Description:
As Design Assurance Engineer, you will drive the subject matter expertise of our Design Control process, as well as our Risk Management process to support the product documentation during all phases of NPD projects and review essential parts of the technical documentation. You will be part of our global Quality organisation with a strong professionally foundation.
Key Responsibilities:
Within one or more product development projects or remediation projects you will be:
- driving adherence to the design control as well as risk management processes in product development projects
- a key figure in the planning and follow-up of all design control activities.
- involved in all project activities, through review and approval to ensure compliance to our standard operating procedures and instructions as well as external standards and regulations.
- involved in assessing, developing, and continuously improving the standard operating procedures, instructions, and templates, in the context of risk management and product development.
Skills & Experience:
You bring extensive experience from a similar role as Design Control Engineer or Product Quality Engineer, in new product development or in remediation, driving the design control activities within a Medical Device company. You may have worked in a maintenance of Quality Management System (QMS) process’s role, looking after the process, as well as technical documentation preparation.
To be truly successful in this position,
- you understand that key contributing factors to success are, cooperation and building strong collaboration with other functions, like Global Quality, R&D, RA, Process Engineering and Production
- You communicate easily to achieve a common goal and at the same time deliver high quality and timely solutions and deliverables.
- You appreciate thoroughness and correctness as a natural focus of the daily work.
- Working in a dynamic environment, you know how to drive and follow up on the cross-functional team’s contributions to the design control documentation, prioritizing your tasks to meet the agreed project timelines and adherence to the process.
Qualifications/Education:
- You hold a master’s or bachelor’s degree in engineering, pharmacy, technical science, or similar technical diploma in laboratory science.
- Proven 1-2 years experiences as Design Assurance Engineer or similar
- Preferably experience with maintenance and development of QMS processes or design control processes within new product development in Medical Device context
- Hands-on experience with Design Control in accordance with EU ISO 13485, US 21CFR820, ISO 14971 and MDR
- Experience with requirements engineering, product risk management, and usability engineering
- Knowledge within regulatory legislation and standards
- Preferable knowledge within in Medical Device product development (Class II)