
Jay Jariwala
Jay Jariwala is an ex-FDA regulator, and currently a Regulatory Compliance Senior Director at Sidley Austin LLP, a... | Silver Spring, Maryland, United States
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Jay Jariwala’s Emails ja****@fd****.gov
Jay Jariwala’s Phone Numbers No phone number available.
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Jay Jariwala’s Location Silver Spring, Maryland, United States
Jay Jariwala’s Expertise Jay Jariwala is an ex-FDA regulator, and currently a Regulatory Compliance Senior Director at Sidley Austin LLP, a global law firm with a leading Food, Drug and Medical Device (FDMD) practice. He has more than 15 years of experience in the life sciences industry and regulatory compliance, including a diplomatic overseas assignment as Assistant Country Director (Drugs-India) for the US FDA. As an ex-FDA regulator, he has a unique insight into the expectations and challenges of government agencies such as the FDA, EMA, European Commission, and NMPA. He uses his expertise in drug CGMP, regulatory inspections, manufacturing, and compliance to advise major drug, biopharmaceutical, biotechnology, and medical device companies on complex regulatory and enforcement issues, and to devise sophisticated engagement strategies that protect their interests and advance their goals. He is passionate about ensuring the availability of quality drugs in the market place, and resolving complex compliance, enforcement, regulatory, and policy issues in a heavily scrutinized environment. He has received multiple honors and awards from the FDA and other organizations for his leadership, dedication, and commitment in the regulatory compliance field.
Jay Jariwala’s Current Industry Sidley Austin
Jay
Jariwala’s Prior Industry
Office Of Compliance Center For Devices And Radiological Health Us Fda
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Office Of Manufacturing Quality Office Of Compliance Cder Us Fda
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Office Of Global Policy And Strategy Office Of The Commissioner Us Fda
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Fda
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Sidley Austin
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Work Experience

Sidley Austin
Senior Director, Regulatory Compliance
Mon Aug 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Fda
Team Leader / Combination Products SME, Office of Manufacturing Quality, OC, CDER, US FDA
Sun Mar 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Aug 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)
Office Of Global Policy And Strategy Office Of The Commissioner Us Fda
Assistant Country Director (Drugs-India), Office of Global Operations, US FDA (Overseas Assignment)
Sat Sep 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Mar 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time)
Office Of Manufacturing Quality Office Of Compliance Cder Us Fda
Combination Product Subject Matter Expert, Office of Compliance, CDER
Sat Nov 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Sep 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Office Of Manufacturing Quality Office Of Compliance Cder Us Fda
Team Leader / Combination Products SME, Office of Manufacturing Quality, OC, CDER, US FDA
Sat Nov 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Sep 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Office Of Compliance Center For Devices And Radiological Health Us Fda
Medical Device Single Audit Program (MDSAP) Team Member (on Detail), Office of Compliance, CDRH
Wed Jan 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Nov 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Office Of Compliance Center For Devices And Radiological Health Us Fda
Quality System Specialist, Office of Compliance, Center for Devices and Radiological Health (CDRH),
Thu Nov 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Jan 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Office Of Compliance Center For Devices And Radiological Health Us Fda
Compliance Officer, Office of Compliance, Center for Devices and Radiological Health (CDRH), US FDA
Fri Aug 01 2008 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Nov 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)