Technical R&D Manager
job details
For one of our Medical device client, we are looking for aTechnical R&D Manager
to support their production.If you are an engineer with already experience in medical devices, this job is for you.
Location: Neuchâtel Canton
Contract: Permanent
Your tasks:
As aTechnical R&D Manager, your primary responsibilities will include:
- Leading product and production equipment transformation for improved efficiency and quality.
- Handling technical aspects of strategic product portfolio, analysis, and extensions.
- Designing and introducing production tools, along with CAD design tasks.
- Establish, negotiate, and reach consensus on internal quality protocols, norms, and criteria aligned with ISO 13485, MDSAP, EU MDR 2017/745, and other relevant medical device standards
- Validating production processes and ensuring all products conform to legal standards and requirements.
- Handling contracts with external suppliers and partners.
Your Profile:
- Deep understanding of optical engineering principles.
- Proficiency in electrical engineering
- Experience in product development and manufacturing processes.
- Excellent knowledge of regulatory requirements and standards in the medical device industry.
- Minimum of 5 years of experience in medical product registration 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 English, French is a plus
For one of our Medical device client, we are looking for aTechnical R&D Manager
to support their production.If you are an engineer with already experience in medical devices, this job is for you.
Location: Neuchâtel Canton
Contract: Permanent
Your tasks:
As aTechnical R&D Manager, your primary responsibilities will include:
- Leading product and production equipment transformation for improved efficiency and quality.
- Handling technical aspects of strategic product portfolio, analysis, and extensions.
- Designing and introducing production tools, along with CAD design tasks.
- Establish, negotiate, and reach consensus on internal quality protocols, norms, and criteria aligned with ISO 13485, MDSAP, EU MDR 2017/745, and other relevant medical device standards
- Validating production processes and ensuring all products conform to legal standards and requirements.
- Handling contracts with external suppliers and partners.
Your Profile:
- Deep understanding of optical engineering principles.
- Proficiency in electrical engineering
- Experience in product development and manufacturing processes.
- Excellent knowledge of regulatory requirements and standards in the medical device industry.
- Minimum of 5 years of experience in medical product registration 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 English, French is a plus
À propos de l'entreprise
