Medical Devices QMS specialist


Job Description:

Braine-l'Alleud - Contracting

  • Managing and keeping up to date the master documentation list and links within the Veeva electronic Content Management System (eCMS)
  • Contributing to writing/reviewing of procedural documents including SOP, work instructions, templates, forms, … while checking consistency across the quality system, ensuring compliance to Documentation Management SOPs, ISO⚠ and ⚠ CFR Part ⚠, and implementing the Global Recruitment Best practices
  • Creating or updating process flows using iGrafx software and reviewing documents' meta data
  • Managing KPIs with monthly extracts, preparation of data and presentation of reports
  • Monitoring and following up with action owners and document owners from other departments
  • Supporting preparation and management of inspections
  • Supporting eQMS implementation by participating in validation activities
  • Support the quality improvement culture

Candidate Requirements:

  • Proficiency in English (written and spoken) is required - French is a bonus
  • Organized, rigorous on details and on keeping to deadlines, quickly learn to use several documentation tools
  • Able to ask more senior colleagues to progress their work
  • Show some initiative within the scope of work

At Global Recruitment, we provide you with a long-term contract that is competitive in terms of salary and increases with experience (company car, meal cards, etc.).

Is it important to you to know the rest of the hiring process? If this sounds like you and you want to learn more, I encourage you to apply!

Next, a recruitment agent will contact you to assess your resume and determine what inspires you. I swear, we'll be nice! We can't wait to see you, so don't delay any longer!

 

Medical Devices QMS specialist

Van 14 augustus 2024 tot 13 oktober 2024

Arbeider
21 EUR
Brabant Wallon
België