Trabajo de Senior Quality Assurance Specialist (Hybrid)


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Who we want: • Detail-oriented process improvers. Critical thinkers who naturally see opportunities to develop and optimize work processes – finding ways to simplify, standardize and automate. • Strategic thinkers. People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities. • Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions. • Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues • Curious learners. People who seek out cutting-edge research and information to expand and enhance their ability to be ready for what’s next.(What you will do: • Provides support in the tasks related to Product Registration, Regulatory Affairs & Quality Assurance (including audit processes). Collaborates in the execution of the processes that guarantee fulfillment of these. • Act in compliance with the Stryker code of conduct, laws, regulations and standards applicable in Argentina & Uruguay. • Ensure that the authorization licenses for Stryker Argentina activities are maintained. • Responsible to ensure document accuracy of information submitted before the Health authority. • Contact with Competent Authority for the imported and distributed products & company activities. • 1.- Compliance • All business and related matters must be conducted in accordance with all laws and regulations, including the Foreign Corrupt Practices Act (FCPA), the Stryker Code of Conduct, and to the highest ethical standards. • 2. Quality Assurance • • Take the necessary actions for the maintenance and monitoring of the Quality Management System, and its adequacy to the current regulations to be required. • • Manage Complaints & CAPAs, including contact with Surgical Technicians • • Analyze data to identify potential nonconformities and improvement opportunities • • Monitoring and optimization of Service Indicators • Define and implement the Internal / External Audit Program. Conduct enabling site visits and monitoring storage conditions of distributors and direct customers, where required • • Define and Implement the Audit Program for Suppliers and Distributors • • Align and maintain updated local procedures according to corporate documents. • • Control of changes • • Verification, release of products and their traceability. • • Maintenance and monitoring of databases and process KPIs • • Maintain and / or achieve the different certifications required by the company • Receive, report and track complaints responses generated by product quality, using Stryker tools designed for this purpose (CHS – TrackWise) • Follow up, communication and timely report of products involved in quality quarantines (Hold) utilizing applicable Stryker PMS systems • Coordinate needed activities for launching, implementation and closing of field safety corrective actions (FSCA) utilizing applicable Stryker PMS systems. • Prepare input information required and track the proper QMS management reviews implementation. • Define and implement training programs, creating awareness through the organization members on the importance and commitment to the QMS, different QMS processes. • Manage and obtain Product Quality Certificates of Analysis issued by the manufacturers where applicable • Check the timely and correct identification and disposal of the product returned by customers, quarantine and non-compliant. • 3. Regulatory Affair • •Responsible for the management of documentation and local coordination for compliance with the annual product registration plan • • Responsible for taking the regulatory actions related to the renewals, maintenance and updating of the product records according to the notifications of change sent by the manufacturers. • • Contact with Competent before the Health Authority with legal responsability for the imported and distributed products • • Maintenance and monitoring of databases and KPIs • • Support to the different areas in specific tasks. • Follow up and communicate to commercial teams about regulatory status and registration progress on current and new devices for the Styrker Argentina business. • Responsible the following activites: • Use of the GPRD process and available Stryker databases to obtaining technical and legal documentation required for the completion of registration dossiers for regulatory filling • Prepare and submit answers to the health authority requirements on registration dossiers on process in a timely manner in accordance the regulatory requirements • Obtain, prepare, submit and track the product samples when required by regulatory authorities through registration processes. • Accurately track and update and maintain databases of registration records and health approval • Maintain a registration renewal process in line with regulatory requirements • Review and comment on the regulatory impact of device changes and communicated through Stryker Change notification processes • Measure and report metrics on regulatory filings submission and approval. • Manage the regulatory requirements for local medical devices labeling and partner with the operations and distributors to complete any required local labelingWhat you will need: • Academic degree in Pharmacy. • Previous experience in Quality Assurance • Intermediate English (reading and writing). • Health regulation in force for medical devices is a plus • At least 1 year with active participation in Trade Associations and relationships with Health Authorities is desired • ISO 9001/13485 Internal-Leader Auditor is desired. • Experience at the Medical Devices Industry is a plus#LI-LatAM

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