drjobs Team Lead Auditing MDR/IVDR

Team Lead Auditing MDR/IVDR

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1 Vacancy
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Job Location drjobs

Hamburg - Germany

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Description

We are looking for aTeam Lead Auditing MDR/IVDR to joinDNV MEDCERT in Hamburg Germany. The Team Lead will manage a team of Auditors and Experts enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. The role is essential to lead and develop the Audit group and to enable organizational growth in the IVDR sector.

  • Leadingthe Audit team (Auditors and Experts) to ensure complete accurate and timely Audit and Technical Documentation Assessments.
  • Responsible for the development of the IVDR business implementation of the business strategy as well as recruitment development and support of additional resources within this area.
  • Establishing and developingclose internal collaboration with the IVDR team of DNV Product Assurance AS.
  • Management of teams to improve efficiency increase customer satisfaction and ensure compliance with standards.
  • Conduct assessmentsin accordance with MDR 2017/745 or IVDR 2017/746.
  • Conduct audits under EN ISO 13485MDR 2017/745 or IVDR 2017/746 and MDSAP.
  • Responsible for reporting to Head of Auditing and Experts.


Responsibilities
  • A competitive compensation and benefit package
  • DNV training and qualification program
  • A professional community in a prestigious technological company
  • Possibilities to work with interesting and challenging projects
  • Access to an extensive competence network

DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender religion race national or ethnic origin cultural background social group disability sexual orientation gender identity marital status age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity.





Qualifications
  • An academic degree in Medical Technology Engineering or Natural Science.
  • 5 years work experience in the regulatory environment of ISO 13485 MDR IVDR or MDSAP.
  • Excellent knowledge and understanding of the Medical Device industry preferably with experience covering both Notified Bodys and Industry / Manufacturing / Pharmaceutical companies.
  • Ability to represent the company by participating in internal audits with accreditation bodies.
  • Ability to use analytical data in order to monitor and drive performance excellence.
  • Excellent communication presentation and leadership skills; ability to interpret and present highly complex and strategically significant information.
  • We hire for mindset! Forward-thinking mindset and an understanding of the Notified Body environment.
  • A pragmatic working style: Understanding the big picture while being able to dive into the detail.
  • Written and verbal communication skills; fluent in German and English.

Please note that we cannot proceed to the interview stage without the following documents: Curriculum Vitae (CV); Cover- /Motivation Letter; University Diplomas & Transcripts; Reference Letter(s). All documents shall preferably be submitted in English. Please provide them at your earliest convenience to ensure a smooth and timely assessment process. Your cooperation in this matter is greatly appreciated.







Employment Type

Full Time

Company Industry

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