Architect and engineer állás, munka

• Develop, implement and maintain an effective compliance program ensuring adherence to pharmaceutical regulations and standards
• Maintain systems to identify, track and mitigate compliance and quality risks while ensuring continuous inspection readiness

• Improving and maintaining QA related processes in VS
• Ensuring alignment with ISO 9001, ISO 13485, FDA and Coloplast Quality Management System
• Creating, implementing QA related documents
• Preparing systems for ISO / FDA and internal audits
• Organizing QA trainings

• Initiate, communicate and process claims from incoming material and assembly towards supplier.
• Track 8D reports and realize 8D reporting towards the local Quality Management on plant level as well as the regional Supplier Quality Assurance organization.

• Managing the process of registering internal and external energy efficiency projects to handle all efficiency initiatives in one central framework.
• Review all internal and external projects to determine Energy Efficiency, EEOS in group level.

• Take responsibility for manufacturing and production quality assurance processes, ensuring standards are not only met but consistently exceeded
• Conduct process audits to ensure compliance with industry and customer requirements

• Minőségbiztosítás a jelenlegi folyamatokban
• Erős ismeretek a következő rendszerekben: ISO 9001 / TS 16949
• A jelenlegi folyamatok folyamatos optimalizálása
• A bejövő áru ellenőrzés és a kimenő áru ellenőrzés folyamatának felügyelete, ellenőrzése
• Együttműködés a vevői/szállítói minőségügyi szervezetekkel

• Az Ön szerepe – rendszerek működtetése, fejlesztése és egységesítése 4 gyártóhelyen:
• A vállalat minőségirányítási rendszerének működtetése, folyamatos fejlesztése.
• Gyártási folyamatok nyomon követése a nyersanyagátvételtől a késztermékig.

• Provide product care and hardware improvements for existing products through continuous refinement and the introduction of innovative technology solutions
• Coordinate and manage suppliers of third-party electronics manufacturers, ensuring product quality and compliance

In this expert role, you will be instrumental in the strategic development and implementation of future-oriented BEOL process flows...

• 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.