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- Tasks: Lead the development of non-invasive therapies and ensure product quality across all departments.
- Company: Join an innovative medical device manufacturer based in Neuchâtel, focused on cutting-edge healthcare solutions.
- Benefits: Enjoy a dynamic work environment with opportunities for professional growth and impactful contributions.
- Why this job: Be part of a senior leadership team driving innovation in medical technology with a focus on quality and efficiency.
- Qualifications: Requires a Bachelor's degree and 10+ years in the medical device industry with strong leadership skills.
- Other info: Experience with regulatory affairs and ISO standards is essential for this role.
The predicted salary is between 72000 - 108000 £ per year.
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, needing an experienced individual to assist in the further development of their non-invasive therapies. The role encompasses all aspects from R&D, quality, and regulatory affairs while working cross-functionally with all departments.
Responsibilities:
- Assure all product quality according to the relevant valid directives are placed on the market in a timely manner and in a most cost-efficient way.
- Lead product and production equipment transformation, modification, adaptation, and development to constantly improve efficiency and quality.
- Oversee the design and introduction of production tools, CAD design tasks.
- Plan, manage and follow-up business objectives, QMS measures and any other task deriving from Management review report.
- Responsible for product registration/certification/approval, particularly with regard to US (510K, PMA) and Canada (MDL).
- Ensure the conformity of products with legal standards and requirements (e.g., EU, USA, China markets).
- Handle and negotiate contracts with external suppliers and other partners.
Requirements:
- Bachelor’s degree in a relevant field.
- 10+ years experience within the medical device industry.
- Proven experience in quality management, regulatory affairs, research and development, and medical device manufacturing.
- Familiarity with ISO 13485 and other relevant quality standards.
- Strong leadership, communication, and problem-solving skills.
- 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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Technical Director, null employer: TN United Kingdom
Contact Detail:
TN United Kingdom Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Technical Director, null
✨Tip Number 1
Make sure to highlight your extensive experience in the medical device industry during networking events or conversations. Connect with professionals who are already in leadership roles within similar companies to gain insights and potentially get referrals.
✨Tip Number 2
Stay updated on the latest trends and regulations in the medical device sector, especially regarding quality management and regulatory affairs. This knowledge will not only help you in interviews but also demonstrate your commitment to the field.
✨Tip Number 3
Consider joining relevant professional organizations or attending industry conferences. These platforms can provide valuable networking opportunities and may lead to connections that can help you land the Technical Director position.
✨Tip Number 4
Prepare to discuss specific examples of how you've led cross-functional teams in past roles. Being able to articulate your leadership style and problem-solving skills will be crucial in demonstrating your fit for this senior position.
We think you need these skills to ace Technical Director, null
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Technical Director position. Understand the key responsibilities and requirements, especially focusing on R&D, quality management, and regulatory affairs.
Tailor Your Resume: Customize your resume to highlight your 10+ years of experience in the medical device industry. Emphasize your proven track record in quality management, regulatory affairs, and leadership skills that align with the job requirements.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for non-invasive therapies and your ability to lead cross-functional teams. Mention specific examples of how you've improved efficiency and quality in previous roles.
Highlight Relevant Certifications: If you have certifications related to ISO 13485 or other relevant quality standards, make sure to include them in your application. This will demonstrate your commitment to quality management in the medical device field.
How to prepare for a job interview at TN United Kingdom
✨Showcase Your Experience
Make sure to highlight your 10+ years of experience in the medical device industry. Be prepared to discuss specific projects where you led R&D, quality management, or regulatory affairs, as this will demonstrate your expertise and suitability for the role.
✨Understand Regulatory Standards
Familiarize yourself with ISO 13485 and other relevant quality standards. During the interview, be ready to explain how you've ensured product conformity with legal standards in previous roles, especially regarding US and Canadian regulations.
✨Demonstrate Leadership Skills
As a Technical Director, strong leadership is crucial. Prepare examples of how you've successfully led cross-functional teams and managed projects. Highlight your communication and problem-solving skills, as these are key to balancing strategic thinking with hands-on execution.
✨Prepare for Technical Questions
Expect technical questions related to product registration, certification, and quality assurance processes. Brush up on your knowledge of non-invasive therapies and be ready to discuss how you would approach product development and efficiency improvements.
