Minőségmérnök állások, munkák

A Minőségbiztosítási Igazgatóság előadói munkakörbe keres munkatársat a Helyes Gyógyszergyártási Gyakorlat (GMP) feladatok ellátására ...

Establish and maintain a project-specific Quality Management System (QMS) Develop and continuously improve the Quality Management Plan, including process maps and action plans Conduct quality assurance activities, including gate reviews and weakness analyses Support change management processes from...

Write, review and approve design and development documents, including design inputs, outputs, verification, validation, and design transfer activities...

• Test 3D visualization, animation, and drone choreography features
• Validate flight path generation, collision detection, and show simulations
• Propose new features based on creative workflow insights
• Document bugs and verify fixes
• Test import/export from various 3D formats and modeling programs

Write and maintain clean, reusable, high-quality scripts that test product functionality automatically Contributing to bug finding and error reporting Contributing to the continuous improvement of automation frameworks/tools Preparing detailed test reports Take part in brainstorming to come up with...

• Perform supplier control and management activities
• Prepare and execute various studies and reports
• Support the risk management process and associated documentation applicable to STAAR Surgical AG
• Initiate and lead project teams on Corrective Action/Preventive Action (CAPA) projects

• 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)

Proactively develop and implement the quality strategy for the assigned components group, aligning it with long-term business goals and engaging with cross-functional stakeholders globally....

• Batch record review for API and bulk product for monoclonal antibody prefilled syringes
• Assessment and documentation of product deviations, OOS, and changes
• Quality oversight for relevant service providers, including CMO's, laboratories, technical operations and supply chain

termelő területek minőségügyi támogatása a gyártási folyamatok és dokumentálások felügyelete; műszaki változások nyomon követése vevői és beszállítói minőséggel kapcsolatos dokumentációk kezelése és nyomon követése hibaanalízisek, kiértékelések elvégzése, a kiértékelési rendszer felülvizsgálata és...

Design and write automated test cases Expand test automation coverage Close collaboration with developers and product team Independent test case planning and implementation...

• Maintain and further develop our QMS in line with EN ISO 13485 and MDSAP
• Create, update, and improve procedures, forms, and training materials
• Plan and deliver training on procedures and regulatory requirements
• Lead and oversee CAPA initiation, processing, tracking, and review

Címkék, feliratok előkészítése, felragasztása a termékekre. Minőségellenőr munkatárs napi munkájának támogatása. Raktár terület napi szintű takarítása, a használt tisztítószerekre vonatkozó előírások és higiéniai elvárások betartásával. Berendezések tisztítása, beállítása, kisebb karbantartási...

• Creation of the IVP (Integration & Verification Plan) for L2 and L3
• Creation of the IV verification strategy and assignment of M0C (Means of Compliance) to functional requirements (DesVerActions and ProdVerActions DOORS modules)

• Develop and implement local quality procedures and work instructions to align with contractual requirements, local standards, and Quality Management System (QMS).
• Conduct internal and external quality audits and reviews.

You develop, maintain, and continuously improve the Quality Management System in accordance with ISO 13485, MDR, and other applicable regulatory requirements...

• Develop and maintain automated tests: automate when it makes sense, think about ROI, don't overengineer solutions.
• Own the testing and quality processes of the team
• Improve the development process
• Lead the QAs of the hardware development unit
• Maintain and improve the testing infrastructure

• Lead global manufacturing quality strategy, ensuring alignment with Voith Hydro's renewable energy objectives.
• Ensure quality oversight across diverse manufacturing processes, with a strong focus on turbine and generator fabrication.

• Review customer specifications and legal/statutory requirements, ensuring compliance with Voith Hydro standards and EQM guidelines.
• Prepare and issue project-specific Quality Plans and documentation (e.g., Inspection & Test Plans, QS, MGS).