Sharon Resnick Email & Phone Number | 👍More than 18 years' of experience in medical device quality & regulatory compliance. 📄Established and upgraded numerous effective Quality Management Systems that comply with the regs. 🎯Supported end-to-end projects from product concept to regulatory submissions. 👩🏻‍🏫Drives true organizational excellence while providing guidance, training, leadership and engaging employees. ✅ISO 13485:2016 Lead Auditor: internal audits, supplier audits, MDSAP audits, MDR audits, gap assessments and due dilligence 👩🏻‍💼Retained services in QA/RA department(s). 🫱🏼‍🫲🏻Training and mentoring junior staff. 🗃️Regulatory submissions qualityworks. was founded in 2020 to provide quality and regulatory solutions to medical device companies from concept to market. Need more details? ✔️send me an email to: sharon@qualityworks.pro ✔️visit my website: www.qualityworks.pro ✔️call me at: +972-53-531-5259

Sharon Resnick

👍More than 18 years' of experience in medical device quality & regulatory compliance. 📄Established...
Israel

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Sharon Resnick’s Email sharon@qualityworks.pro

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Sharon Resnick’s Location Israel

Sharon Resnick’s Current Industry Qualityworks

Sharon Resnick’s Prior Industry Beammed | Physio Logic | Tel Aviv University | Philips | Cdp Medical

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Owner, QA/RA Expert

2020-10-01 00:00:00 - Present

Director of Quality Assurance and Regulatory Affairs

2019-09-01 00:00:00 - 2021-08-01 00:00:00

Executive Program Manager, QA/RA Expert, Management Member

2014-03-01 00:00:00 - 2019-08-01 00:00:00

Visiting Lecturer

2018-12-01 00:00:00 - 2019-08-01 00:00:00

Senior Quality & Regulatory Manager

2010-09-01 00:00:00 - 2014-03-01 00:00:00

Quality & Regulatory Manager

2005-02-01 00:00:00 - 2010-09-01 00:00:00

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Sharon Resnick is a 👍More than 18 years' of experience in medical device quality & regulatory compliance. 📄Established and upgraded numerous effective Quality Management Systems that comply with the regs. 🎯Supported end-to-end projects from product concept to regulatory submissions. 👩🏻‍🏫Drives true organizational excellence while providing guidance, training, leadership and engaging employees. ✅ISO 13485:2016 Lead Auditor: internal audits, supplier audits, MDSAP audits, MDR audits, gap assessments and due dilligence 👩🏻‍💼Retained services in QA/RA department(s). 🫱🏼‍🫲🏻Training and mentoring junior staff. 🗃️Regulatory submissions qualityworks. was founded in 2020 to provide quality and regulatory solutions to medical device companies from concept to market. Need more details? ✔️send me an email to: sharon@qualityworks.pro ✔️visit my website: www.qualityworks.pro ✔️call me at: +972-53-531-5259