5.00(4)

Career in Pharma Industry: Quality Control by Sunil Singh

Description

Around 50 percent of the total workforce of Pharmaceutical Industry works in Quality & Production departments. While production is responsible for getting the drug ready, Quality department plays a significant role in keeping a strong check over the quality of pharmaceutical products. If you are looking for a career in Quality Control Department of Pharma Industry, just go through this brief course. You will get a good perspective about Quality Control in Pharma & it will also help you to make a better decision for your career.

Language: Hinglish (Hindi+English)

If you need Career Counselling Sessions for making a great career decision for Pharmaceutical Industry Click HERE

Also Explore: Career in Quality Assurance & Career in Core Pharma Manufacturing

Topics for this course

1 Lessons05m 19s

Career in Quality Control | Pharmaceutical Industry

Counselling Session for Quality Control Department5:19

About the instructor

Sunil Singh has given 25 years of his life perfecting the art of upholding the highest possible standards of medicine quality. Graduating with M.Sc. in Organic Chemistry in 1994 from Banaras Hindu University (BHU), he has discharged numerous responsibilities during his career like handling of regulatory and customer audits, people development through training and demonstration, implementation and monitoring of Quality Systems based on FDA’s six quality systems approach, preparation of corporate guidelines for implementation across other sites in the organisation, monitoring the stability of API and DF, monitoring of Quality Systems through Quality Metrics as per new FDA/ MHRA guidelines and improving the productivity of QC labs by streamlining processes and removing bottlenecks in the system. He has been instrumental in the implementation of GMP/ Quality systems in compliance with guidelines/regulations like Schedule M, ICH Q7, USFDA, MCA, TGA, ANVISA, MCC, WHO, 21 CFR Part 210 & 211 etc. Handling of change control, Product complaints, response to regulatory audits, batch recall, CAPA, investigation, deviation management from set parameters/ regulations, OOS and Risk management. He has audited more than 75 plants that handle Drug Formulation, API, Intermediate and Packaging Material manufacturing. He has also handled Third Party manufacturing sites and ensuring timely batch release while making sure the required regulations are met. He has also effectively handled more than 50 inspections by reputed customers and regulatory agencies like USFDA, TGA, MCC, WHO, ANVISA, IMB, Ministry of Health (Russia) successfully. His core skills include Training and Development based on cGMP guidelines and regulations, Audit and compliance, Mentoring and Quality management system design and their effective implementation. Unflinching in resolve and surprisingly simple and logical in approach. He has started his career with Lupin and worked with organisations like Matrix Laboratories, Mylan Pharmaceuticals, Aurobindo Pharma, Ranbaxy, Sun Pharma, Dabur Pharma, Dr. Reddy’s Laboratories and Jubilant Generics.
5.00 (38 ratings)

14 Courses

1863 students

Student Feedback

5.0

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A good course for the beginners.

Useful

Great one

Useful course