Vice President Global Quality Assurance and Regulatory Affairs
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Gedved
Vice President Global Quality Assurance and Regulatory Affairs
Do you want to create possibilities with ergonomic assistive devices and patient handling equipment?
https://uhc.dk/wp-content/uploads/2020/10/Videoannoncen.mp4
As VP Global QA/RA at ETAC Group you will play a key role in driving the global quality and regulatory agenda in the organization and ensuring group compliance. The Etac Group has strong growth ambitions globally, and solid compliance and quality resources and processes are a high priority.
With direct report to Etac’s CEO & Group President you are a part of the Group Management Team and you will work closely with all Business Units. You are responsible for strengthening the Quality and Regulatory function globally while also ensuring a close link between the Quality and Regulatory function and the Manufacturing, Product Development and Marketing departments.
Your success depends on your ability to work closely with and support and coach the QA/RA teams in Denmark, Sweden, Poland and the US.
A selection of your tasks are:
Your qualifications are well documented within the field of QA/RA in relation to medical devices. You have a background from working with Quality Management in manufacturing companies that work with both product development and new product introduction. Furthermore, international working experience will be an advantage.
You have a Graduate degree within Engineering, Business, Healthcare or other related fields. A Postgraduate degree is considered an additional merit.
You are a person with a positive attitude and a collaborative working style. With your good communication skills you facilitate and encourage teamwork in the QA/RA teams and in the coorporation across business functions.
Etac Group offers great opportunities for personal development and the possibility of contributing to the development of Etac on a group level.
Travelling: Travelling to sites in Sweden, Poland and the US.
Domicile: Gedved, Denmark
For more details about the job or the company, please contact CEO Jørn Duhn, Unique Human Capital on M: +45 21 75 19 25 or Senior Research Consultant Stine W. Kristiansen, Unique Human Capital on M: +45 51 72 89 43. All applications must be in English and are treated confidentially.
Do you want to create possibilities with ergonomic assistive devices and patient handling equipment?
https://uhc.dk/wp-content/uploads/2020/10/Videoannoncen.mp4
As VP Global QA/RA at ETAC Group you will play a key role in driving the global quality and regulatory agenda in the organization and ensuring group compliance. The Etac Group has strong growth ambitions globally, and solid compliance and quality resources and processes are a high priority.
With direct report to Etac’s CEO & Group President you are a part of the Group Management Team and you will work closely with all Business Units. You are responsible for strengthening the Quality and Regulatory function globally while also ensuring a close link between the Quality and Regulatory function and the Manufacturing, Product Development and Marketing departments.
Your success depends on your ability to work closely with and support and coach the QA/RA teams in Denmark, Sweden, Poland and the US.
A selection of your tasks are:
- Coordinating, reviewing and updating e.g. registrations, policies, processes and ensuring compliance at a group level
- Maintaining, developing and streamlining e.g. the Quality Management Systems, Quality processes and tools
- Being a trusted advisor for marketing, production and product development regarding QA/RA compliance in the global product portfolio. The products are Class 1 medical devices
- Preparing and managing audits in coorporation with site QA/RA responsible persons
Your qualifications are well documented within the field of QA/RA in relation to medical devices. You have a background from working with Quality Management in manufacturing companies that work with both product development and new product introduction. Furthermore, international working experience will be an advantage.
You have a Graduate degree within Engineering, Business, Healthcare or other related fields. A Postgraduate degree is considered an additional merit.
You are a person with a positive attitude and a collaborative working style. With your good communication skills you facilitate and encourage teamwork in the QA/RA teams and in the coorporation across business functions.
Etac Group offers great opportunities for personal development and the possibility of contributing to the development of Etac on a group level.
Travelling: Travelling to sites in Sweden, Poland and the US.
Domicile: Gedved, Denmark
For more details about the job or the company, please contact CEO Jørn Duhn, Unique Human Capital on M: +45 21 75 19 25 or Senior Research Consultant Stine W. Kristiansen, Unique Human Capital on M: +45 51 72 89 43. All applications must be in English and are treated confidentially.
Information og data
Denne ledige stilling har jobtypen "Direktør", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Gedved.
Jobbet er oprettet på vores service den 23.10.2020, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Direktør
- Gedved
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