Jobid=122d152d2baf (0.1008)
Responsibilities
Be responsible for Post Market regulatory compliance in Europe
Drive process improvements within the team, the department and the organization
Define team goals in line with Applied Medical’s vision and plan
Guide and lead the team members in implementing set goals by creating an empowering and safe environment for them
Act as subject matter expert in Post Market Regulatory related processes
Ensure continuous compliance with all applicable laws and regulations
Monitor and Analyze Post Market data
Create a team member related planning such as onboarding and succession planning, development planning, etc.
What you bring
Bachelor’s degree (HBO) in engineering, life sciences related studies, or similar
At least 5 years’ experience working within a regulatory affairs related discipline
At least 2 years' experience in a supervisory role
Excellent knowledge of major medical device standards and regulations
Excellent oral and written communication skills in English
What we offer
An international working environment, fueled by respect and a healthy work-life balance tailored to the business and team member’s needs
27 paid vacation days (based on fulltime contract) with option to purchase five additional days
This is mainly an on-site role with hybrid options
Commuting allowance of €0,23/km or full coverage of public transportation costs
A wide variety of internal trainings and development possibilities and a tuition program for external trainings
The opportunity to pro-actively work on your vitality and fitness
State-of-the-art facilities, including green areas, in-house restaurant and gym
Additional benefits, such as:Attractive pension scheme (your contribution at 4%, ours at 12%)€50 net monthly health insurance contributionTwo (paid) days per year dedicated to volunteering activitiesSeveral fun company events and meaningful initiatives organized throughout the year
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