Sr. Consultant Regulatory Affairs / Medical Devices

The Netherlands/Europe

Minimum 7 - 10 years working experience in Medical Devices

Is this your DNA? 

Do you find pride in supporting customers in line with professional and ethical values? Do you have a practical approach and like being creative in finding solutions? Please take a look at our career opportunities at Qserve. We would like to get in contact with you!

This is what you will be doing at Qserve:

As a Senior Regulatory Affairs Consultants at our company, you provide specialist consulting services, auditing and/or training in medical device regulations, quality assurance, compliance, clinical evaluation, and strategic support to medical device manufacturers. With the objective to obtain or maintain or expand market access for our customers to various markets (EU, USA, China) and based on predetermined and agreed deliverables. As a consultant, you may build (technical) documentation and design dossiers in support of CE marking, 510(k), or similar approval processes. Your activities may include strategy planning, reviewing and/or developing technical files, clinical evaluations and quality management systems. You may conduct internal or supplier audits, or deliver interim QA/RA management, or help improve our customers quality processes.

 

You maintain, develop and share your expertise and knowledge on a specific expert area. On this specific expert area, you will be the point of contact for colleagues and customers. You will pro-actively follow the news and trends in the market to share in our Knowledge Center. In your expertise area, you will be responsible for writing blogs, whitepapers, news items, presentations or similar to promote our knowledge base and the Qserve brand. 

And this is what you will bring:

  • You have a technical or scientific degree (BSc, MSc or Ph.D.) in physics, mechanical engineering, chemistry, (medical) biology, biomedical technology or similar. 
  • Minimum 7 to 10 years working experience in the field of medical devices through positions in industry, consultancy or regulatory agencies (Notified Bodies, FDA), in either manufacturing, R&D, quality or regulatory roles (e.g. Manager Regulatory Affairs & Quality Assurance). 
  • Knowledge of Medical Device Regulations (CE, FDA, PAL, TGA, etc.) and/or quality assurance.
  • Pragmatic, enjoying a mix of activities in technology, business processes, regulatory affairs, quality assurance or clinical affairs.
  • Communicative and service oriented, supporting a wide variety of clients from small start-ups to large multi-nationals, able to adapt to different company cultures and situations.
  • Strong organizational skills, detailed oriented to deal with various projects at the same time.
  • Fluent in English.
  • Working permit and driver’s license for The Netherlands. 

Why choose Qserve?

Qserve has an international and dynamic work environment in which you can learn, develop and operate in the innovative, fast-moving medical device sector. We offer flexibility and diversity in terms of clients, devices, technology, roles (author, reviewer, expert, trainer, auditor, etc.) and projects. Work together, learn from and be part of a strong international team with technical, regulatory, quality and clinical competences (all together over 500 years of experience). And last but not least we offer a balanced set of core benefits that we believe are important to all employees. 

“Global reach, practical approach, experienced team”

Interested? 

Getting excited about a career as a consultant in the dynamic and innovating world of medical devices? Then please submit your resume and letter of motivation to careers@qservegroup.com or use our application form. For more information about our company, you can always visit our website or contact our HR department at +31 20 78 82 630. 

Location: mainly home-based, but we expect our consultants to work at the client location, from home or from our offices Arnhem or Amsterdam, depending on the need.