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Join MRC Holland

MRC Holland has been paving the way to copy number confidence for over a decade. As the inventors and manufacturers of MLPA, we supply the world with simple solutions to genetic inquiries.

As a successful, growing biotechnology company located in Amsterdam, the Netherlands, we offer a young, dynamic, and multi-national working environment. If you are passionate about providing the world with simple and affordable solutions to detect genetic aberrations, and enjoy a vibrant, family-friendly work environment: come join our team!

Read what our employees have to say about MRC Holland.
 

Regulatory Affairs (RA) Specialist (32 hr/wk)

As MRC Holland’s Regulatory Affairs Specialist, you assist in ensuring that MRC Holland and its products meet regulatory requirements for its target markets in a swift manner that is compatible with other MRC objectives. This function requires understanding of the regulatory requirements applicable to In Vitro Diagnostics and Research Use Only products in the target markets. The Regulatory Affairs Specialist assists in the submission of registration files to relevant competent authorities and / or Notified Bodies, and collaborates with QA, Product Development and Technical Support departments to achieve departmental goals. You report directly to the RA Manager.

Responsibilities

  • Assist in the coordination of preparation of registration files for specific target markets for new products, product changes and re-registrations as needed, in compliance with internal procedures and relevant regulatory requirements for the particular jurisdiction.
  • Responsible for the quality of RA-related design project deliverables and documentation.
  • Stay informed on new developments in relevant (inter-)national legislations and regulations on IVDs and assist in implementation activities.
  • Contribute to quality assurance within the department.
  • Keep the RA Manager informed on the progress of project activities.

Qualifications

  • MSc degree in Biology or Biomedical Sciences or equivalent.

Requirements

  • Adequate knowledge of relevant international regulations regarding IVDs (e.g. ISO 13485, European IVD Directive (98/79/EC), European IVD Regulation (EU 2017/746)). 
  • Adequate knowledge of genetics.
  • Advanced technical writing skills in English.
  • Well-developed analytical skills.
  • Affinity with procedures and systems.
  • Self-motivated.
  • Strong organizational skills, flexible, ability to manage multiple tasks and meticulous attention to detail.
  • Able to work independently as well as part of a team.

What do we have to offer?

MRC Holland is a medium sized, flexible organization with colleagues from different cultural backgrounds, where working independently and professionalism are important values.

In addition, we have excellent working conditions. At MRC Holland, besides 28 vacation days a year, we are closed between Christmas and New Year's Day. We have an excellent pension plan, a comprehensive travel allowance, and collective health insurance with a partial reimbursement from MRC Holland. Finally, we offer a reimbursement of (max.) €25 a month for your sports subscription, and you can participate in weekly in-house yoga class or Dutch lessons.

Interested?

Please send your motivation letter and curriculum vitae to apply@mrcholland.com. For more information, contact Johanneke Oud (through apply@mrcholland.com). 

Only applicants who are currently residing in the Netherlands and possess a valid working permit will be considered. For more information on our company and products, visit www.mrcholland.com.

 

Acquisitie naar aanleiding van deze advertentie wordt niet op prijs gesteld.

Only direct applications are welcome.

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