Medical Device Quality Lead (7-Month Contract) Remote

SGH Medical Pharma company; Enclos Rousset; Hybrid; EUR 33,000 - 47,000; Full time

Benefits offered by this job

Remote work after induction (2 days)

Training in business areas and product

Job summary

SGH Medical Pharma Group invites applications for a Project Quality Officer (M/F) for Medical Devices, based at the Rovipharm site in Val-Revermont (01). The role drives quality and regulatory documentation for new product dossiers and supports audits, risk analyses, and design reviews.

The successful candidate will have 3+ years in a similar role, ISO 13485 proficiency, and English language skills, with two remote work days after induction as part of a hybrid arrangement.

Qualifications

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

Responsibilities

• Manage the risk analysis process.
• Lead and oversee FMEA at each stage of the project.
• Draft quality documents relating to new products.
• Attend meetings relating to product projects.
• Monitor projects from a quality and regulatory perspective.
• Assist in drafting inspection procedures and packaging specifications.
• Monitor the quality of new projects.
• Guide technical teams in problem-solving and corrective actions following non-conformities.

Skills

Quality assurance

Regulatory knowledge

Leadership

English proficiency

Education

Higher education in QA/biomedical engineering/plastics

Job description

SGH Medical Pharma Group invites applications for a Project Quality Officer (M/F) for Medical Devices, based at the Rovipharm site in Val-Revermont (01). The role drives quality and regulatory documentation for new product dossiers and supports audits, risk analyses, and design reviews.

The successful candidate will have 3+ years in a similar role, ISO 13485 proficiency, and English language skills, with two remote work days after induction as part of a hybrid arrangement.