Service
Regulatory Affairs is a cornerstone in our portfolio. No matter the current regional focus of your product, we help prepare you to succeed.
- Consulting
- Development
- Pharmaceutical industry
Device Development Manager
Suma Medtec GmbH
Kufstein, Austria
Dedicated professional with experience in medical device engineering and development
Skilled in Design Controls, Development Processes, Risk Management, Technical Documentation, Quality Management, and Clinical Product Support
Effective communicator with strong analytical and problem-solving abilities
Passionate about innovation and committed to continuous learning
My organisation
Suma Medtec GmbH is dedicated to offering personalized development solutions for medical device and pharmaceutical companies. With a lasting commitment to patients at the forefront, we specialize in research & development, regulatory intelligence, and strategic planning from ideation through market approval. Our focus extends to risk management and optimizing user experience/human factors. In addition to serving established companies, we are excited to collaborate with startups, offering tailored support.
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Additional questions
Areas od activity
Organization type
ConsultancyService
Regulatory Affairs is a cornerstone in our portfolio. No matter the current regional focus of your product, we help prepare you to succeed.
Service
We integrate risk management and user considerations into the development cycle to reveal effective mitigations and design improvements.
Service
Suma Medtec offers engineering support across all stages of the product life cycle.
Service
Our project management expertise will keep you on track, acknowledge risk, resolve barriers, and enable a winning project team.
Service
Our quality management approach is solution-oriented. We ensure development initiatives can reach the finish line holding a high standard.
Partnership
Suma Medtec - Your life science partner from ideation through development to market.
Consider partnering with Suma Medtec to enable rapid market access for your medical device.