Ninoo Grover
Commercial Quality Lead - India Consumer Health
- Role
- Associate Director - Business Quality, India J & J Consumer at Johnson & Johnson
- Location
- Mumbai, MH, IN
- LinkedIn followers
- 500 followers
About Ninoo Grover
Career SummaryAnalytical and quality-oriented professional with an eye for detail, offering nearly 33 years of a successful career with diverse roles, with proven results in spearheading the entire gamut of Quality Management functions across Medical / Pharma / Consumer Lifecycle Success in implementing various standards to improve the product quality & services, establishing KPIs, monitoring & measuring performance followed by evaluating and improving continually. Effectively managed QA programs such as CAPA, Deviation Management, Computer System Validation, Internal Auditing, Change Controls, Customer Complaints, Vendor Management, and Regulatory Inspections.Established QMS formalized procedures, trained, oriented, mentored & guided teams to achieve both organization and quality goals & objectives. Contributed immensely to Global Strategic Initiatives with key focus on organizational vision & goal.
Experience
Associate Director - Business Quality, India J & J Consumer
Nov 2015 — Present · Johnson & Johnson Consumer, IN
Quality oversight and responsibility for Consumer business in India, ensuring quality and compliance during the entire life cycle of the commercialized product- Lead robust implementation and review of the Quality Management system for India Consumer business- Ensure ongoing compliance of all J&J Consumer products marketed in India domestic market as well as cluster markets (viz, Sri Lanka & Bangladesh)- Partner with cross functional technical teams to ensure compliance of NPDs with local regulations and continuing compliance of actual products with regulatory commitments and dossiers and subsequent regulatory changes- Continuously monitor and improve quality systems & procedures to ensure full compliance to Quality Policy & Standards- Ensure appropriate risk assessment and management for products - Ensure implementation of end-to-end complaint vigilance process. Lead the periodic review of complaints & adverse events with the appropriate local and regional stakeholders as defined in the QMS and track actions identified to address adverse trends- Lead preparedness of Local Company for Audits and assessments- Ensure budget management, staffing, career planning & development and providing a safe working environment for the team.
Education
MSc
Master of Science, Microbiology, General
1988 — 1990
Skills
- Biotechnology
- Gmp
- Process Improvement
- Medical Devices
- Capa
- Validation
- Healthcare
- Quality System
- Quality Systems
- Pharmaceutical Industry
- Sop
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