a team of passionate professionals in a USFDA-compliant setting.
- Professional Development: Access to training and development programs at Dr. Reddy’s Leadership Academy.
How to Apply
Interested candidates should register by scanning the QR code provided in the official Dr. Reddy’s Career Expo announcement or visit Pharmabharat.com for details. The event is scheduled for Sunday, September 7, 2025, from 9:00 AM to 3:00 PM at:
Venue:
Dr. Reddy’s Laboratories Ltd. (Leadership Academy)
Survey No. 47, Bachupally Village, Bachupally, Malkajgiri, Telangana 500090
Bring your resume, academic certificates, and relevant documents. Walk-in interviews will be conducted, and shortlisted candidates will be contacted for further steps.
FAQs
Q: What roles are available at the Dr. Reddy’s Career Expo?
A: Roles include Team Member Engineering (Process Maintenance, Instrumentation, Water System), Mechanical Maintenance, Production & Packing (Derma), and QC Analyst (RM & Stability).
Q: What is the experience level required for these positions?
A: Candidates need 3-7 years of experience in pharmaceutical manufacturing, ideally in USFDA-approved facilities.
