Project Quality Officer (M/F)

SGH MEDICAL PHARMARhôneEURESpublished 08/31/2026
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.