Medical Devices Qms Specialist - Braine-l'Alleud, België - Jefferson Wells
Beschrijving
Location:
Braine-l'Alleud
#24003
Medical Devices QMS specialist:
Braine-l'Alleud - Contracting
What do we expect from you?:
- 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, ISO13485 and 21 CFR Part 4, and implementing the SOP Simplification 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
- 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.
What can we offer you?:
At Jefferson Wells, we offer you an indefinite contract, with a competitive salary commensurate with your experience (company car, meal vouchers, etc.).
Do you want to know the rest of the recruitment process?
If this sounds like you and you're keen to find out more, I urge you to apply
Then, in the next few days, a recruiter will get in touch with you to go through your CV and find out what motivates you.
We can't wait to meet you, so don't wait any longer
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