Job Title Quality Manufacturing Engineer (m/f/d) Job Description Your role: Accompanying as a Team Member for New Product Innovation (NPI) Projects for all design transfer activities and ensure that the design output meets the established manufacturing requirements according to DMR, product Quality and Quality regulation. Reviews and approves deliverables in accordance with requirements outlined in the Design Control, Production Process Controls process and other applicable ISO Standards and FDA Regulation e.g. ISO 13485, ISO14971, CFR21Part820, etc. Accompanying Process Changes to Products in the Factory line together with other relevant stakeholders for Products which are already distributed to the Market to ensure, all relevant quality policies, Procedures, and work instructions of the quality management system have been updated and trained before release of the Change according to the mentioned Standards appropriate risk mitigations within Risk management e.g. PFMEA were considered so that the overall risk level remains acceptable before release. Verify that production processes for the devices, including process validation (if required) have been defined, verified, documented, and implemented. Handling of Non-conforming Products/Part/Material characteristics for Production area together with MRB Lead, Supplier/Manufacturing Engineering as well as Incoming inspection Team. Support audits as back room lead or back room team member for internal and external audits Your the fit if: You have 3 years work experience as Engineer in a highly regulated industry (preference for the medical device industry) Strong technical understanding of manufacturing processes, preferred with regard to form-fit-function and material-bonding joining technologies Experience with shopfloor management tools to drive operational excellence and real-time quality monitoring You have experience with Process and/or Software Validation methodologies combined with Risk management knowledge (e.g. PFMEA) to validate key product designs on production process level and related IT-Interfaces You have understanding of handling non-conforming Products, CAPAs and Quality Plans Knowledge with application of Standards/Regulations like ISO13485, ISO14971, 21CFR820 You are a social team player who thrives in a global cross functional environment You have good communication skills verbal and in writing You have a hands-on and solution-oriented mentality with a high focus on Quality for product and production processes. You are business fluent in both English and German languages Philips benefits for you: Purpose: Doing meaningful work with a great team Hybrid work concept: Up to two days a week "working from home" Philips Pension Fund: Employer-funded pension plan Mobility and devices: public transport ticket, leasing bicycles, cars, and also smartphones for private use Culture: Informal culture, a paid day for voluntary work, various team/cultural activities (on sustainability, diversity, ), etc. Philips University: Wide range of professional training courses and for personal development Philips MyShop: Discount on Philips products Philips in Balance: Various offers for physical and mental health and sports courses “Partnerzeit” – two paid weeks off after your partner has given birth Meals: Free drinks and low prices in our canteen and Café Philistro 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. Discover our rich and exciting history. Learn more about our purpose. 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 .