이 직무에 대한 지원은 더 이상 접수되지 않습니다.
- Support the audit delivery in the medical device sector (ISO 13485, MDD/MDR CE Marking)
- Assist in obtaining and maintaining relevant approvals and accreditations
- Develop procedures that satisfy appropriate requirements
- Help define criteria for the control and development of Competences Centres
- Provide product support to the network and coordinate projects related to product development
- Promote existing products and services within the organisation
- Provide training on technical requirements and details MDR requirements
- Meet clients, competitors, and stakeholders regularly to understand their needs and anticipate evolutions
- Cooperate on defining and implementing global marketing initiatives
- Bachelor's degree or above in a related discipline
- 7-10 years related work experience in medical device audit
- Excellent writing and verbal communication and presentation skills
Medical Device Auditor - 서울시, 대한민국. - Robert Walters
설명
A global testing and certification services provider is looking for a Medical Device Auditor. The chosen applicant will be developing procedures that meet accreditation requirements while also providing valuable product support.
Responsibilities:
Requirements:
About the Company:
A global leader in testing, inspection, and certification services. The company has established itself as a trusted partner for businesses seeking to enhance their performance, reduce risks, and ensure compliance with industry standards.
Keywords:
인증, 시험, 의료기기, 지원, 기술, 국제
2032610/001