
Design Control Engineer IRC268542
- Slovensko
- Trvalý pracovný pomer
- Plný úväzok
- At least 4-5 years of quality management work experience.
- Knowledge and understanding of ISO 9001 series and ISO 13485 standards.
- Knowledge and understanding of regulations on medical device manufacturing (at least US FDA Regulations).
- Knowledge of the software development life cycle (work experience in software development or knowledge of the international standards that regulate this process such as IEC 62304 standard).
- Experience with Software Risk Management (ISO 14971) is a big plus.
- Fundamentals of software testing and quality assurance.
- Fundamentals of FTA/FMEA/FMECA methodologies.
- Knowledge of the QMS structure.
- Experience of participation in internal and external audits.
- Strong documentation management skills.
- Ability to work with standards. Ability to comprehend a new document with standards, analyze it well enough to assess the standards’ value/benefit for the Company against possible risks entailed.
- English at the upper intermediate level.
- Presentation and training skills.
- Ability to coordinate and lead meetings in a team and with other participants.
- Establish process and documentation to validate the Test Automation Framework and Scripts in compliance with Client’s SOPs (SW SOP, CSV SOP etc.)
- Create the validation plan and drive the GL Test Automation team to follow those processes and create corresponding documentation/deliverables.
- Review GL generated deliverables to ensure accuracy and completeness.
- Work with Client’s QA and Leads for approvals of deliverables.