-
(such as, Development Operations, Pharmaceutical Sciences, Safety Risk Management, Regulatory), and external regulatory, industry, professional and academic organizations. Ensure that all study and project
-
changing needs of the regulatory environment Works with RQA colleagues on cross GxP audit plans as required Coaches colleagues - leads training for routine and non-routine site and process audits Advises
Enter an email to receive alerts for industrial-phd "CERN European Organization for Nuclear Research" positions