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Philips QA Engineer in Chichester, United Kingdom


In this role, you have the opportunity to provide Quality Systems Engineering support to the Respironics Drug Delivery (RDD) organisation to ensure that products, processes and projects are in compliance with the Quality Management System, Philips Policies and Quality System regulations.

You are responsible for

  • Conducting quality systems’ audits in support of departmental needs

  • Leading and mentoring cross functional teams with the implementation of appropriate root cause analysis techniques (e.g. Pride problem solving)

  • Providing support ensuring external audit readiness and during external audits

  • Providing quality assurance guidance in support of process or product investigations

  • Facilitating product and process Corrective and Preventive Action (CAPA) investigations from issue identification through implementation of solution and effectiveness monitoring

  • Quality Management System activities such as: engineering change notice review and approval; procedure writing; nonconforming review and approval; delivery hold management, oversight and management of the CAPA system and quality planning

  • Leading Quality & Research projects ensuring timely completion of project deliverables, correcting issues delaying completion and reporting on status of projects

  • Leading and supporting continuous improvement initiatives

You are a part of our inclusive and innovative technical team of Engineers and Quality Assurance professionals at the Philips, Chichester site. Reporting to the Head of Service QA, this is a fantastic opportunity to work in a truly global role and develop skills and relationships across internal networks.

To succeed in this role, you should have the following skills and experience

  • Electrical, Mechanical Engineering or science discipline degree or a unique combination of education and experience may be substituted if they provide the essential skill sets for the position.

  • Experience in medical device industry preferred, with demonstrated understanding of and ability to interpret regulations and guidelines governing medical devices, including CFRs, ISO 13485, MDSAP, EU MDR.

  • Ability to manage and coordinate investigations and continuous improvement projects

  • Excellent technical writing, communication and organisational skills

  • Experience with MS Office products

  • Excellent oral and written communication and interpersonal skills

  • Ability to work independently and complete multiple assignments on time

In return, we offer you an innovative and challenging environment where you have the opportunity to use exciting system engineering skills to make a real difference to improving the lives of end-users of our products. As the business continues to grow and develop, there will be opportunities to progress within the organisation, travel to other sites and potentially relocate for Global opportunities.

Why should you join Philips?

Working at Philips is more than a job. It’s a calling to create a healthier society through meaningful work, focused on improving 3 billion lives a year by delivering innovative solutions across the health continuum at . Our people experience a variety of unexpected moments when their lives and careers come together in meaningful ways.

To find out more about what it’s like working for Philips at a personal level, visit the Working at Philips page at on our career website, where you can read stories from our employee blog at . Once there, you can also learn about our recruitment process at , or find answers to some of the frequently asked questions at .

Philips are an equal opportunities employer and welcome applications from all suitably qualified persons regardless of their race, sex, disability, religion/belief, sexual orientation or age.