At Eurotrol, our Medical Device Development Specialists play a vital role in driving innovation and ensuring excellence in our medical device (in vitro diagnostic) offerings. As a Medical Device Development Specialist, you will be responsible for managing documentation for new products and updates to existing ones, from planning through implementation. Your expertise will help shape the future of our R&D efforts and contribute to our global success.
We’re looking for a proactive and detail-oriented professional with a strong background in (in vitro diagnostic) medical device documentation, project planning, and validation processes. If you thrive in a collaborative environment and are passionate about delivering high-quality results on time, we’d love to hear from you.
Key Responsibilities
- Plan and manage medical device development projects and product changes
- Lead product verification and validation studies
- Perform software validation activities
- Coordinate design transfer with Process Development Engineers
- Lead cross-functional taskforces for product development
- Ensure timely progression through all development phases
- Communicate effectively with customers and internal stakeholders
Qualifications & Skills
- Proven experience in a similar role (preferably within the medical device - in vitro diagnostic-industry)
- Bachelor’s degree or higher (preferably in the field of life sciences)
- Strong project management and deadline-driven mindset
- Exceptional attention to detail and analytical thinking
- Effective problem-solving and decision-making skills
- Excellent verbal and written communication in English
- Team-oriented with a collaborative and positive attitude
- Quality-conscious and committed to continuous improvement
- Ability to foster a productive and communicative work environment
What We Offer
- Competitive employment terms and benefits
- Diverse and autonomous responsibilities
- A professional, supportive and engaging work culture
- Opportunities for personal and professional growth