Date: November 3, 2024 (Sunday)
Time: 09:00 AM to 03:00 PM
Venue: Dr. Reddy’s Laboratories, Leadership Academy, Bachupally, Hyderabad- 500090
About Dr. Reddy’s Laboratories: Dr. Reddy’s Laboratories, founded in 1984 and headquartered in Hyderabad, is a leading Indian multinational pharmaceutical company. We focus on the research, development, manufacturing, and marketing of a diverse range of pharmaceutical products, including APIs, generics, biosimilars, and OTC medications. We are committed to providing affordable, innovative medicines globally and prioritize sustainability and corporate social responsibility.
Departments Hiring:
1. Injectables – Manufacturing
- Experience: 2-6 Years
- Qualification: Diploma/B-Tech (Minimum 60%)
- Skills Required:
- Expertise in handling filling operations of PFS, Cartridges, and B+S Liquid Vial/Compounding/Aseptic.
- Exposure to Isolators, Vial Wash, Tunnel, Lyophilizer, and Autoclave.
- Experience with the USFDA regulatory environment.
2. Engineering
- Experience: 4-8 Years
- Qualification: Diploma/B.Tech (Mechanical/Instrumentation) (Minimum 60%)
- Skills Required:
- Experience in process area maintenance (Manufacturing Vessels, Filling machine, Autoclave, Isolators, Lyophilization).
- Automation Engineering experience in manufacturing and filling areas.
- Mandatory: Electrical 33KV license.
- Knowledge of HVAC, Utility, Water systems, Instrumentation, Process control.
3. Quality Control (Microbiology)
- Experience: 4-8 Years
- Qualification: M.Sc. in Microbiology (Minimum 60%)
- Skills Required:
- Responsible for sampling & analysis of water samples and preparation of reports.
- Maintenance of microbiological reference cultures and compliance with GLP.
- Preparation of laboratory reagents, disinfectants, indicators, and volumetric solutions.
- Experience in BET, MLT, and sterility testing.
4. Quality Control
- Experience: 3-8 Years
- Qualification: M.Sc. (Minimum 60%)
- Skills Required:
- Hands-on experience with HPLC, GC, and KF instruments.
- Expertise in IR, UV & Chemical Analysis.
- Experience in cGMP with a focus on Good Documentation Practices (GDP).
- Knowledge of stability studies and experience with USFDA regulatory processes.
How to Apply:
Interested candidates should register by scanning the QR code below.
