Job Title Correction & Removal Manager Job Description In late January, we announced that 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. As a Corrections and Removal Manager, you will ensure an effective and adequate process for executing field actions / Corrections and Removals for the Emergency Care global business. Your role: Ensure that processes for specifying and executing field actions / corrections and removals are adequate and meet the expectations of all key stakeholders (customers and regulatory agencies). Be part of the Corrections and Removal Strategy and Planning team. A cross-functional team between regions quality, regions service, & legal manufacturers (business units), where you will provide feedback and regional input to ensure consistent decision making across Philips Businesses and Markets. Promptly identify potential reportable and safety related C&R, ensuring timely notification of regulators and affected customers. Facilitate the preparation of key field actions documents such as Field Safety Notices and Field Safety Corrective Actions. Submits FSCA package to the Competent Authorities and or other regulatory agency as required by Country/Market. Monitors KPI and escalates when needed to ensure timely closure. You will work together with global C&R Specialist, Service, R&D and Quality, ensuring that respective processes are timely, effective, and efficient. You're right for the role if you have: Bachelor of Science in engineering or science degree and a related experience in the medical device. Direct experience in Quality (such as CAPA, QMS, Complaints) with an interest in developing expertise in Corrections & Removals. Ideally a background with global medical device regulations, requirements, and standards such as ISO13485, ISO9001, MDD, European Medical Device Regulation (MDR), FDA QSR, but will also consider other regulated industries (aerospace, automotive, defence). An agile mindset, eager to embrace change and seek continuous improvement. A collaborative approach with experience working cross functionally. 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 will be based in our office in Farnborough, Hampshire. LI-EU LI-Hybrid