Dr.Reddy’s Laboratories Ltd is an integrated global pharmaceutical company, committed to providing affordable and innovative medicines for healthier lives. Through its three businesses – Pharmaceutical Services and Active Ingredients, Global Generics and Proprietary Products Dr.Reddy™s offers a portfolio of products and services including APIs, custom pharmaceutical services, generics, biosimilars and differentiated formulations.
We are excited to share a fantastic opportunity at Dr. Reddy’s Laboratories. We are on the lookout for passionate, talented individuals who thrive in dynamic environments and are eager to make an impact in the pharmaceutical industry. If you’re someone who excels in these areas, we invite you to explore our open positions and take the next step in your career with us. Join our innovative and driven team today.
Great Opportunity! Come join us at 🌟Dr.Reddy’s Laboratories – Injectables, Visakhapatnam🌟
Hiring For QC-Micro / Packing Department
- Department: QC-Microbiology / Packing
- Experience: 3-8 years of experience
- Qualification: M.Sc Micro / Diploma
- Designation: Team Member
- Job Location: VIZAG
How to Apply:
- Please Share Resume/curriculum vitae Mail Id : saikrishnakota@drreddysfl.com
Work location – Pydibheemavaram
DFL-02 (Dr. Reddy’s Formulations Limited)
Injectable Facility
Skills Required for QC-Micro:
- Environmental Monitoring (Active & Passive air sampling)
- Water Sampling and Water testing.
- MLT Testing and WFI BET.
- Finished product and Raw material Sampling.
- Microbiological Assay by cup plate method.
- Sterility testing and sterility tube observation.
- Media preparation and media fill activity.
- Online documentation as per GMP.
- Have a knowledge on pharma regulatory audits
Skills Required for Packing:
- Handling of High Voltage Leak Detection Machine, Laser Jet Printing.
- Expertise in Handling of Cartonators (Make:CAM)
- Shipper label Printer
- Working experience in a cGMP with a special emphasis on GDP(Good Documentation Practices)
- Knowledge on Handling of Word & Excel.
- Must have experience with EUGMP regulatory environment and process.
