Development Engineer

Straumann seeks a Development Engineer in Basel to lead the technical development of its dental implant systems, ensuring compliance with global medical device regulations.

This position serves as the technical lead for the Straumann Dental Implant Systems (SDIS) portfolio. The engineer reports to the Team Lead for Product Development Instruments and is responsible for guiding complex, cross-functional projects from concept through to design transfer. The role requires occasional travel, up to 10%, to support various project needs.

Responsibilities

• Act as the primary technical authority for challenging, cross-functional development initiatives, strictly adhering to design control protocols and risk management frameworks.
• Assess technical viability and conduct feasibility studies to validate proposed solutions.
• Convert user requirements and applicable standards into concrete design specifications.
• Manage and coordinate verification and validation (V&V) processes.
• Oversee design transfer activities to ensure smooth transition from development to production.
• Analyze business implications arising from design changes or modifications.
• Serve as the technical lead during root cause investigations for product issues.
• Maintain Design History File (DHF) documentation in full compliance with Good Documentation Practices (GDP).
• Act as a subject matter expert during internal and external audits.
• Mentor and supervise students and trainees within the team.
• Provide technical input to support overall portfolio strategy.
• Represent the company in customer interactions.

Requirements

• Bachelor’s degree in mechanical engineering, microengineering, bioengineering, materials science, or a closely related discipline.
• Three to five years of professional experience in medical device development or other highly regulated industries.
• Proven expertise in product development, manufacturing processes, and testing methodologies.
• Deep understanding of relevant standards and regulations, including MDR, FDA, ISO, and ASTM.
• Strong grasp of the design control process.
• Familiarity with medical device manufacturing techniques, such as plastic or metal injection molding, machining, and post-processing.
• Proficiency in development tools including statistical analysis, FMEA, and mechanical property analysis.
• Working knowledge of SAP and PLM systems.
• Experience conducting and participating in quality system audits and inspections.
• Ability to thrive and collaborate effectively within a matrixed organizational structure.

Nice to have

• A Master of Science (M.Sc.) degree is preferred; advanced degrees may be considered equivalent to relevant work experience.

About the company

Straumann is driven by a mission to improve oral health and transform millions of lives globally. The company fosters a high-performance, player-learner culture that encourages collaboration, curiosity, and ambition. Employees are empowered to take ownership of their career paths, leveraging their skills and passion for continuous learning and professional growth.

• Mission-focused work aimed at improving global oral health.
• A high-performance culture that values collaboration and curiosity.
• Opportunities for personal career development and continuous learning.