Responsibilities:

• Write various protocols and documents used for validation in accordance with the standards established by the company and GMP regulations and revise those prepared by third parties;
• Execute qualification / validation protocols according to established procedures;
• Support the resolution of deficiencies resulting from validation;
• Perform additional tests related to closing impairments and CAPA;
• Work in collaboration with project engineering, process development, regulatory and quality assurance staff so that sterile activity requirements are adequately taken into account.

Qualifications and aptitudes:

• Hold a bachelor’s degree in engineering or science, combined with 1 to 3 years of similar experience;
• Be bilingual (FR and EN), both written and spoken;
• Have a good knowledge of good manufacturing practices (GMP);
• Demonstrate rigor in carrying out their mandates and show flexibility to quickly adapt to operational needs;
• Be able to work independently and in a team.

Why join Sterinova?

We are a dynamic team that is constantly looking to go further. We rely on each member of our team, on their background and aptitude to help us achieve our goals and achieve our ambitions.

Sterinova offers you a healthy, team-oriented work environment where people come first. Your work will make a real difference in the hospital market, creating a niche product that saves and prolongs lives.

Joining Sterinova means joining a team where opportunities and possibilities are growing.