Regulatory Affairs Professional - Maternity Cover

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Are you looking for independence in your job, variance and a working day characterized by exciting new challenges? Would you like to be part of a great team in [xxxxx]’s Corporate Regulatory Affairs department and ensure that we meet regulatory requirements?

Then [xxxxx] might be your next career move.

Our purpose is ‘together, we rethink solutions to save life and improve patient care’

Our aspiration is to be the most customer-centric company in our field and to expand our leading position within single use endoscopy solutions. Our four strategic focus areas are: Providing innovative solutions for true customer needs, to excel in execution across the value chain, take leaps towards a sustainable future, bring people together in one shared culture. In addition, [xxxxx] is one of the first companies to be fully compliant with the new EU Medical Device Regulation (MDR).

To be able to meet the increasing regulatory requirements on time, [xxxxx] is looking for a candidate to join our Regulatory Innovation team for Visualization. You will be part of a highly skilled team of 5 people, and you will report to Head of Regulatory Affairs, Visualization & Vigilance, Kristine Rasmussen.

Executing efficiently

As part of an organization with short lines of decision-making, you will have a unique opportunity to have influence on your own job. You will be implementing regulatory strategy in product development and ensure submissions in EU, US and Canada. You will experience a varied working day in a dynamic organization. You will work closely with your colleagues, particularly colleagues in Denmark, Germany, and Asia.

A job with impact

Your main responsibilities will be:

  • Regulatory activities related to lifecycle management activities for products on the market
  • Vigilance evaluation and reporting

Being part of cross functional teams, you will be working closely together with stakeholders from among others R&D, QA-Engineering, Marketing and Clinical Department.

Key competences

You hold a master's degree in a relevant field of science for example engineering, biology, or another natural science field.

To succeed in the job, you are collaborative, have a structured approach, are proactive and have an eye for the detail while keeping the oversight.

Experience from working with medical devices and design control will be an advantage.

[xxxxx] is a global company and English is our corporate language, which requires that you speak and write English at a high level. You will use English every day in your job.

[xxxxx] – a visionary and international workplace where your efforts matter

We offer a wide range of professional, social, and financial employee benefits along with exciting job challenges and career opportunities contributing to your job satisfaction.

When to apply

As an equal opportunity employer, all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin. If you are ready to apply for the position, please apply as soon as possible.

Whilst this ad might be up until the 25th of August, we will invite candidates for interviews on a continuous basis so no need to hesitate.

The maternity cover will end by October 2025.

For further inquiries please contact, Head of Regulatory Affairs Visualization & Vigilance, Kristine Rasmussen, at krra@[xxxxx].com.

Your application will be treated confidentially.


Information og data

Denne ledige stilling har jobtypen "Apoteker", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i Ballerup.

Jobbet er oprettet på vores service den 4.9.2024, 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.
  • 08.09.2024
  • Apoteker
  • Ballerup

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