QUALITY ENGINEER MANAGER - BIOMEDICAL COMPANY
Descrizione dell'offerta di lavoro
Bullet points great growth opportunity multinational company il nostro cliente biomedical company la figura ricercata reports to the group general quality manager, the quality engineering manager will be accountable and responsible for product quality within different production plants (including plastic moulding, assembly in cleanrooms iso-8) and outsourced activities such as extrusion with different materials including silicone. leads a team of quality engineers, technicians to effectively monitor processes, identify and correct issues, and continuously improve the area using problem solving tools and metrics. partners closely with production manager, manufacturing engineering, suppliers and project leaders to drive continuous improvement in quality, cost, and delivery on commercial products and to ensure new products are implemented with key process controls and product checks in place using business improvement methodologies such as kaizen, lean, six sigma models. main responsabilities: guide, coach, direct, and develop direct reports, and drive best practices throughout the organization; develop a workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives; works with key partners, integrate business & group priorities, plans resource allocation accordingly; works cross-functionally in identifying and resolving technical issues. contribute to solving technical problems by coordinating and facilitating sessions in collaboration with the various stakeholders; develops, provides guidance, and deploys quality strategies and approaches; key partner in developing and implementing all department and site strategies; establish proper processes and metrix including performance indicators to monitors and drives department progress against goals and objectives; collaborate with the quality system & regulatory team to ensure compliance with company policies & medical devices standards/laws; participate to new product development programs particularly design transfers / change management activities; manage failure investigations related to potential field performance issues of product; owns and manages quality discrepancies related to process and product; develops scope, disposition, and corrective actions for prevention of future discrepancies; monitor corrective and preventive actions (internal and external) with the managers and provide them with the necessary support to ensure that corrective measures put in place are effective. il candidato prescelto bachelor's degree (business, engineering, a technical field or equivalent) 7+ years of experience in working in quality assurance related area which should include 2-3 years of supervisory experience required. experience working in a regulated industry (medical device, pharma, aerospace, etc) solid knowledge of quality system principle such as iso , iso, cfr820. business improvement methodologies such as kaizen, lean, six sigma models certification preferred auditing experience preferred experience with performing root cause analysis, change control and validations (iq, oq,pq) is preferred. leadership, initiative and accountability; impact and influence; rigorous excellent computer skills including word, excel, power point and visio experience in preparing data and charts for management excellent organizational skills, analytical abilities, and ability to multi-task occasional domestic travel required fluent in italian and english both written and spoken. cosa comprende l'offerta great growth opportunity note fai click sul comando “candidati”. la ricerca sarà svolta da un consulente di pagegroup. pagegroup in italia è formato da michael page international s.r.l. e da page personnel italia s.p.a.
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