Regulatory Affairs Consultant






MindCapture is a talent and consultancy company, providing advanced consultancy solutions to the biotech, pharma, medical devices, IVD, lab, healthcare and the chemical industry.


At MindCapture we are always looking to expand our team with RA experts. Haven’t found your dream RA job yet? Apply for an open application and we will get in touch with you.

As a RA specialist you are responsible for following the legislation within the pharmaceutical and/or medical devices industry.

  • Provide support to regional and international regulatory strategies and project/product submission plans.

  • Write and adapt regional and international documentation for submissions.

  • Anticipate issues that arise during the product lifecycle.

  • Monitor and respond as necessary to regulatory changes in assigned regions (EMA, FDA).

  • Lead or provide input to internal corporate regulatory initiatives and cross-functional workgroups.


  • Master’s degree in life sciences.

  • You have at least 1 year of relevant RA experience.

  • The pharmaceutical or medical devices regulations (GMP OR ISO13485) have no secrets for you.

  • You speak fluently Dutch and English.


MindCapture offers a dynamic and rewarding work environment. We have a strong focus on candidates and believe in long-term relationships that thrive on quality contacts and insights into career opportunities. Not only for our candidates, but also for our consultants, recruiters and support staff.

We offer strong compensation packages that reward your abilities, hard work and ingenuity in achieving success. We reward you with competitive wages and offer a strong package with additional legal benefits such as meal vouchers, eco vouchers, high health insurance (DKV) and group insurance. Depending on your seniority, a car may be provided.

We provide personalised training to let you grow in the area of

  • What you like to do

  • What you are good at

  • Where and how you want to have an impact

Job application