Dr.Reddy’s-Interviews for Freshers & Experienced on 24th Mar’ 2024

Dr.Reddy’s-Interviews for Freshers & Experienced on 24th Mar’ 2024

Dr.Reddy’s-Interviews

Dr. Reddy’s Laboratories is an Indian multinational pharmaceutical company located in Hyderabad, Telangana, India. The company was founded by Kallam Anji Reddy, who previously worked in the mentor institute Indian Drugs and Pharmaceuticals Limited.

Quality Control Department
Experience : 2- 8 Years
Qualification : MSc, BSc (Minimum 60%)
Skills : • Experience in QC analysis of RM, PM, FP & stability. Hands on experience in handling of instruments HPLC, GC, UPLC, Dissolution, UV-vis spectrophotometer, FTIR, KF etc. 

IPQA Department
Experience : 4- 8 Years
Qualification : MSc Microbiology / B.Pharma – Engg (Minimum 60%)    
Skills : Responsible to Injectable line clearance, material verification,start-up checks and in-process checks as per the batch manufacturing record, and Batch Packing record.

Injectables Production / Manufacturing Department
Experience : 2- 8 Years
Qualification : Diploma / B-Tech – Engg (Minimum 60%)

Skills : • Expertise in Handling Filling operations of PFS, Catriage B+S Liquid Vial / Compounding / Aseptic 
• Exposure to Isolators, Vial Wash, Tunnel, Lyophilizer, and Autoclave
• Must have experience with USFDA regulatory environment and process.

Work Location : Duvvada / Pydibhimavaram – Vishakhapatnam

Candidate should have exposure working in USFDA Approved organizations Preferred candidate from Injectables and Quality Control.

Walk in Interview
Date : 24th March 2024
Time : 09:30 Hrs. to 15:00 Hrs.
Venue – Ginger Gajuwaka, 27- 8-308/1/1, Near Vadlapudi, Sri Ramnagar, Sri Nagar, Railway 

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Job Category: pharma
Job Type: Full Time
Job Location: Vishakhapatnam

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Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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