Senior Supplier Quality Engineer (m/f) - Medtech
Lausanne, Vaud
CDI
Santé & thérapie
LHH Recruitment Solutions is a specialized talent recruitment boutique. We provide tailored services to help companies find the best candidates for their staffing needs.
With deep industry expertise and a commitment to excellence, LHH RS is a trusted partner in Switzerland for many years.
Our client is a fast growing MedTech in Lausanne.
Responsibilities :
- Lead suppliers’ qualification audits and related audits follow up according to plan ;
- Ensure suppliers’ management activities according to standard procedure ;
- Manage NC & CAPA (audits, incoming, production issues) ;
- Contribute on ERP and QMS changes (new/update inspection plans, QA items configuration, procedures) ;
- Define and participate on continuous improvements of products and processes (lean six sigma, etc.) ;
- Participate on monitoring CMOs KPIs, data trend analysis and Product Quality Reviews.
Profile :
- Master’s degree in Engineering or Manufacturing (mechanical, electronics) or operational quality,
- At least 5 years’ experience in Manufacturing engineering within the Medical Device industry or similar ;
- External Lead Auditor certificate to perform audits according to ISO 13485 and 9001 ;
- English Fluent, French & German a plus.
Permanent Contract
Senior Supplier Quality Engineer (m/f) - Medtech
LHH
10 il y a quelques jours
CDI
Santé & thérapie
Lausanne, Vaud
LHH Recruitment Solutions is a specialized talent recruitment boutique. We provide tailored services to help companies find the best candidates for their staffing needs.
With deep industry expertise and a commitment to excellence, LHH RS is a trusted partner in Switzerland for many years.
Our client is a fast growing MedTech in Lausanne.
Responsibilities :
- Lead suppliers’ qualification audits and related audits follow up according to plan ;
- Ensure suppliers’ management activities according to standard procedure ;
- Manage NC & CAPA (audits, incoming, production issues) ;
- Contribute on ERP and QMS changes (new/update inspection plans, QA items configuration, procedures) ;
- Define and participate on continuous improvements of products and processes (lean six sigma, etc.) ;
- Participate on monitoring CMOs KPIs, data trend analysis and Product Quality Reviews.
Profile :
- Master’s degree in Engineering or Manufacturing (mechanical, electronics) or operational quality,
- At least 5 years’ experience in Manufacturing engineering within the Medical Device industry or similar ;
- External Lead Auditor certificate to perform audits according to ISO 13485 and 9001 ;
- English Fluent, French & German a plus.
Permanent Contract