Quality Systems Engineering Supervisor (Maternity Cover)At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.
Job OverviewThe Senior Quality System Engineer is a member of the Quality Systems department. They are responsible for supporting and leading the organization in its drive towards optimum quality compliance to site as well as corporate policies and external regulations, while adhering to efficient and lean principles. This role is responsible for working with the wider organization to ensure the effective and compliant implementation of the site Quality Management System and to prepare the site to demonstrate compliance during regulatory audits. The role will also work across-site to lead and implement projects that will transform the operating practices and systems of this Quality Management System.
This is a 12 month contract for maternity cover.
Job Responsibilities:Stay current with quality system standards and requirements.Provide Quality Systems support for the Galway site.Provide supervision to different subsystems such as Document Control, Training and QS Technicians.Frequently interact with other supervisors and/or peers.Assist in the preparation and maintenance of records associated with the management review process.Develop effective quality metrics and communicate the results to key stakeholders using reports, presentations, and dashboards.Ensure compliance and drive improvements in QS processes.Participate in Quality Systems projects under the direction of the Quality Systems Manager and/or Head of Quality.Develop and implement processes, procedures, and instruction to sustain and improve the Quality Management System.Support Quality Systems Manager in the development and implementation of quality systems strategies and objectives.Coach and mentor when needed.Work within cross-site teams to implement best practices in methods and systems that drive Quality Excellence within the Quality Systems team on best practice.Lead and maintain Cross-training efforts within QS organization.This is not an exhaustive list of duties or functions and may not necessarily comprise all the essential functions.Qualifications:Bachelor's degree or local equivalent in Engineering / Science / Quality field. Master's degree or higher or local equivalent may be preferred at this level.A minimum of 5 years of progressively responsible professional level experience. Previous experience at Senior/Supervisory level within the Medical Device or related industry may be preferred.Key Requirements:Must be familiar with all aspects and elements of a quality system, ISO13485; FDA QSR & MDSAP.Must have experience of hosting audits from external regulatory agencies and corporate functions.Experience for leading cross-functional teams would be a benefit.Demonstrates ownership for the integrity of work.Ability to work independently under general guidelines and supervision and consider options for completing work.Strong written and verbal communication skills.Proven ability to influence.Excellent attention to detail.Highly organized with strong ability to prioritize tasks and work on own initiative.Trained Auditor ideally lead auditor training and/or experience.Effective interpersonal skills as demonstrated through prior supervisory experience.Ability to adapt to changing duties and responsibilities.Core Values: Integrity, Accountability, Teamwork, Innovation, Inclusion.
We are an Equal Opportunities Employer.
CompetenciesMotivating Others, Managing and Measuring Work, Building Effective Teams.
Location: GALWAY, G, IE, H91 VN2T
City: GALWAY
State: G
Country/Region: IE
Travel: None
Requisition ID: 123267
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