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Senior Supplier Quality Manager

Kraj:  PL
Miasto:  Mierzyn

We are looking for an experienced and forward-thinking Senior Supplier Quality Manager to help shape the future of our global Supplier Quality Management organization. In this role you will drive cross-functional quality initiatives, ensure compliance in a regulated medical device environment, and influence strategic direction across our supplier landscape.

Working with us you will receive:

  • full-time work agreement in an international organization;
  • learning and development opportunities, adapted to your needs and supporting your growth;
  • flexible working hours;
  • benefits package including social benefits (private medical health care, insurance,
    sport card, etc.);
  • Scandinavian culture – we are informal and care about equality, independence, open dialog, and work-life balance.

What tasks are waiting for you?

  • Being end-to-end responsible for supplier quality assurance (from concept, through project, NPI, mass production phase, until end-of-life of the product) within given categories; 
  • Playing key role in new suppliers qualification process;
  • Working with outsourced processes (development / manufacturing);
  • Auditing suppliers (Lead auditor role) – QMS and process;
  • Acting as a Lead SQM in new development projects;
  • Close collaboration with R&D, Operations and Product Quality team, within aspects related to supplier quality;
  • Oversight of supplier performance and implementing improvements when needed;
  • Oversight and facilitation of change requests coming from suppliers;
  • Being part of teams, driving cost reductions projects, related to purchased components;
  • Strengthen supplier maturity and performance through proactive engagement.

Apply today if you:

  • Have a minimum of 3 years of working in supplier quality area 
  • Have an experience in working with outsourcing of development and manufacturing of finished devices alternatively with injection moulding and painting processes;
  • Have strong knowledge of ISO 13485, MDSAP, and medical device regulations;
  • Have auditor training and experience, conducting supplier process and system audits;
  • Have strong analytical, communication, and stakeholder management skills;
  • Are self-driven person who likes independence and taking responsibility;
  • Have experience working with global suppliers and in cross-cultural collaboration (considered an advantage);
  • Have technical insight into chipset, electronics, and/or mechanics engineering.

 

 

Please send your CV in English.

 


If you have any questions, contact the recruiter: Ania (asia@demant.com

 

 

#LI-AS1 #LI-ON#Demant_Poland

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