Quality Coordinator

• An innovative, ambitious group committed to public health
• A project driven by passion and purpose
• A team of experts with diverse personalities

We are offering a full-time, permanent position (36.5 hours per week) at our Rovipharm facility in Val-Revermont (01).

Reporting to the Site Quality Manager, you will ensure product compliance and promote quality within the production teams.

In this role, your main responsibilities will be:

Quality in Production:

• Perform product inspections at workstations in accordance with inspection procedures and documentation.
  • Carry out visual inspections.
  • Perform sampling inspections using statistical sampling tables.
  • Verify production records, including traceability documentation.
  • Conduct metrological inspections using company measuring equipment (calipers, scales, height gauges, gauge blocks, and inspection fixtures).
• Ensure that inspection and recording activities carried out by operators and technicians are properly performed.Ensure that inspection and recording activities carried out by operators and technicians are properly performed.
• Participate in the onboarding and training of new production employees.
• Organize sorting and containment operations.
• Contribute to the review and improvement of production inspection procedures.
• Manage non-conformities on a day-to-day basis: escalation, documentation, follow-up, and closure.

Quality:

• Train operators and promote best practices related to quality, Good Manufacturing Practices (GMP), safety, hygiene, housekeeping, and environmental requirements (compliance with inspection procedures, inspection frequencies, work instructions, production order records, etc.).
• Ensure and enforce high standards of hygiene, cleanliness, and workplace organization at production workstations.
• Review batch records and release manufactured batches.
• Escalate any issues or difficulties encountered to the relevant supervisor.
• Support the production team in problem-solving activities and the implementation of corrective actions resulting from internal non-conformities.

Additional responsibilities:

• Serve as a backup for the on-site quality coordinators
• Carry out various tasks for the quality department as needed
• Provide support for new projects.

• You have at least one year of successful experience working within a quality team in an industrial environment.
• You are proficient in Microsoft Office applications and quality control tools.
• You have a good understanding of Good Manufacturing Practices (GMP).
• Knowledge of ISO 13485 is an advantage.
• You demonstrate strong organizational and training/coaching skills.
• You are a team player with excellent interpersonal skills and are recognized for your rigor and attention to detail.
• You are flexible and willing to provide occasional cover for shift-based teams according to department needs.

Do you meet all these criteria? If so, you’re the ideal candidate!

Don’t meet some of the criteria? Give it a try and apply anyway. We’ll carefully review your application!

We are proud to promote diversity and equal opportunity within our teams. We firmly 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 will therefore consider all applications* while fostering an inclusive work culture where every individual can feel they belong.

All applications will be considered regardless of origin, background, religion, sex, sexual orientation, gender identity, disability, etc.