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Director Quality for Supply Chain & Product Labeling

This job posting is no longer active.

Location: CRAPONNE, France
Position Type: Unfixed Term
Job Function: Quality

A world leader in the field of in vitro diagnostics for over 55 years, bioMérieux conceives, develops, produces and markets diagnostics solutions (systems, reagents, software and services) intended for clinical and industrial applications, which determine the origin of a disease or a contamination to improve the health of patients and insure consumer safety.

bioMérieux is present in 44 countries and serves more than 160 countries with the support of a large network of distributors. Its corporate headquarters are located in Marcy l’Étoile, near Lyon, in France.

Joining bioMérieux is choosing to be a part of an innovative company with a long term vision, committed to the service of public health and carried out with a humanist corporate culture.

Our Company offers numerous opportunities for professional development. You want to  help save lives across the globe? Join the 12,000 employees of bioMérieux!




We are recruiting a Director Quality for Supply Chain & Product Labeling. You will directly report to the Sr. Vice President Quality for Manufacturing & Supply Chain and will manage an international team of around 15 employees.


What will be your responsibilities at bioMérieux?


Capture, analyze and implement good practices, new regulations and customer expectations from a Quality stand point within the global scope of Supply Chain & Product Labeling.


  • Define and maintain SOP’s for global processes related to Supply Chain & Product Labeling,
  • Develop an efficient, robust and sustainable Quality Management System within the supported functions,
  • Ensure global inspection readiness and continuous improvement,
  • Move from the perception of a Quality Function to a Quality Partner and become the single Quality point of contact for Supply Chain & Product Labeling activities
  • Be accountable for Quality related distribution activities (IDC and RDC),
  • Main regulations to master: 21 CFR Part 820, ISO 13485/MDSAP, ISO 9001, IVDD/IVDR/MD/MDR


Who are you ? 

  • Bachelor/Master’s degree with over 12 years of industry experience or equivalent.
  • You have a strong experience in participation in the management of regulatory audits. Your team management skills, your leadership, your pragmatism, your ease in working in the field, as well as strong communication and negotiation skills will succeed in this position.
  • Fluent English.





Working at bioMérieux means being involved long term with a pioneering, visionary and constantly growing company that allows its employees to live a stimulating and inspiring experience in a fulfilling work environment

Our internal mobility policy offers numerous opportunities for each of our 12 000 employees to blossom throughout their career, while respecting each employee’s individual talents as well as their personal and professional development.

At bioMérieux, over 200 professions - both scientific and non-scientific - offer our employees the opportunity to broaden their fields of expertise and develop cross-functional careers. We provide a rewarding experience in an international company that brings together talents from diverse backgrounds, thus fostering a daily aspiration to go beyond the limits.

Helping improve public health around in the world : our mission gives purpose to every profession practiced within the company.

bioMérieux is an Equal Opportunity, Affirmative Action Employer. M/F/Vet/Disability/Sexual Orientation/Gender Identity/GINA.

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