We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as M M&S Services, PV & Medical - Quality training coordinator within M&S Quality, you will be :

Main responsibilities:

• Contribute to the development of the global strategy of training for all Pharmacovigilance and Medical associates (PSPV, Medical GBUs, Countries) and their related vendors.
• Review list of approved Quality Documents to identify audience assignment and maintains the QD Training Matrices up-to-date. Manage requests for appropriate training assignments in due time in the Learning Management System (LMS) e.g. training courses, curriculum, users etc.
• Contribute to Quality Control (QC) strategy and perform QC on training activities.
• Manage requests to provide training status on QD's training for PV associates. Manage the training mailbox to ensure that customer requests are answered on due time.
• Manage the electronic binder to allow that all PV associates have available CV and Job-description up-to-date for audit or inspection requests.
• Coordinate activities with the Training service provider including follow-up meetings. Contribute to the preparation of Training metrics and Key Performance Indicators.
• Support inspections and audits by providing required data on due time, participating to interviews, contributing to root cause analysis and CAPA proposal.
• Collaborate with the Training network with associates from other functions.
• Coordinate or participate to specific projects related to PV or quality process or tools improvements. Contribute to GxP non-QD training for Medical (Instructor-led training, e-learning courses....)

• Experience in Training system management
• Experience in GxP Quality system management
• Experience in Pharmacovigilance and/or Medical
• Knowledge in International Pharmaceutical Regulation e.g. GVP, GCP, ICH
• 5-7 years of Experience in relevant industry

• Pharmacovigilance
• Quality systems
• Medical Writing
• Electronic Data Management System (EDMS)
• Quality Risk Management
• Project management skills
• Use and develop Dashboards

• Bachelor's degree in a science field, examples: Biology or Health Science degree, Bachelor of nursing degree

• good level of Professional English