Job Opportunity: Technical Director
An innovative medical device manufacturer based in Neuchâtel is expanding their senior leadership team. They are looking for a Technical Director to join their expanding team, seeking an experienced individual to assist in the further development of their non-invasive therapies. The role encompasses all aspects from R&D, quality, regulatory affairs whilst working cross-functionally with all departments.
Responsibilities:
1. Assure all product quality according to the relevant valid directives are placed on the market in a timely manner and in the most cost-efficient way.
2. Lead product and production equipment transformation, modification, adaptation, and development to constantly improve efficiency and quality.
3. Oversee the design and introduction of production tools, CAD design tasks.
4. Plan, manage and follow-up business objectives, QMS measures and any other tasks deriving from the Management review report.
5. Responsible for product registration / certification / approval, particularly with regard to US (510K, PMA) and Canada (MDL).
6. Ensure the conformity of products with legal standards and requirements (e.g. EU, USA, China markets).
7. Handle and negotiate contracts with external suppliers and other partners.
Requirements:
1. Bachelor's degree in a relevant field.
2. 10+ years experience within the medical device industry.
3. Proven experience in quality management, regulatory affairs, research and development, and medical device manufacturing.
4. Familiarity with ISO 13485 and other relevant quality standards.
5. Strong leadership, communication, and problem-solving skills.
6. Ability to balance strategic thinking with hands-on execution.
If interested, please reach out with an updated version of your resume.
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