Quality Director, Medical Devices
Philips, Farnborough, Hampshire
Quality Director, Medical Devices
Salary not available. View on company website.
Philips, Farnborough, Hampshire
- Full time
- Permanent
- Onsite working
Posted 1 day ago, 3 Nov | Get your application in today.
Closing date: Closing date not specified
job Ref: 65a7365d500b4d8e88c89c80f6a92094
Full Job Description
- As the Director of Quality for EC Pro you will deliver proactive quality excellence through improved customer experience and regulatory compliance across FDA Class I, II and III medical devices and various global competent authorities.
- You will have end to end quality responsibility and lead on product design (sustaining & improvement); supplier selection & qualification including APQP; post market surveillance; customer service; procurement; QMS management; quality key performance indicators all the while assuring products are both safe & effective and compliant with business quality.
- This role will oversee a portfolio of quality related projects and programs, alongside accountability for quality challenges and internal/external auditing
- This is a complex, matrix environment where you will have a solid line report to the Head of Quality for Emergency Care Business and a dotted line to the EC Pro Business Category Leader. As Director of Quality, you will be a key member of the Business Management Team representing quality functions to drive continuous improvement and lead direct and indirect reporting lines.
- From competitive salary, company car allowance and performance bonus to family friendly policies, flexible benefits and access to Philips University, a career at Philips comes with all sorts of wonderful benefits. Be sure to speak to your recruiter about all the benefits on offer. How we work together
- We believe that we are better together than apart. For the role, this means working in-person at least 3 days per week in our Farnborough, Hampshire office.
You are a seasoned Quality Leader able to use resourcefulness and strategic thinking to navigate complex multi-site, matrix environment to deliver project and ensure a thriving quality team. - Your background is in Medical Devices (Class I, II, and III products) with FDA and other worldwide standards/regulations experience.
- You have end to end quality management experience (Design, development, contract manufacturing, post market surveillance & QMS) with teh ability to oversee and connect all elements
- You have the confidence to operate independently, make decisions and find solutions to overcome challenges.
- You are approachable with strong relationship building capability.
- You are educated to Bachelor degree level (Science, Engineering, or similar technical discipline), or have acquired equivalent experience.
If you're interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here . About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. - Learn more about our business here
- Discover our rich and exciting historyhere
- Learn more about our purpose here About Philips UKI In the UK, we are recognised as a Disability Confident employer and are proud to be part of the Armed Forces Covenant & Mental Health at Work Commitment. We welcome all applicants including those from minority backgrounds, LGBTQIA+ and individuals living with a disability. Because we are at our best when you are, you can safely share any reasonable tools or adjustments needed during our recruitment process and beyond. For more information, read our Inclusion and Diversity Policy and, to know more about your Human Rights, we encourage you to view this report.