.Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care.
With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring.
Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs.
Convatec's revenues in 2023 were over $2 billion.
The company is a constituent of the FTSE 100 Index (LSE:CTEC).
To learn more about Convatec, please visit www.Convatecgroup.ComPurpose of the function/position:The inspections and the adequate planning and documentation.Notify and follow up on problems found in processes, products and materials.Analysis on documentation of the area to be updated in accordance of planned changes/projects.Responsibilities:System:To assist to Senior Quality Control Engineer in the implementation of the requirements into the QA System to ISO 13485 Standard & FDA CGMP Quality System Regulation.To assist in to carry out internal audits when this is required.To provide or assist in Quality Assurance Training programs.To follow up all work instructions and quality records.To provide collections and keeping of quality records of the area.To comply with the company quality policy.Leadership & Inspections:To supervise the activities of the Quality Inspectors / QC leader.To evaluate the necessary resources to perform the task inspections and release the material in a correct way meet with the deliveries on time (resources, equipment, etc.
).To evaluate that the established systems are running in a right way.To evaluate the plans of inspection and test method from the processes in order to improve them or simplify apply.Assure that the Q.C.
personnel have the proper training to perform the activities of the area.Responsible for the coordination of personnel for the adequate planning on the product inspections also on participation on special activities as the reworks/reinspection, validation process tests, product and process changes, special records, measurements, investigations, etc.
if this is required.Disposition of material/products:Responsible for control of the materials in detention in the quarantine of the clean room.Responsible for the follow up and final disposition of subassemblies and final product (no conformance, acceptable materials, etc.)
in adequate time.Support to Supplier Quality Supervisor on the raw material disposition, when required.Support to Process Quality Engineer for monitoring or failure analysis, when required.Release of final products:Responsible for the release of final product that fulfill with quality specifications and adequate records in accordance with the Quality System