Nicholas Werner Email and Phone Number
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Experienced regulatory affairs professional with a diverse experience in the medical device and life sciences industries. I began my career serving as a Premarket Reviewer and a Postmarket Analyst with the US Food and Drug Administration before transitioning to working on total product lifecycle regulatory affairs for one of the largest medical device manufacturers in the country. I have additionally provided a broad range of services to clients, including documentation/system assessments and remediation, regulatory submission preparation and review, and regulatory strategy. My unique background allows me to approach regulatory issues from the perspectives of both industry and health authorities.
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Director Of Regulatory Affairs, Portfolio ComplianceCoopervision May 2023 - PresentSan Ramon, California, Us -
Director Of Regulatory AffairsChronomics May 2022 - Feb 2023London, United Kingdom, Gb -
Senior Principal Consultant, Regulatory AffairsSuttons Creek, Inc. May 2021 - May 2022Westlake Village, California, Us -
Director, Regulatory Policy & EducationNetwork Partners Jul 2019 - May 2021
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Senior Scientific Advisor - Regulatory AffairsNetwork Partners May 2018 - Jul 2019
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Senior Staff Regulatory Affairs SpecialistStryker Mar 2017 - May 2018Kalamazoo, Mi, Us -
Staff Regulatory Affairs SpecialistStryker Jan 2015 - Feb 2017Kalamazoo, Mi, Us -
Biomedical EngineerFda May 2008 - Dec 2014Silver Spring, Md, UsBiomedical Engineer / Scientific Reviewer – Office of Device Evaluation (ODE), Dental Devices Branch and General Hospital Devices BranchBiomedical Engineer / Analyst – Office of Surveillance and Biometrics (OSB), Product Evaluation BranchMy work in the Office of Device evaluation required me to participate in the interpretation and review of scientific data to ensure the safety and effectiveness of medical devices. This position allowed me to use my own judgment to gather and assess pertinent data and make recommendations on medical device actions [e.g., 510(k), PMA, and IDE decisions]. Proper time management and the ability to communicate effectively with various industrial professionals were greatly utilized in this position.My work in the Office of Surveillance and Biometrics required me to utilize an internal Oracle-based program, the Manufacturer and User Facility Device Experience (MAUDE) Database, for the evaluation, analysis, and investigation of medical device problem reports. From these reports, it was my responsibility to detect short term device problems along with potential trends that had been occurring over a longer period of time. This position provided the responsibility to initiate investigations of medical devices that warranted such action. Leadership skills were also utilized in this position, as many investigative actions require a presentation with a thorough background and potential steps forward addressed. Composing Adverse Event Report Memos required a detailed knowledge of various types of devices and how their design and/or intended use could contribute to a reported event. This work also required me to discuss policies on reporting with industry and to provide additional information regarding medical device reporting regulations as necessary.
Nicholas Werner Skills
Nicholas Werner Education Details
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University Of PittsburghBioengineering And Biomedical Engineering
Frequently Asked Questions about Nicholas Werner
What company does Nicholas Werner work for?
Nicholas Werner works for Coopervision
What is Nicholas Werner's role at the current company?
Nicholas Werner's current role is Director of Regulatory Affairs at CooperVision.
What is Nicholas Werner's email address?
Nicholas Werner's email address is ho****@****ail.com
What is Nicholas Werner's direct phone number?
Nicholas Werner's direct phone number is +120252*****
What schools did Nicholas Werner attend?
Nicholas Werner attended University Of Pittsburgh.
What skills is Nicholas Werner known for?
Nicholas Werner has skills like Regulatory Affairs, Fda, Biomedical Engineering, Medical Devices, Capa, R&d, Data Analysis, U.s. Food And Drug Administration, Regulatory Submissions, Biotechnology, Life Sciences, Adverse Event Reporting.
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