Distalmotion believes that every patient undergoing minimal invasive surgery should benefit from the best of surgical expertise and robotic technology. This is the vision that made us create Dexter, the world’s first and only on-demand robotic surgery system. Thanks to Dexter, surgeons have never been closer to their patients while benefiting from robotic best-in-class technology.

Distalmotion has been created in 2012 by passionate and open-minded people with various experiences. Today, we are still convinced that an inclusive and international company culture is the best way to continue growing. Our leadership is highly committed to promote diversity among the teams and welcome every employee based on their identity.

About Product & Supplier Quality Engineer

Support Product & Supplier Quality department on supplier quality activities namely suppliers’ qualification process and product quality activities for Distalmotion manufacturing lines for sterile instruments, Dexter robot system and its accessories.

Tasks:

Supplier Quality:

• Manage and execute suppliers’ qualification audits and related audits follow up according to audit plan,


• Ensure suppliers’ management activities according to standard DM procedure,


• Manage nonconformities from suppliers (audits, incoming, production issues) and CAPA plans defined by suppliers and follow up.

Product quality:

• Contribute on needed changes on ERP / QMS systems (new/update inspection plans, QA items configuration, procedures),


• Define and participate on continuous improvements of our products and processes (lean six sigma, etc.),


• Participate on monitoring CMOs KPIs, data trend analysis and Product Quality Reviews.

Requirements:

• Bachelor’s degree in an engineering science (mechanical, electronics) or operational quality,
  4-6+ years’ experience in Design or Manufacturing engineering within the Medical Device industry or similar,


• External Lead Auditor certificate to perform audits according to ISO 13485 and 9001,


• Experienced / trained on ISO 13485 and 9001 standards,


• Experience in non-conformities and CAPA management,


• Proven experience on KPI measurement, quality reports and data trending / analysis,


• Manufacturing and engineering skills - knowledge of manufacturing and production processes, process enhancement (provide guidance on improving process efficiency while maintaining a high level of quality, safety, and reliability),


• Excellent written and verbal in-house and external communication and liaison skills,


• English Fluent, French & German a plus,


• Open to travel – up to 30% (all world).

Benefits:

• Opportunity to work in a fast-growing company active in one of the most promising fields of medicine.


• Permanent contract with 25 days of paid vacation.


• A dynamic atmosphere in an internationally minded environment.


• Benefit from one day per week working remotely to boost flexibility.


• Other benefits : Mobility plan, competitive company pension plan, support for gym memberships.


• Regular team building events such as boot camps, skiing and much more.

 

Apply Here