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Senior Supplier Quality Engineer (m/f) - Medtech Lausanne, Vaud | LHH

Trouver un emploi | Ressources pour l’emploi et la recherche de carrière LHH

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

RefJN-062024-603166

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

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