Sqa mérnök állások, munkák Külföldön

• Fémes minták szakítóvizsgálata Zwick gépeken
• Romboló anyagvizsgálatok elvégzése laboratóriumi környezetben
• Vizsgálatok dokumentálása, jegyzőkönyvek készítése
• Munkavégzés szabványok és eljárási utasítások szerint

Coordination & Execution of Test & Qualification Activities for ElevatorsYou will be responsible for overseeing and conducting test and qualification activities for component as well as full elevator system tests within our Rottweil test tower....

• Set up test systems (hardware / virtualized) in complex network structures so that they are ready to perform test cases
• Set up and run tests in line with test specifications and take appropriate actions (i.e. passing the test, raising a defect)

• Review automatically generated videos for linguistic accuracy, visual consistency, and content quality
• Perform quality assurance and editing using AI-driven platforms such as Heygen or Synthesia
• Identify and correct errors in text, audio, and visual presentation

• Review automatically generated videos for linguistic accuracy, visual consistency, and content quality
• Perform quality assurance and editing using AI-driven platforms such as Heygen or Synthesia
• Identify and correct errors in text, audio, and visual presentation

• 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

Following up on production-related nonconformities, supporting root cause analyses, defining and monitoring corrective actions, and preparing evaluations and statistics of nonconformities...

PURPOSE - The purpose of the role is to represent the Quality department in transport projects by: - Guaranteeing methodological rigor in the development plan and coordinating all qualities activities within the project teams.   TASKS AND RESPONSABILITIES - Ensure that development standards are...

• Perform daily business in technical and administrative aspects
• Support Production (Shift) Team Leaders to ensure appropriate skill level of production and SCM teams in all quality-related process aspects

• Strategic quality assurance, review of Q requirements and auditing of suppliers
• Carrying out internal product tests and inspections
• Responsibility and assurance of delivery quality
• Evaluation, monitoring and situational development of existing and potential new suppliers

Management of regional and local Quality & HSE Team and activities as well as implementation of group-wide initiatives and projects, including qualification and personnel development...

• 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

• Planning and initiation of business cases, definition of the project scope, objectives and deliverables. This includes gathering requirements, assessing feasibility and developing a project plan that aligns with organizational goals
• Monitoring of timelines and budget

Prepare, support the creation and review and execute the release of all technical documentation for digital health and software products ensuring compliance with applicable standards and regulatory requirements such as IEC, IEC...

• Maintaining and continuous improvement of the Quality System, including the associated management documentation and ISO certifications
• Planning and coordination of internal audits as per Internal Audit Plan
• Planning and coordination of the yearly Management Reviews including Reporting

• Take part in the definition of quality objectives for suppliers and supplier management
• Conduct quality audits at suppliers and service providers
• Support Purchasing in supplier selection.

• Acting as a key contact to IEE customers for quality-relevant topics during development and serial production
• Handling customer complaints
• Organizing and following up of customer audits
• Minimizing quality risks
• Preventing field actions
• Minimizing warranty costs and scrap costs

• Developing and maintaining sterility assurance and contamination control strategies for aseptic processing
• Leading risk assessments for aseptic process, single use systems and critical interventions, and ensuring compliance with authorities relevant Guidance such as Annex 1