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What you can expect

• Your path is taking you into a growing team – and right into our diversity of projects.
• Your task: Preparation of documents for conformity assessments (risk assessments, biological evaluations, clinical evaluations, etc.) of all types of medical devices
• Your mission: In collaboration with your colleagues, you will perform literature and database searches, identify and appraise pertinent data and advise our customers. You will prepare parts of the technical documentation according to current regulations, standards and guidance documents, while being engaged in various regulatory projects.
• Your focus: to obtain approvals/certifications for our client’s medical devices

What You offer

• Science degree in medicine/biology/chemistry/toxicology or related scientific disciplines
• Knowledge in the sphere of toxicological tests, clinical research methodology, information management and regulatory requirements
• Preferably at least 5 years’ experience in medical device regulatory affairs
• Confident use of relevant databases and current office programs
• Ability to tackle and coordinate complex issues effectively
  
• A talent for organisation, goal orientation and awareness of deadlines
• Strong communication and presentation skills
  

What We Offer

• Flexible working hours as well as the possibility of mobile working
• Job Bike
• Intensive on-the-job training and opportunities for personal and professional development
• An appreciative working environment
• An attractive salary with profit-sharing, bonuses and benefits (company pension plan, food allowance, etc.)
  
• A very good working atmosphere in a team supported by corporate events and socialising outside of work