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    Rishi Mtopra

    Senior Regulatory Affairs Specialist

    Rishi Mtopra is an experienced Senior Regulatory Affairs Specialist with a strong background in the IVD and medical device sector.

    Known as the 'Registration Guru' among colleagues at Thermo RA for their ability to manage multiple registrations simultaneously, handle MDSAP Audits, utilize Registration Spreadsheets, complete Project Management courses, and mentor junior staff.

    Recognized as a fantastic team player who excels in challenging environments, adept at bringing a calm and methodical approach to Regulatory Affairs, drawing from taekwondo training.

    Committed to staying updated with the latest guidance and best practices to ensure team alignment and optimal performance, aiming to leave a lasting legacy in the IVD medical device sector similar to Usain Bolt.

    Education includes a Post Graduate Diploma in Regulatory Affairs, Pharmacy Administration, and Pharmacy Policy and Regulatory Affairs from Raaj Global Pharma Regulatory Affairs Consultants, an MSc in Drug Discovery & Development from the University of Sunderland, and a Master of Pharmacy from the University of Sunderland.

    Worked as a Senior Regulatory Affairs Specialist at Thermo Fisher Scientific and held positions at various prestigious organizations like STRATEC Biomedical AG, Zimmer Biomet, Epistem Ltd., Sinclair IS Pharma PLC, PPD, Reckitt Benckiser, Lloydspharmacy, among others.

    Rishi Mtopra invites inquiries for guidance on medical devices and IVD medical devices, emphasizing safety and expertise in these areas.

    Rishi Mtopra
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    Location

    United Kingdom