Loading

13 Qualitätsmanagement jobs in Morges found

Subscribe to new Qualitätsmanagement jobs in Morges

Loading

Subscribe to new Qualitätsmanagement jobs in Morges

Loading

Other vacancies in the Morges region

You can also find other vacancies in the region Morges in the following locations

;
Loading

Quality Management System Expert

add review
Rating submitted
24/04/2024 100% Permanent position
Work at Michael Page Switzerland
Michael Page Switzerland
  • International company
  • Medical devices
Quality Management System Expert

Our client is an international company specialized in medical devices.

Description

  • Lead identification, development, architecture, and optimizations of the Quality Management System, at both Global and Site levels.
  • Work collaboratively and support process owners in reviewing, structuring, and documenting their functional new or improved processes.
  • Analyze existing processes and ensure integration and consistency across shared, linked, and cross-functionally dependent processes.
  • Author procedures, policies, work instructions, and related documents with style, content, and format guidelines in compliance with ISO 13485, 21CFR820, EU MDR and other applicable regulations.
  • Actively monitor effectiveness of the quality management system and propose and execute improvement projects.
  • Lead complex quality initiatives (e.g. CAPA, process improvements, new processes, gap analyses, system integrations), make recommendations, develop and execute plans.
  • Plan and conduct internal audits by participating and leading internal audits, follow up on the findings with auditee through effective closure, and present the data for trending.
  • Support electronic QMS transition and take ownership of the software tools including QMS documentation and change control.

Profile

  • Degree in Engineering, Scientific.
  • 7+ years of quality-related system experience in a medical device company developing medical devices.
  • Excellent technical writing, proofing, and language (grammar and spelling) skills with strict attention to detail.
  • Significant knowledge of medical device Quality Management Systems (ISO 13485, 21 CFR 820) and regulatory landscape (i.e. MDR).
  • Excellent communication skills and interpersonal relationship skills including negotiating and relationship management skills.
  • Advanced problem-solving, organizational, analytical and critical thinking skills.
  • Certified lead auditor.
  • Electronic QMS experience is preferred.
  • Excellent command of English language.

Job Offer

Great opportunity to join an amazing team and work on challenging projects.

Contact


About the company

1,9 (9 reviews)

Loading

Be notified of new vacancies