working in the QA RA Department of this medical device company. AREAS OF RESPONSIBILITY KPI DATA COLLECTION and trending remarks. MEDICAL DEVICE FILE Managing the Group Medical Device File programmes and databases Quality Documents. Training Ensure assigned training is completed timeously. Provide training on areas under
working in the QA RA Department of this medical device company. AREAS OF RESPONSIBILITY KPI DATA COLLECTION and trending remarks. MEDICAL DEVICE FILE Managing the Group Medical Device File programmes and databases Quality Documents. Training Ensure assigned training is completed timeously. Provide training on areas under
and trending remarks MEDICAL DEVICE FILE Managing the Group Medical Device File programs and databases Quality Documents Training Ensure assigned training is completed timeously. Provide training on areas under
and trending remarks MEDICAL DEVICE FILE Managing the Group Medical Device File programs and databases Quality Documents Training Ensure assigned training is completed timeously. Provide training on areas under
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MEDICAL DEVICE FILE
Managing the Group Medical Device File programs and databases
Documents
Training
Ensure assigned training is completed timeously.
Provide training on areas
directories. Device Management Extraordinaire: From SCCM to Microsoft Intune, you've got device management management down to an art. Virtual Device Management Whiz: Master virtual environments with Horizon, Citrix, Working Model (AWM) Duties: Daily monitoring of device management environments Be responsible for the
Directory/Azure Active Directory
to local regulations. Pharmacovigilance-Safety training support: Support LSO/CSTL in the preparation, and timely documentation of Pharmacovigilance training for Local Operating Company employees, and Adverse Event and Product Quality Complaints (AE/PQC) training to distributors/3rd-Party vendors and with the implementation, including Local Safety Unit (LSU) training and adherence to PVAs, Coordinate the provision (for drugs non-medicinal products & Medical Devices in the scope of responsibilities), evaluation of
to local regulations. Pharmacovigilance-Safety training support: Support LSO/CSTL in the preparation, and timely documentation of Pharmacovigilance training for Local Operating Company employees, and Adverse Event and Product Quality Complaints (AE/PQC) training to distributors/3rd-Party vendors and with the implementation, including Local Safety Unit (LSU) training and adherence to PVAs, Coordinate the provision (for drugs non-medicinal products & Medical Devices in the scope of responsibilities), evaluation of
including complementary medicines and medical devices for end-to-end regulatory activities.