About MedTech

Key Responsibilities:

Design & Development:

• Lead and execute detailed engineering design, testing, and validation activities for existing and new products.

• Develop and refine product features and specifications in collaboration with cross-functional teams.

• Support design for manufacturability, cost efficiency, and compliance with all industry standards and regulations.

Product Lifecycle & Sustaining Engineering:

• Support ongoing product lifecycle initiatives including product updates, improvements, and troubleshooting.

• Drive root cause analysis and troubleshooting for field issues, escalation of sustaining engineering requests, and product escalations.

• Implement enhancements aimed at operational efficiency, performance, and quality improvements across the product lifecycle.

Cross-Functional Collaboration:

• Work closely with internal teams such as R&D, manufacturing, supply chain, quality, and external partners to drive project success.

• Provide technical guidance during sourcing, external development, and external manufacturing processes.

• Assist in defining product features, technical requirements, and specifications aligned with business needs.

Regulatory & Quality Support:

• Ensure engineering activities align with regulatory requirements and internal quality standards.

• Support documentation, validation, and verification activities to maintain compliance

Process Optimization & Continuous Improvement:

• Identify opportunities for process improvements, automation, and design optimizations to enhance product quality and operational scalability.

• Leverage best practices in engineering and design for continuous improvement initiatives

Technical Leadership & Expertise

• Serve as a technical resource and mentor to junior engineers and other team members.

• Stay informed on industry trends, emerging technologies, and regulatory updates relevant to cardiovascular product platforms and MedTech

Qualifications:

• Bachelor’s degree in Engineering (Mechanical, Biomedical, or related); Master’s preferred

• 8+ years of experience in medical device engineering, product development, or sustaining engineering

• Deep technical expertise in cardiovascular or related medical device platforms is strongly preferred

• Experience supporting regulated product development (FDA, ISO, IEC standards)

• Strong problem-solving, communication, and team collaboration skills

• Ability to manage multiple projects efficiently and proactively

• Hands on experience with suppliers and manufacturing process development such as injection molding, machining or extrusion strongly preferred.

• Good German and excellent English language skills

The anticipated base pay range for this position is 75.000 to 118.450 EUR.

Required Skills:

Preferred Skills: