This role will take ownership of the daily execution of the EU QMS—including complaint handling, CAPA, RMA/repair records, and document control. Key Responsibilities · Receive, log, triage, and perform initial vigilance assessments for product complaints originating
Are you passionate about biotechnology and business development? Do you enjoy building strategic partnerships, identifying new commercial opportunities and helping innovative technologies gain traction within the biotech and cell therapy market? We are looking for a