Minőségbiztosítás állások Külföldön főiskolai végzettséggel

• Prepare and submit approval dossiers, ensuring compliance with deadlines and budgets
• Obtain and maintain international approvals (e.g., VDE, UL, CCC) and ensure CE conformity
• Manage and update standards and approvals in the relevant databases

Together with the senior manager of your stream, you will take on a moderating role, understanding and mastering the individual processes, in order to moderate between the ZEISS functions and process experts in a goal-oriented manner...

• Develop scale-up primary manufacturing processes based on fundamental identified criterias
• Define design elements from the process requirements
• Set key aspects the process must meet for installation at the Product Technology Center & JTI factories

• Develop scale-up primary manufacturing processes based on fundamental identified criterias
• Define design elements from the process requirements
• Set key aspects the process must meet for installation at the Product Technology Center & JTI factories

• Manage the development of industrial processes for new products or improvements.
• Oversee manufacturing risk assessment activities.
• Define strategies and action plans.
• Organize test execution and ensure the completion and follow-up of studies, trial batches, and process validations.

• Maintain a comprehensive register of all rework, retrofit, and modification activities for the BOXER vehicle and its variants.
• Track progress of open rework/retrofit tasks with industrial partners and suppliers, ensuring clear status visibility at all times.

• Performing manufacturing and quality control testing of semi-finished and finished products in compliance with regulatory requirements (ISO 13485)
• Conducting analytical release of QC results
• Applying your expertise in Next Generation Sequencing (NGS) within QC workflows

• Management of deviations, change requests as well as corrective actions and preventive actions
• Review of equipment qualifications, batch documentation, and product release preparations for clinical studies

• Supervise and support on-site quality assurance, addressing technical non-conformities and ensuring compliance with change management protocols
• Coordinate with Supply Management for the Quality Gate 1 and incoming goods inspections

• Moderation, creation, and updating of design and process FMEA
• Creation and maintenance of control plans and inspection characteristics
• Conducting first article inspections and sample approval
• Planning and supervision of measurement system analyses and calibrations
• Conducting quality training courses

• Guiding and supporting your team by overcoming roadblocks and exceeding expectations
• Ensuring appropriate staffing for all active Simultaneous Development Teams (SDTs) in collaboration with Program Management and Quality leadership

• Coordinate SICPA's IMS activities across more than 20 sites worldwide.
• Maintain and control process mapping and system documentation, ensuring accuracy and compliance with quality standards.

• Implement and maintain quality procedures in accordance with ISO
• Lead or support internal audits.
• Manage and drive the internal non-conformities process until issues resolutions.
• Manage Non conform product segregation and containment actions.