Azienda

DanaherVedi altro

addressIndirizzoLocation Bronshoj, Denmark
CategoriaMarketing

Descrizione del lavoro

In our line of work, life isn’t a given - it’s the ultimate goal. When life takes an unexpected turn, our technology and solutions enable caregivers to make informed diagnostic decisions to improve patient care. This is our shared purpose at Radiometer and what unites all +4000 of us - no matter our roles or where in the world we’re located. Creating impactful innovations like ours, doesn’t happen overnight - it requires uncompromising persistency, passion, and a desire to make a difference. Here, you can learn, grow, and chart an uncommonly diverse career. 

Radiometer is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges. 

The Regulatory Affairs Manager at Radiometer is responsible for managing the preparation and submission of the required documentation for product registration, approval, and compliance with international regulations. This role is critical for ensuring that Radiometer's products can be sold in markets around the world. In addition, the Regulatory Affairs Manager is tasked with improving the efficiency and effectiveness of the Regulatory Affairs department's processes, which will help Radiometer navigate complex regulatory environments more easily.

This position is part of the Global Regulatory Affairs department located in Brønshøj, Denmark and will be Hybrid position. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses.

You will be a part of the International Registration team and report to the Global Director for RA, who are responsible for overseeing and ensuring the market access is maintained worldwide. If you thrive in a fast-paced environment, is used to playing a critical supporting role and want to work to build a world-class efficient team that is part of a Global RA department and have interactions and stakeholders to connect with in a global scale - read on.

In this role, you will have the opportunity to:

  • Ensure regulatory compliance to maintain market approvals
  • Lead a team of skilled RA associates
  • Ensure alignment with relevant stakeholders
  • Secure continued support to the RA Regulatory Intelligence process, including stakeholder management with local RA
  • Manage and resource RA support to commercial release
  • Plan and execute projects for new regulatory requirements

The essential requirements of the job include:

  • Master degree, e.g. engineering, biotechnology, pharmaceutical sciences, medical technology or similar science field
  • At least 3 years’ experience in Regulatory Affairs within In vitro Diagnostic Devices or Medical Devices
  • Experience as a people manager
  • Experience with cross-functional work
  • Core Team member for complex development or maintenance project, e.g., spanning across a portfolio, rather than a single product
  • Experience with cross-cultural collaboration

Radiometer

At Radiometer we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Radiometer can provide.

Application

We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application.

We thank you for your interest. Please read our Applicant Data Privacy Notice carefully here.

Hybrid

At Radiometer we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Radiometer can provide. 

Danaher

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Refer code: 1710331. Danaher - Il giorno precedente - 2024-06-12 03:55

Danaher

Location Bronshoj, Denmark

Condividi lavori con gli amici

Lavori correlati

Regulatory Affairs Manager

Quality Assurance Regulatory Affairs Manager

Gruppo Veronesi

Verona, Veneto

una settimana fa - visto

REGULATORY AFFAIRS MANAGER

Biopharmed

Pisa, Toscana

2 settimane fa - visto

Regulatory Affairs Manager

Danaher

Location O'Callaghan Mills, Ireland

un mese fa - visto

Senior Manager, Regulatory Affairs  

Guarda Altre Offerte

it

un mese fa - visto

Regulatory Affairs Senior Manager  

Antal International

Modena, Emilia-Romagna

2 mesi fa - visto

Regulatory Affairs Manager

Unilever

Col. Bosques de las Lomas, Mexico City

2 mesi fa - visto

Senior Regulatory Affairs amp Market Manager

Oatly Ab

Reggio Nell'Emilia, Emilia-Romagna

3 mesi fa - visto

REGULATORY AFFAIRS MANAGER Settore COSMETICO - Milano  

Adecco Italia

Milan, Lombardy, it

4 mesi fa - visto

Manager, Regulatory Affairs

Thermo Fisher Scientific

Frosinone, Lazio

4 mesi fa - visto

Regulatory Affairs Manager Settore Cosmetico - Milano

Adecco Italia

Milano, Lombardia

4 mesi fa - visto

Regulatory Affairs Manager Settore Medical Device - Milano

Adecco Italia

Milano, Lombardia

4 mesi fa - visto

Senior Regulatory Affairs Manager

Abbott

Location Japan - Matsudo-shi

5 mesi fa - visto

REGULATORY AFFAIRS MANAGER

Philogen

Siena, Toscana

5 mesi fa - visto

Regulatory Affairs Manager

F. Hoffmann-La Roche Gruppe

Monza, Lombardia

5 mesi fa - visto

Regulatory Affairs Manager

iAgora

Medicina, Emilia-Romagna

5 mesi fa - visto

Manager, CMC Regulatory Affairs, Global Rare Diseases

iAgora

Scienza/Ricerca, Inglese

6 mesi fa - visto

Manager, CMC Regulatory Affairs, Global Rare Diseases

Chiesi Farmaceutici

Parma, Emilia-Romagna

6 mesi fa - visto