Anil Sood
Subject Matter Expert Vaccine Pharmaceutical and Analytical Development (Vpad) @Johnson & Johnson Innovative Medicine
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WORK HISTORY
Subject Matter Expert Vaccine Pharmaceutical and Analytical Development (Vpad) @Johnson & Johnson Innovative Medicine
In this role my responsibilities are to lead deviations, out of specifications and any other quality and manufacturing related issues. To approve the various quality /CMC (Chemistry Manufacturing Control) related memos and other documents as per the requirements for the batch release.• To support the global quality team/Janssen supply chain in the release of vaccines for use.• To lead investigations related to quality and compliance across the manufacturing sites.• To interact with Qualified Person (QP) for queries resolution and Batch release in EMA region.• To participate in the quality related meetings with Janssen quality experts SMEs and EQL for effective resolution of quality incidents.• To lead investigations related to quality and compliance across the manufacturing sites.(ASPEN -South Africa, Catalent -US, CAT- ANAGNI, MERCK-US, GRAM-US, Emergent-US, Bio.E -India and various other External contract labs (EQL network) for COVID 19 vaccine.• To review deviations and quality incidents and approve corrective and preventive actions with site and global quality teams.
EDUCATION
Himachal Pradesh University
Master of Science - MS
Himachal Pradesh University
Bachelor of Science - BS
SKILLS
ABOUT ANIL SOOD
Bio- Pharmaceutical professional with more than 30 years of experience in large scale production and control of vaccines, biologics and sterile injectables with expertise in CMC, Product Development, Quality operations and Technology TransferHighly proficient in handling large teams with multi-location site activities, Contract manufacturing and external quality labs. In depth knowledge of and ability to apply cGMP, USFDA, ANVISA, MHRA and WHO-prequalification regulations and guidelines.Experienced in working with public health organizations and International not-for profit organizations for various activities related to product development, technology transfers, scale-ups and quality operations. Ability to deal and resolve the technical issues for end-to-end delivery and life cycle management of the products.• Expert Panel member of United States Pharmacopeia and Indian Pharmacopeia.• Trainer to WHO fellows from SEARO countries on Production and Quality Control of vaccines and biologics.• Member of AVMI (African Vaccines Manufacturing Initiative)• Trainer to the National Regulators from Drugs Control office and CDSCO (Central Drugs ControlStandards Organisation), New Delhi, India- NRA function• Member of Humane Society International, US
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