€ 70,000 - € 90,000
Detachering via YER
Medical & Health
Over deze vacature
In this role, you have the opportunity to:
Guide and support Business Groups, Markets and enabling functions to- “always do the right thing”. This involves being a confident advisor on approval, regulatory compliance and quality management related topics, in order to achieve timely releases of innovative products that deliver high quality and outstanding reliability to the lives they will improve.
- Maintain and manage QMS processes for quality, compliance, and effectiveness. Review and update QMS procedures, support inspection and audit activity, responsible for QMS process areas as assigned;
- Perform gap assessments, develop and manage quality plans, provide metrics and status reports as appropriate;
- Ensure the product team follows the QMS throughout the product lifecycle, coaching and mentoring the team for QMS activity as well as actively participating as the project qe;
- Provides effective oversight of all design related activities during the product lifecycle, including compliance planning;
- Participate in product planning, requirements development, criteria establishment, design reviews and DHF reviews;
- Assists with FMEA, risk management and development efforts with quality tools and investigations;
- Review test and performance data, perform complex root-cause analysis, drives improvement and remediation activity with the development team;
- Use post-market analytics and statistics to report on product performance in the field (provide feedback to manufacturing, suppliers or design teams) and initiate field actions when required. Analyze and review product quality issues/trending, driving continuous improvement;
- Lead supplier management activity, including: supplier metric reviews, complaints, trend analysis, supplier audits, author and review supplier quality agreements, maintain the ASL, initiate and manage SCARs, capture and report metrics as appropriate;
- CAPA process management activity, including any of: scheduling and conducting CRB, assisting CAPA owners to keep CAPA content compliant and activity on-schedule, own Q&R CAPAs, capture and report metrics as appropriate.
With a growing presence in cardiology, oncology, and women's health, Philips operates in the areas of Imaging Systems, Patient Care & Clinical Informatics, Home Healthcare and Customer Services. Philips combines its clinical expertise and human insights to create innovative solutions across the continuum of care, in partnership with clinicians and our customers, to provide better value and expand access to care for millions. Our teams are working hard every day to improve patient outcomes all the way from disease prevention and screening to diagnosis, treatment, therapy monitoring, and disease management. Irrespective of whether the care cycle takes the patient from doctor's office to hospital or hospital to home, or simply from one medical department to another, Philips Healthcare's unique medical solutions are designed to optimize the quality and flow of patient information and clinical decision making.
We welcome you to a challenging, innovative environment with great opportunities for you to explore. YER is preferred supplier. You will be employed by YER and seconded to Philips.
Our benefits are very competitive and designed around your preferences:
- A competitive salary depending on experience
- Extensive set of tools to drive your career, such as a personal development budget, training and coaching
- Healthy work-life balance
We are looking for:
A person who is excited by the unique professional challenges presented by our Tele-health products, has strong technical competencies, and demonstrates resilience in challenging situations. We are looking for a perfectionist- a fixer who continuously strives for excellence as a way of life; not just as a job. We’re looking for someone who can inspire others to adopt this mentality of prioritizing quality above all else, in a relentless pursuit to improve the quality of life for the billions of people Philips brand touches each year.
To succeed in this role, you should have the following skills and experience:
- Bachelor’s degree in Computer Science, Engineering or related disciplines;
- Minimum of 5+ years’ experience in Quality Engineering in an FDA regulated, ISO 13485 QMS, Medical software or systems, product environment;
- CAPA’s, FMEA, Risk Management, Root Cause Analysis, Troubleshooting;
- Design Review/Controls;
- Competency working with requirements of FDA 21 CFR Part 820, ISO 13485, ISO 62304;
- FDA Inspection and Internal and External Audit Support;
- Design Verification/Validation;
- Working knowledge of appropriate global regulations, requirements, and standards;
- Data Analysis, Trend Analysis
While not required, the following skills are preferred:
- Experience with Software Agile Methodology;
- Experience working with suppliers/vendors;
- ASQ Certified Quality Engineer (CQE);
- Six Sigma Green Belt / Black Belt;
- MDD/EU MDR.