Job Title Quality Compliance Specialist Job Description Quality Compliance Specialist Support business and site level aspects of the quality management system for the Philips Image Guided Therapy Devices business. You will support sites within this business in continuous maintenance and improvement of the Quality Management System and its subsystems. You are responsible for Assisting Quality Manager (as auditee) for Audits (internal & external) Quality CAPA Owner/Approver for all CAPAs Quality Facilitator/Approver for all NCRs Assisting the EC MDD Authorized Rep with mandatory vigilance reporting & FSCAs to Notified Bodies, Competent Authorities and Customers within the EU Implementing and maintaining the Quality Management System according to the European and International regulations/guidelines; ISO 13485:2016, FDA 21CFR 820, EUMDR 2017/745 Updating (incl. writing of) of SOPs/WIs to ensure the highest compliance to our standards Quality approver of QMS changes in lieu of the Quality Manager Maintaining (in view of audit readiness) all QMS documents (& records) in relation to operational & commercial processes (incl. field sales, Customer Service and Order Management etc.) Ensuring that the Complaint Device Handling is done in a timely and orderly manner Updating/maintaining the Complaint handling database/SAP searches to aid complaint investigations Supporting the Quality and Operations Team with the implementation of processes – incl. System Installations Supporting the Operations Team with the physical distribution of our products (incl. logistics) Maintaining LMS Training tool for International (incl. aiding people managers in annual reviews etc.) Assisting the Quality Manager and Team with the onboarding processes of new hires Support and sometimes execute change notices within the Document Controls system (Windchill) ensuring appropriateness and effectiveness. Escalate areas of non-compliance, risk and/or potential improvement to Management and develop plans for appropriate action to address causes of deficiencies. Identify and investigate potential trends for improvement initiatives. Maintaining the highest level of compliance (in the form of training sessions) for the employees You are a part of The international Quality team for our Image Guided Therapy Devices department and support any IGTD site as needed. We are a very diverse and dynamic team, located in Best (NL) and USA. To succeed in this role, you’ll need a customer-first attitude and the following Bachelor's / Master's Degree in Mechanical Engineering, Industrial Engineering, Science or equivalent. You’ve acquired 5+ years of experience in Quality Management Systems, Regulatory Compliance, Auditing with medical device or a regulated industry, preferred. Your skills include proficiency in of ISO 9001, ISO 13485, FDA CRF 21 part 820 and Good Manufacturing Practices (GMP). Fluent in English, any other language is an advantage 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. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. This is an office role. Compensation & benefits for Best location (NL) Doing meaningful work should come with fair, transparent rewards. The base salary range for this role is €61,185.00 –€101,975.82. We determine pay within the range using objective factors, like the skills the role requires, your relevant experience and the responsibility you'll have in this role, alongside internal equity and local market considerations. This role is eligible for 3% bonus with your rewards linked to your KPIs and company results. We’ll share the full approach with you during the interview process, so you can make a clear, informed decision. About Philips Are you ready to do the work of your life to help the lives of others? Learn more about our business, discover our rich and exciting history and 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 culture of impact with care. #LI-EU 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. We’re committed to building a diverse and inclusive workplace culture where people feel heard, valued and connected. Because we know the possibilities are unlimited when people feel empowered to grow and succeed together. It is the policy of Philips to provide equal employment and advancement opportunities to all colleagues and applicants for employment without regard to age, color, citizenship, disability or perceived disability, ethnicity, gender, gender identity or expression, genetic information, marital or domestic partner status, military or veteran status, national origin, pregnancy/childbirth, race, religion, sexual orientation, or any other category protected by federal, state and/or local laws. For US applicants only: Philips is an equal employment opportunity and affirmative action employer Disability/Veteran. Click here to review "EEO Is The Law and Supplement” Poster. Click here to review the Pay Transparency Nondiscrimination Statement. As an equal opportunity employer, Philips is committed to a diverse workforce. In order to ensure reasonable accommodation 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.

Quality Compliance Specialist.

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