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Description du poste:
Description
· Support Central regional organization to ensure the maintenance of the Quality Systems as per (COMPANY NAME) Quality Standards, ISO 9001 Standard and established quality goals
· Ensure efficient information flow and effective communication of all relevant quality matters
· Establish corrective action & preventive actions to mitigate potential or actual noncompliance
· Support Supplier/Distributor Monitoring Program, as applicable;
· Manage the Training Program, as applicable;
· Manage the Field Actions and Product Complaints Management Program, as applicable;
· Record and manage quality issues, escalating serious events to senior management;
· Support hosting and managing of internal and external audits and inspections;
· Support creating inputs for management review process and quality planning;
· Participate in local and regional quality/compliance projects.
Qualifications
* Bachelor's degree in bioscience, engineering, or business.
* Working experience in the Medical Device Industry in quality/regulatory function.
* Strong collaboration skills and ability to build partnerships internally and externally.
* Excellent written and oral English communication skills.
* Advanced computer skills in MS Office
Origine: | Site web de l'entreprise |
Publié: | 09 Sep 2023 |
Secteur: | Santé |
Langues: | Anglais |
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