In this role you are responsible for the management of the RA-owned procedural documents and mandatory training for RA GDD worldwide. Your responsibilities include: - Ensure updated and compliant status of RA-owned procedural documents (tracking and coordination of writing) - Support the RA SOPs authors with training and continuous guidance / operational help - Manage training assignment of SOPs /WIs to relevant roles in RA, and maintain RA training curricula information - Support the RA GDD organization for internal global audits related to SOPs and training - Help to devise and implement relevant remedial and improvement actions for Corrective Action Plans from training audits and follow-up on completion and implementation of relevant tasks to ensure closure
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!
Global Pharma Company.
If you are interested then kindly send your resume to: firstname.lastname@example.org
- 5 years Pharmaceutical working experience with preferably experience in Regulatory Affairs - Basic knowledge of global regulatory requirements - Strong quality and compliance mindset - Superior communication, facilitation, negotiation, and problem resolution skills
Degree in Pharmaceutical Sciences or a related discipline
English : Very good