Project Quality Manager – Medical Devices

The SGH Medical Pharma Group is a European leader in medical devices and drug delivery. Building on recent major developments in the field of IVD and as a recipient of funding under the “Industrial Modernization” recovery plan, our group continues to grow and strengthen its structure.

offers a comprehensive range of services, from standard production to custom development, including medical contract manufacturing. In addition to manufacturing at multiple ISO 13485 / 15378 / 14001-certified sites—some of which are ISO 8 cleanrooms—we make our full range of expertise in quality, R&D, industrialization, and marketing available to our customers.

You want to join

An innovative, ambitious company committed to public health, with a project that’s both passionate and meaningful, as part of an expert team full of diverse personalities? We are offering an excellent opportunity for a fixed-term or temporary position of 6 months as a Project Quality Manager – Medical Devices at our Val-Revermont (01) site.

We offer

• A fixed-term or temporary position with a start date between August 24, 2026, and September 1, 2026
  • For a period of 6 months
  • As part of a maternity leave replacement
• Training on our business areas and products

Your missions

Reporting to the Site Quality Manager , you are responsible for ensuring the quality of projects by making sure that all quality and regulatory documentation is properly maintained for each new product file.

• Manage the risk analysis process
• Facilitate and oversee functional analyses and FMEA at each project phase
• Participate in the preparation of documentation and design reviews
• Obtain material compliance certificates
• Draft quality documents related to new products
• Verify that all documents required by procedures and standards are included in each file
• Participate in meetings (internal and external) related to product projects
• Propose improvements to product quality
• Monitor projects from a quality and regulatory perspective
• Draft product presentation sheets
• Participate in drafting inspection procedures and packaging sheets
• Ensure quality monitoring of new projects
• Participate in testing new installations
• Monitor the commissioning and qualification phases of equipment—QC, FAT, SAT, QI, QO, QP
• Participate in on-site quality audits
• Participate in supplier audits (as part of new projects)
• Participate in updating or creating QMS documents
• Guide technical teams in troubleshooting and implementing corrective actions following nonconformities.

Desired candidate profile

• Higher education in quality assurance, biomedical engineering, or plastics processing
• At least 3 years of proven experience in a similar role
• Proficiency in the ISO 13485 standard
• Industry experience (plastics processing or medical devices)

Your strengths

• Leadership and the ability to bring together multidisciplinary teams.
• Strong organizational skills and the ability to manage priorities.
• Excellent analytical and problem-solving skills.
• Strong interpersonal and communication skills.
• Attention to detail, independence, and a proactive approach.

Do you have all these skills? If so, you’re the ideal candidate!

Missing a few? Give it a try and apply. We’ll review your application carefully!

We’re proud to promote diversity and equal opportunity within our teams. We believe that our differences make a difference and that an inclusive work environment will foster our growth as a company, as teams, and as individuals. We’ll therefore consider all applications while fostering an inclusive work culture where everyone feels they belong.