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PHARMA JOBS POST > Manufacturing > Dr. Reddy’s Walk-In Interview | Packing, Engineering, Manufacturing, QC | 23rd March 2025
ManufacturingPackingQuality Control

Dr. Reddy’s Walk-In Interview | Packing, Engineering, Manufacturing, QC | 23rd March 2025

ARPITA
Last updated: March 8, 2025 11:25 am
ARPITA 2 years ago
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Dr. Reddy’s Laboratories is a global pharmaceutical company headquartered in Hyderabad, India. Founded in 1984, the company develops, manufactures, and markets a wide range of pharmaceutical products, including generic medicines, active pharmaceutical ingredients (APIs), and biosimilars. Dr. Reddy’s operates in multiple therapeutic areas, such as oncology, gastroenterology, dermatology, and cardiovascular diseases.

Requirement Details:

1)Team Member – Packing

Skills Required:
• Expertise in qualification for device packing and
Cartridge line – Auto Cartonator would be advantage.
• Should have Experience in Leak Detecting Machine, Pouch Packing and Case Packer

• Education: Diploma/B-Tech (Mechanical, Instrumentation, Electrical) (Minimum 60%)
• Experience: 3 – 8 Years

2) Team Member – Manufacturing

Skills Required:

  • Expertise in Handling Filling operations of PFS, Cartridges
  • Complex Injectable compounding / Peptide Compounding
  • Exposure to Isolators, Vial Wash, Tunnel, Lyophilizer, and Autoclave
  • Must have experience with USDA regulatory environment.
  • Should have Aspectic operations.
  • Education: Diploma / B-Tech – Engineering (Minimum 60%)
  • Experience: 3 – 8 Years

3)Team Member – Engineering

• Skills Required:
• Utility, Water systems, Instrumentation, Process control.
• Must have exposure in handling of Process Area maintenance like Manufacturing Vessels, Filling machine, Autoclave, Isolators and Lyophilization.

• Education: Diploma / B.Tech / (Mechanical, Electrical,
Electronics & Instrumentation) – (Minimum 60%)
• Experience: 3 – 8 Years

4)Team Member – Quality Control

Skills Required:
• Hands on experience in Handling of HPLC, GC.
• Expertise in Handling of KF instrument. IR UV & Chemical Analysis
• Working experience in a GMP with a special emphasis on
GDP(Good Documentation Practices)
• Knowledge on Stability.
• Must have experience with USFDA regulatory environment and process.

•Education: M.Sc. (Minimum 60%)
•Experience: 3 – 8 Years

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