Regulatory Affairs Manager
Location: NetherlandsSIRE 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 organization, based in Limburg Netherlands.
They are a global leader in the medical technology, services and solutions. As being one of the largest medical companies they believe in making a difference with both their products as I in the careers of their employees.
ROLE DESCRIPTION
Being the Regulatory Affairs Manager (RAM) they are looking for someone to strengthen the team as challenges are expected and you will be responsible for making sure that compliancy will be ensured and you coordinate, perform and maintain this regulatory vigilance for the EMEA department. Together with the regulatory specialist team that you will manage, you will design and maintain and efficient and effective process according to all regulatory requirements and company standards.
RESPONSIBILITIES
As the new RAM your main responsibility is assessing, maintaining and improving compliancy to all standards that regard all company products. You will as well serve as contact person between company regions and groups. Other duties and responsibilities might be:
• Preparation and execution of divisional action plans in EMEA and ensuring clear communication and informed cooperation between groups
• Building improvements and/or changes into the EMEA process as necessary on every group, division or region
• Developing, analysing and maintaining all processes regarding your department. Safeguarding all processes’ efficiency and maintaining control that effectiveness stays high
REQUIREMENTS
• University degree preferably in Life Science sector
• 5+ years of relevant working experience within Medical Device or Pharma industry
• Proven experience in management and leadership
• Excellent communication and negotiation skills
• Fluent in English written and spoken
• At least average in IT skills since various tools will be used in day to day work
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jeroen Evertsen.