RA manager Benelux
Location: BelgiumSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Medical Devices and Pharmaceutical organization, based in Belgium.
This organisation is completely focused on our health. They offer products for both the professional healthcare takers as for us, consumers. They offer a broad scale of services varying from nutrition to diagnostics, and from diabetes care to pharmaceuticals. This organisation collaborates with another key player within pharmaceuticals,which takes there company to a next level.
ROLE DESCRIPTION
In your role as Regulatory affairs manager you are responsible for the control of all regulatory related activities within the Benelux. Next to that you will also take the responsibility to establish relationships with competent authorities and agencies who you will interact with on a frequent basis. In addition, you will be responsible to investigate the market and implement relevant regulations. You are the key in the maintenance of relationships with external stakeholders such as public agencies. This job is set for a year with possible extension to 2.5 years.
RESPONSIBILITIES
As a RA manager you are completely involved in all regulatory affairs and regulations concerning the company’s products. Next to that you will overview all required documentations both for European and international level. Further responsibilities are:
• Interaction with internal and external stakeholders among which national and European governmental associations
• Mentor of your team in which you provide the required knowledge
• Supportive role as advisor on strategies and actions among RA
• Creating application tools and planning for product regulations
• Creating awareness across various departments for the matter of RA
• Interaction with the overall Benelux manager
REQUIREMENTS
• Master’s degree in Life Sciences
• Minimal 2 years of experience within RA in Medical Devices sector
• Minimal 2 years of experience in management role within Healthcare/ Medical Device organisation
• Evidence of previous interaction with governmental bodies and authorities
• Fluency in Dutch, French and English
• Excellent communication and (technical) written skills
• A team player
• Dares to be challenged
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Juliette van Kraaij.
