About the role:
Guarantee quality compliance of processes and products associated with suppliers. Ensure that products are manufactured and delivered to ZimVie according to the established quality standards.
What you'll be doing:
Select and coordinate the supplier lifecycle management since the initial selection and qualification, monitoring and feedback.
Management of the Supplier Production Process Approvals including definition of control plans and process/product validations.
Coordination and execution of the Supplier Corrective Actions Report
Carry out external audits and participate in the internal audits of the Quality System.
Support the supplier validation activities of facilities, equipment, processes and computer systems as established in the internal procedures of the Quality System.
Provide support in the management of Health Hazard Evaluations (HHE) and Health Hazard Evaluation Determination (HHED), Product Holds (internal/external) and product quarantines.
Management of production transfer projects (Transfer vendor to vendor).
Make modifications and updates to Biomet 3i Dental Ibérica documents as a result of the implementation of corporate procedures or other changes.
Develop, modify and implement Supplier Quality procedures, systems, processes, and metrics to drive standardization and common practices across the supplier network.
Evaluate the conformity of dental purchased products manufactured in Biomet 3i Dental Ibérica when requested by the legal manufacturer.
Manage New Product Introduction and/or new industrialization projects associated with suppliers.
Participate or Lead OPPs (Operating Project Plan) and improvement projects.
Manage product and process non-conformities for purchased products.
Management of measurement and control equipment out of specifications according to internal procedures.
Select appropriate measuring equipment to carry out the inspection of the manufactured product.
Write and execute TMVs (Test Method Validation).
Prepare monthly indicators related to Supplier Quality activities.
Management of incoming inspection sheets.
Management of the Supplier Change Notifications.
What you'll need:
Be in possession of a university degree in Engineering or similar. Postgraduate degree in Quality Management or similar is desirable.
It is desirable to have at least 2-3 years of experience in a productive and multinational environment.
Possess a high level of English, both spoken and written.
It is essential to have knowledge in the use of office tools, especially Excel, as well as data analytics (Power BI). Furthermore, the use of ERP systems, especially Oracle, is essential.
Knowledge of statistics associated with process control and sampling plans.
It is desirable to have knowledge about the operation of a Quality System and the international regulations applicable to the business sector, such as ISO 9001/13485 or 21 CFR 820 regulations.
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