Oversee the regulatory Quality area related to Facilities, including the investigation of non-conforming events, CAPA, commissioning, validations and re-certifications of ISO8 controlled rooms and compressed air systems, as well as internal and external audits, and the review and oversight of documentation (SOPs).

Necessary requirements:

Education: Bachelor's degree in mechanical, industrial, electrical or industrial maintenance engineering

Experience: At least 4 years of experience related to medical industry regulations

English Level: B2