Dr. Reddys Laboratories Walk In 18th Sept 2022 for B.Pharm,M.Pharm

Dr. Reddys Laboratories Walk In 18th Sept 2022 for B.Pharm,M.Pharm. Dr. Reddy€™s Laboratories Ltd (NYSE: RDY) 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. Reddys Laboratories Ltd invites Experienced, Dynamic & Self-Motivated Professionals  for the below positions at the Ahmedabad location. Job Openings for B.Pharm ,M.Pharm Graduates. 

Dr. Reddys Laboratories Ltd is recruiting for the accompanying positions

-MSAT injectables

Refer Notification & all relevant information below. Interested and qualified applicants can attend at scheduled time.

Opportunity subtleties:

Post Name: MSAT injectables

Capability: B.Pharm,M.Pharm

Experienced:03 to 8 years

Set of working responsibilities: Dr. Reddys Laboratories Ltd  Hiring For MSAT injectables !

Significant Details :

Place: Ahmedabad

Walk in Interview Date: 18th September’ 2022

Time: 9.30 AM - 2.00 PM

Walk In Interview Address: Pride Plaza Hotel, Ahmedabad . Judges Bungalow road, SG road, Bodakdev, Ahmedabad 380054, Gujarat, India

Choice Process: The determination will be based on Interview.

Set of working responsibilities:

Reviews and follows safety requirements with respect to process.

Reviews and follows safety requirements with respect to equipment.

Reviews and follows safety requirements in handling materials.

Reviews unit operations, various processes, Process and cleaning validation.

Reviews technical assessments and provide support to execute product trials, CBs & EBs.

Demonstrates basic understanding of regulatory requirements related to technology transfer, cGMP & Sterility strategies.

Reviews process OOS/OOT and defines appropriate CAPAs.

Reviews unit operations, various processes, Process and cleaning validation.

Reviews written procedures (SOPs) & basic GMP requirements.

Reviews procedures related to NPIs/Process validation/Cleaning validation etc.

Understands, follows and executes Good Documentation Practices and ensures contemporaneous entries.

Reviews and provides support for process validation and cleaning validation program.

Reviews and provides technical support to process improvement initiatives.

Reviews and provides technical support in the scaleup of commerical / new products.

Reviews and Provides technical support in evaluating CPPs, CQAs and maintain product robustness throughout product life cycle.

Understands, Review process steps and take the process data from MES/PASX .

Understand business processes with system and can prepare validation documentation.