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 represented. The activities of Regulatory Affairs therefore include keeping a regulatory watch and writing manuals and instructions.
Testimony
Some examples of jobs in Quality Assurance and Regulatory Affairs:
Product Risk Management Engineer/Manager
Role:
- In collaboration with the different quality managers from R&D and production, you guarantee the identification and management of patient, operator and environmental risks inherent to the instruments and reagents sold by the company.
Qualifications:
- You have an engineering degree or Master’s specialized in Biology, Biochemistry or Pharmacy, with experience in quality assurance and/or risk management in the industrial sector.
Regulatory Records Engineer/Manager
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.
Regulatory Affairs Engineer/Manager
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.