Quality Assurance and Regulatory Affairs Careers

The Quality system and the jobs pertaining to it help guarantee the relevance and efficiency of our work methods to produce the best products and, consequently, the highest level of customer satisfaction.

Regulatory Affairs helps us bring products to market with the competent authorities of all the countries where Stago is represented. The activities of Regulatory Affairs therefore include keeping a regulatory watch and writing manuals and instructions.

Role:

• You deal with complaints and reagent-vigilance files
• You update the specifications of reagents in the context of change management and help manage risks in the post-production stage.

Qualifications:

• You have an engineering degree or Master’s specialized in Biology, Biochemistry or Pharmacy, with experience in quality assurance and/or regulatory affairs in the industrial sector.

Role:

• You assure the registration of products and produce the technical documentation for reagents in accordance with the applicable regulations and production constraints.
• In this way, you contribute to the marketing of the products and the correct use of reagents by customers.

Qualifications:

• You have an engineering degree or Master’s specialized in Biology, Biochemistry or Pharmacy, with experience in medical biology laboratories and/or regulatory affairs.

Role:

• You keep a regulatory watch and inform the departments concerned of any regulatory changes.
• You check that the standards are applied in your field to guarantee that the products sold comply with the applicable regulations.

Qualifications:

• You have an engineering degree or Master’s specialized in Biology, Biochemistry or Pharmacy, with experience in medical biology laboratories and/or regulatory affairs.