Pierre Bounaud
Diligent and responsible Regulatory Affairs professional, and PhD-educated chemist, with a proven ability to drive regulatory projects to... | San Diego County, California, United States
Pierre Bounaud’s Emails pb****@ac****.com
Pierre Bounaud’s Phone Numbers No phone number available.
Social Media
Pierre Bounaud’s Location San Diego County, California, United States
Pierre Bounaud’s Expertise Diligent and responsible Regulatory Affairs professional, and PhD-educated chemist, with a proven ability to drive regulatory projects to completion. A self-motivated and organized team member with good problem-solving skills, attention to details, and effective time management skills. A clear communicator who can work with people of different backgrounds in a team-based environment. Specific expertise in medical device regulatory submissions with the FDA. CORE COMPETENCIES • 510(k) submissions, pre-submissions, RFDs • Technical File & Design Dossier preparation • Project planning and management • Problem solving and strategic thinking • Knowledge of FDA US and EU regulations • Knowledge of ISO 13485, ISO 14971, IEC 62366 • Analytical & Organic Chemistry • Drug Discovery & Development • Bilingual (French)
Pierre Bounaud’s Current Industry Rqm
Pierre
Bounaud’s Prior Industry
The Scripps Research Institute
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Lg Biomedical Institute
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Sgx Pharmaceuticals
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Pb Consulting
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Ardea Biosciences
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Selexagen
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Zenobia Therapeutics
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Djo Global
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Bsn Medical
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Cerus Endovascular
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Acknowledge Regulatory Strategies
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Rqm
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Work Experience
Rqm
Principal Consultant
Wed Dec 01 2021 05:30:00 GMT+0530 (India Standard Time) — Present
Acknowledge Regulatory Strategies
Principal Consultant
Wed Mar 01 2017 05:30:00 GMT+0530 (India Standard Time) — Mon Nov 01 2021 05:30:00 GMT+0530 (India Standard Time)
Cerus Endovascular
Regulatory Affairs Consultant
Sat Oct 01 2016 05:30:00 GMT+0530 (India Standard Time) — Thu Dec 01 2016 05:30:00 GMT+0530 (India Standard Time)
Bsn Medical
Regulatory Affairs Consultant
Fri Jul 01 2016 05:30:00 GMT+0530 (India Standard Time) — Sat Oct 01 2016 05:30:00 GMT+0530 (India Standard Time)
Djo Global
Regulatory Affairs Consultant
Sat Feb 01 2014 05:30:00 GMT+0530 (India Standard Time) — Mon Jun 01 2015 05:30:00 GMT+0530 (India Standard Time)
Zenobia Therapeutics
Director of Chemistry
Wed Jun 01 2011 05:30:00 GMT+0530 (India Standard Time) — Wed May 01 2013 05:30:00 GMT+0530 (India Standard Time)
Selexagen
Medicinal Chemistry consultant
Mon Feb 01 2010 05:30:00 GMT+0530 (India Standard Time) — Sat Oct 01 2011 05:30:00 GMT+0530 (India Standard Time)
Ardea Biosciences
Medicinal Chemistry Consultant
Tue Sep 01 2009 05:30:00 GMT+0530 (India Standard Time) — Wed Sep 01 2010 05:30:00 GMT+0530 (India Standard Time)
Pb Consulting
Founder
Thu Jan 01 2009 05:30:00 GMT+0530 (India Standard Time) — Wed Mar 01 2017 05:30:00 GMT+0530 (India Standard Time)
Sgx Pharmaceuticals
Senior Scientist II
Sat Dec 01 2001 05:30:00 GMT+0530 (India Standard Time) — Wed Oct 01 2008 05:30:00 GMT+0530 (India Standard Time)
Lg Biomedical Institute
Scientist
Sun Oct 01 2000 05:30:00 GMT+0530 (India Standard Time) — Mon Oct 01 2001 05:30:00 GMT+0530 (India Standard Time)
The Scripps Research Institute
Post-doctoral scientist
Tue Sep 01 1998 05:30:00 GMT+0530 (India Standard Time) — Fri Sep 01 2000 05:30:00 GMT+0530 (India Standard Time)Skills
Languages
Pierre Bounaud Email Addresses
FAQ About Pierre Bounaud
-
Pierre Bounaud is located at
San Diego County, California, United States -
Pierre Bounaud is a
Diligent and responsible Regulatory Affairs professional, and PhD-educated chemist, with a proven ability to drive regulatory projects to completion. A self-motivated and organized team member with good problem-solving skills, attention to details, and effective time management skills. A clear communicator who can work with people of different backgrounds in a team-based environment. Specific expertise in medical device regulatory submissions with the FDA. CORE COMPETENCIES • 510(k) submissions, pre-submissions, RFDs • Technical File & Design Dossier preparation • Project planning and management • Problem solving and strategic thinking • Knowledge of FDA US and EU regulations • Knowledge of ISO 13485, ISO 14971, IEC 62366 • Analytical & Organic Chemistry • Drug Discovery & Development • Bilingual (French) Rqm -
Pierre Bounaud currently works in the
Rqm -
Pierre Bounaud specializes in
Diligent and responsible Regulatory Affairs professional, and PhD-educated chemist, with a proven ability to drive regulatory projects to completion. A self-motivated and organized team member with good problem-solving skills, attention to details, and effective time management skills. A clear communicator who can work with people of different backgrounds in a team-based environment. Specific expertise in medical device regulatory submissions with the FDA. CORE COMPETENCIES • 510(k) submissions, pre-submissions, RFDs • Technical File & Design Dossier preparation • Project planning and management • Problem solving and strategic thinking • Knowledge of FDA US and EU regulations • Knowledge of ISO 13485, ISO 14971, IEC 62366 • Analytical & Organic Chemistry • Drug Discovery & Development • Bilingual (French) -
Pierre Bounaud speaks the following languages:
No languages available. -
Pierre Bounaud has prior experience in the following industries:
Acknowledge Regulatory Strategies , Cerus Endovascular , Bsn Medical , Djo Global , Zenobia Therapeutics , Selexagen , Ardea Biosciences , Pb Consulting , Sgx Pharmaceuticals , Lg Biomedical Institute , The Scripps Research Institute -
Pierre Bounaud has the following professional experience:
Rqm , Acknowledge Regulatory Strategies , Cerus Endovascular , Bsn Medical , Djo Global , Zenobia Therapeutics , Selexagen , Ardea Biosciences , Pb Consulting , Sgx Pharmaceuticals , Lg Biomedical Institute , The Scripps Research Institute . -
You can view Pierre Bounaud’s
LinkedIn profile at LinkedIn URL. -
Pierre Bounaud’s work email addresses are
[email protected] . -
Pierre Bounaud works at
Rqm
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