Quality Engineer II at Medtronic-Switzerland

Geleen, Limburg, Netherlands -

Full Time

Start Date

Immediate

Expiry Date

10 Jun, 26

Salary

82800.0

Posted On

12 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality System Support, Regulatory Requirements, QMS Processes, Audits, Certifications, Nonconform Product Investigations, Root Cause Analysis, Corrective Actions, Preventive Actions, Trend Analyses, Compliance, FDA Regulations, ISO Requirements, Data Analysis, Problem-Solving, Communication

Industry

Medical Equipment Manufacturing

Description

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Bring your talents to an industry leader in medical technology and healthcare solutions – we’re a market leader and growing every day. You can be proud to part of technologies that are rooted in our long history of mission-driven innovation. You will be empowered to shape your own career. We support your growth with the training, mentorship, and guidance you need to own your future success. Together, we can transform healthcare. Join us for a career in IT that changes lives. Responsibilities may include the following and other duties may be assigned: Provides Quality System support and guidance to maintain compliance with all FDA and international regulatory requirements Supporting the Articulating Technologies QMS. Working as a pragmatic partner with the organization to ensure QMS processes related to General QMS & Pilot production are established, implemented and maintained in a compliant manner Supporting the EU OU Surgical entities from a Quality Oversight perspective consisting of pro-active support (example helping, supporting entities with setting-up QMS processes, audits & certifications) & re-active support related to production quality issue resolution, PHO and FCA support) Coordination and/or preparation of internal and external audits in accordance with regulatory standards (includes FDA and its equivalents outside the US as well as other government regulatory agencies / authorities) for the Operating Unit Owns and drives Nonconform product Investigations, Root Cause Analysis and resultant Corrective Actions and Preventive Actions, performs trend analyses and report compliance observations to identify areas in need of improvement and investigates and resolves compliance problems, questions, or complaints received from other units of the company, customers, government regulatory agencies, etc. Masters knowledge of applicable Quality, FDA (Food & Drug Administration) Medical Device Directives/ Regulation, and ISO (International Organization for Standardization) requirements through the updating of policies and procedures and acting as a liaison with appropriate policy experts Excellent writing and editing skills, and computer skills and able to travel within EU and International approximately 10-25%. Required Knowledge and Experience: Relevant bachelor’s degree with a minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience Demonstrated knowledge of all quality system elements and regulatory requirements (i.e. FDA, GMP, QSR and ISO 13485, and MDSAP) for finished medical devices with the ability to effectively implement and communicate those requirements in a government regulated healthcare industry and knowledge of Medical Device Manufacturing processes/requirements Effective usage of data analysis tools, analytical and research skills, and problem-solving techniques with keen attention to detail and simultaneous understanding of the "big picture" and desire to follow an audit trail to identify risks, non-conformances, true root cause, etc. Outstanding written, oral communication, and presentation skills Sound judgement, ability to make decisions, work independently and ability to manage and execute on multiple critical projects simultaneously. Capable to manage multiple priorities and escalate issues. 2 or more years relevant experience in a Medical Device Manufacturing setting or equivalent like packaging and labeling and/or distribution and experience supporting and or participating in regulatory inspections and audits are considered advantages for this role. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Netherlands: 55,200.00 EUR - 82,800.00 EUR | This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). About Medtronic We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity here We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. We change lives. Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That’s who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives. We build extraordinary solutions as one team. With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough. This life-changing career is yours to engineer. By bringing your ambitious ideas, unique perspective and contributions, you will… Build a better future, amplifying your impact on the causes that matter to you and the world Grow a career reflective of your passion and abilities Connect to a dynamic and inclusive culture that welcomes the challenge of life-long learning These commitments set our team apart from the rest: Experiences that put people first. Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need. Life-transforming technologies. No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms. Better outcomes for our world. Here, it’s about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls. Insight-driven care. Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities. For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support. This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here. For updates on job applications, please go to the candidate login page and sign in to check your application status. If you need assistance completing your application please email AskHR@medtronic.com To request removal of your personal information from our systems please email RS.HRCompliance@medtronic.com

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

This role involves providing Quality System support to maintain compliance with FDA and international regulatory requirements, specifically supporting the Articulating Technologies QMS and EU OU Surgical entities with proactive and reactive quality oversight. Responsibilities also include coordinating and preparing for internal and external audits, owning nonconform product investigations, driving root cause analysis, and reporting compliance observations.