We are a companythat develops and manufacturesmedical devicesfor therapeutic applicationsand markets them worldwide.
Reporting directly to the General Manager, we are seeking an engineer to join our team. If you are ready to take on this exciting opportunity and possess strong technical skills, apply now for the position of
Tasks
Lead product and production equipment transformation, modification, adaptation and development to constantly improve efficiency and quality
Cover technical aspects of strategic product portfolio, analysis and extensions
Design and introduction of production tools
Responsible of CAD design tasks
Validation of production processes
Responsible of documentation and training of production processes and test procedures
Handle and negotiate contracts with external suppliers and other partners
Assure highest quality products which are placed on the market in a timely manner and in a most cost efficient way
Determine, negotiate and agree in-house quality procedures, standards and specifications in accordance with ISO 13485, MDSAP, EU MDR 2017/745 and another medical device requirements
Verify and monitor quality relevant documents and processes
Assure conformity of products with legal standards and requirements (EU, USA, China markets)
Follow communication with notified body (technical part)
Improve in supply chain of critical components (product quality, reliability and cost effective changes)
Qualifications
Deep understanding of optical engineering principles
Proficiency in electrical engineering, especially as it pertains to light-based technologies
Experience in product development and manufacturing processes
Excellent Knowledge of regulatory requirements and standards in the medical device industry
5 years of experience in medical product registration and experience on Chinese market and competence in the field of transition from MDD to MDR
Strong leadership and project management skills
Ability to collaborate with cross-functional teams
Fluent in Englisch, French is an advantage
You can expect an extremely interesting working environment with challenging tasks in an international environment in which you can develop your area of responsibility and contribute your ideas. We look forward to receiving your complete application documents in English by e-mail to .
BIOPTRON AG, Human Resources, Ms. Silvia Imdorf, .