Dr. Reddy’s Career Expo in Hyderabad for Injectables (Quality Control)

Updated October 25, 2024
Posted in Degree Jobs / Pharmacy Jobs
Tagged as Dr. Reddy's Career Expo in Hyderabad
2 mins read

Dr. Reddy’s Career Expo in Hyderabad for Injectables (Quality Control)

Dr. Reddy’s Laboratories, a global leader in the pharmaceutical industry, is hosting a Career Expo for professionals experienced in Quality Control for Injectables. This event offers a unique opportunity for candidates to explore exciting roles in Pydbhimavaram, Vishakapatnam at one of India’s premier pharmaceutical companies.

Event Details

Date: 26th October 2024 (Saturday)
Time: 09:00 AM to 03:00 PM
Venue: Dr. Reddy’s Laboratories, Leadership Academy, Bachupally, Hyderabad – 500090

Job Openings: Injectables Quality Control

Work Location

Selected candidates will work at Pydbhimavaram (Vishakapatnam), contributing to the quality control processes for injectables at Dr. Reddy’s.

Department: Quality Control

Job Responsibilities

The Quality Control department plays a crucial role in ensuring that all injectable products meet stringent regulatory and safety standards. Key responsibilities for this position include:

Handling Analytical Instruments: Candidates must have hands-on experience with HPLC (High-Performance Liquid Chromatography) and GC (Gas Chromatography).
Chemical Analysis: Expertise in handling KF Instruments, IR UV, and conducting chemical analyses is required.
Adherence to cGMP Standards: Ensuring compliance with current Good Manufacturing Practices (cGMP), with special emphasis on Good Documentation Practices (GDP).
Stability Knowledge: A solid understanding of stability testing in pharmaceuticals is essential.
Regulatory Experience: Candidates must have experience working in a USFDA-regulated environment and be familiar with regulatory processes.

Required Experience and Skills

Experience: 3 to 8 years of relevant experience in Quality Control for injectables.
Skills:
- HPLC and GC operation expertise.
- Knowledge of KF Instruments, IR UV, and other chemical analysis techniques.
- Practical experience in cGMP environments, with a focus on GDP.
- Familiarity with stability testing and USFDA regulations.