Quality Engineer, Product Safety

Quality Engineer, Product Safety page is loaded

Quality Engineer, Product Safety

Apply locations Farnborough time type Full time posted on Posted Yesterday job requisition id 561783

Job Title

Quality Engineer, Product Safety

Job Description

In late January, we announcedthat Bridgefield Capital signed an agreement to acquire Philips’ Emergency Care business which includes leading brands and products like HeartStart AEDs, Intrepid and DFM100 monitor defibrillators, Tempus monitor and Tempus ALS systems, and Corsium and ECI informatics solutions. We expect the transaction to close at the end of 2025.

With Bridgefield’s support and building on our 40+ year legacy of growth and innovation in emergency medical technology, the Emergency Care business will continue passionately pursuing our mission of saving lives, lowering the cost of healthcare, and advancing the science of resuscitation while serving the public access AED, EMS, military, and hospital market segments.

In this role and as part of an agile company that has the dedicated resources needed to achieve its strategic goals, you’ll have every opportunity to become a part of the “NewCo” we are forming and grow both personally and professionally and potentially make an even bigger impact on the acute care space – as well as on the consumers, patients and healthcare workers who depend on these innovative life-saving solutions.

Quality Engineer – Product Safety

Help to ensure the product safety of our Emergency Care medical devices and join is in our mission is to empower and enable our customers – from clinicians to paramedics, first responders to the everyman – to save lives using our innovative, market-leading technology.

Your role:

• Join our team as a Quality Engineer to play a key role in our Product Safety, property and environmental risk management, contributing to the safety & efficacy of medical products that save lives and improve health.

• You will collate post market information, analyse, and then facilitate the decisions needed to manage risk and ensure product safety, including the management of Issue Impact Assessments and Risk Files.

• Working in partnership with Complaints, Post Market Surveillance, R&D, Clinical, Regulatory and Corrections & Removals.

• Be sure to ask your recruiter to share information on the compensation package

How we work together

• We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.

• This role is based from our Farnborough, Hampshire office.

You’re right for this role if:

• You have experience in the Risk Management Process in a regulated environment and have worked hands-on with ISO 14971 standard.

• You have a good understanding of risk management requirements, tools, methodologies, and processes, including use of a variety of accepted methods.

• You describe yourself as organised and methodical, comfortable with working in the detail of a Quality Management Systems and regulatory requirements.

• You are comfortable analysing post market data to detect patterns, support decisions and produce reports for leadership teams.

• You bring with excellent teamwork skills able to influence and build rapport with internal customers and stakeholders.

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 .

#LI-EU

#LI-hybrid

Similar Jobs (1)

Senior Supplier Quality Engineer

locations Farnborough time type Full time posted on Posted 5 Days Ago

At Philips, we believe that every human matters. As a global health-tech leader, we focus on improving people’s health and wellbeing through meaningful innovation. The people who work here share our passion and are motivated to bring this purpose to life.

For more than 130 years, we have been creating technologies and innovations that improve people\’s lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health.

Together, we deliver better care for more people because we believe that every human matters. That\’s why we\’re taking steps to create an environment where we acknowledge and embrace our differences and uniqueness and listen to and value each other\’s views. When people feel cared for and listened to, they bring their best qualities to work, leading to better collaboration, communication, innovation and success.

It is the policy of Philips to provide equal employment and advancement opportunities to all qualified employees and applicants for employment without regard to race, color, religion, sex, pregnancy/childbirth or related medical conditions, age, ethnic or national origin, sexual orientation, gender identity or expression, physical or mental disability, genetic information, citizenship status, veteran or military status, marital or domestic partner status or any other characteristic protected by law. As an equal opportunity employer, Philips is committed to fostering a culture where all are treated with respect and professionalism.

To ensure reasonable accommodations for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans\’ Readjustment Act of 1974 and Title I of the Americans with Disabilities Act of 1990, applicants that require accommodation in the job application process may contact 888-367-7223, option 5, for assistance.

Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace.

#J-18808-Ljbffr