Project Quality Officer (M/F)
Machine translation — original language: French.Show original
You wish to join:
- An innovative, ambitious group, committed to public health
- A project full of passion and meaning
- An expert team rich in personalities
We offer you:
- A CDD/temporary position for a duration of 9 months
- A position based at our Rovipharm site in Val-Revermont (01) with 3 days of travel per week to be expected on-site and 2 days of remote work possible after the integration period.
- Meal vouchers
- Training in our professions and our products
As part of a maternity leave replacement, we are looking for a Project Quality Officer - Medical devices. Your mission: Reporting to the Site Quality Manager, you are the guarantor of project quality by ensuring proper quality and regulatory documentation in each new product file.
- Manage the risk analysis process
- Facilitate and drive functional analyses / AMDEC at each phase of the project
- Review and/or approve design inputs
- Participate in the drafting of files and the design review
- Collect material certificates of conformity
- Draft Quality documents related to new products
- Verify the presence of documents required by procedures and standards in each file
- Participate in meetings (internal and external) related to product projects
- Propose improvements for product quality
- Ensure project follow-up from a quality and regulatory perspective
- Draft product presentation sheets
- Participate in drafting control ranges and packaging sheets
- Ensure quality follow-up for new projects
- Participate in the testing of new installations
- Follow the Commissioning and Qualification phases of equipment - QC, FAT, SAT, QI, QO, QP
- Participate in field quality audits
- Participate in supplier audits (as part of new projects)
- Participate in the update or creation of QMS documents
- Guide technical teams toward problem-solving and the launch of corrective actions following non-conformities.
Profile sought:
- Higher education in quality / biomedical or plastics engineering, you have at least 1 year of professional experience in project quality, acquired through employment, an internship, or an apprenticeship.
- Knowledge of the ISO 13485 standard
- Good level of professional English
Your assets
- Leadership and the ability to unite multidisciplinary teams.
- Organizational skills and priority management.
- Excellent analytical and problem-solving skills.
- Interpersonal skills and communication aptitude.
- Rigor, autonomy, and initiative.
A great opportunity for a recent graduate! Do you not tick all the boxes? Apply anyway! Your motivation and your ability to quickly develop skills will count just as much.