עוגן מדטק השמה

Do you currently live in Israel?

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What is your level of proficiency in Hebrew?

What is your level of proficiency in English?

Do you currently reside in the geographic area between Rehovot and Haifa?

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Do you have a valid driver's license?

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Are you able and willing to travel daily between client sites located between Rehovot and Haifa?

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How many years of experience do you have in Quality Assurance (QA) for medical devices?

How many years of experience do you have in Regulatory Affairs (RA) for medical devices?

How many years of combined experience do you have in medical device Quality Assurance and/or Regulatory Affairs?

Have you led QA/RA projects for medical devices that successfully achieved major regulatory milestones (such as FDA submission, CE marking, ISO 13485 certification, or QMS establishment)?

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Do you have hands-on experience preparing and submitting FDA and CE regulatory submissions for medical devices?

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Have you managed multidisciplinary teams and had full project ownership (including delivery, timelines, and coordination) for QA/RA projects in the medical device industry?

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Do you have practical experience with core QMS activities (such as CAPA, nonconformances, change control, audits, complaints, training, and document control) in the medical device industry?

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Do you have client-facing or consulting experience in the medical device industry?

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Do you have an engineering degree?

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קורות חיים (PDF) *

הגשת מועמדות — Senior Project Manager for QA/RA Medical Device Consulting Company