Sr. Quality Sustaining Engineer

With a passion for life Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers. Are you looking for an inspiring career? You just found it. Job Overview As a Senior Quality Sustaining Engineer, you will play a key role in ensuring that Healthmark products across Getinge’s Infection Control Consumables portfolio meet applicable quality and regulatory requirements. This includes FDA Class I and II medical devices, EU MDR Class I devices, and selected non-regulated products. In this role, you will take ownership of quality engineering activities within the product lifecycle, including design changes, production quality, and post-market support. You will work cross-functionally with Regulatory Affairs, R&D, Manufacturing, and Operations to drive compliant and effective product lifecycle management while independently leading initiatives and contributing to continuous improvement efforts. Job Responsibilities and Essential Duties: Lead design change transfer deliverables and activities in accordance with FDA Quality System requirements (21 CFR Part 820 / QMSR), EU MDR (2017/745), and applicable internal quality system procedures Take ownership of quality engineering deliverables for assigned products or projects, ensuring compliance with regulatory requirements and internal procedures throughout the product lifecycle Ensure critical-to-quality (CTQ) attributes are appropriately defined and implemented, and support the development of acceptance activities, equipment qualification, calibration, validation, and production/process controls Provide quality engineering leadership and technical input in the design, fabrication, development, installation, validation, and qualification of equipment and processes, including feasibility assessments and documentation Lead root cause investigations and resolution of complex quality issues, including product complaints, nonconformances, and production-related issues, ensuring timely and effective corrective actions Serve as a Quality subject-matter expert for PFMEA and risk management activities in accordance with ISO 14971:2019, supporting risk-based decision-making Support development, review, and improvement of production process documentation, including work instructions and change control activities Support internal and external audits by preparing documentation, providing objective evidence, and participating in audit discussions Analyze quality data and trends (e.g., SPC, complaints, nonconformances) to identify improvement opportunities and support data-driven decision-making Drive and participate in continuous improvement initiatives to enhance product quality, process efficiency, and compliance Act as a key quality representative on cross-functional teams, collaborating with stakeholders to resolve issues and ensure alignment Build effective working relationships across functions, leveraging expertise from colleagues to achieve project and quality objectives Provide guidance and mentorship to less experienced engineers as needed Required Knowledge, Skills and Abilities: Demonstrated leadership in problem-solving and driving quality-related initiatives within cross-functional teams Strong decision-making and analytical skills, with the ability to apply risk-based thinking Ability to assess the impact of quality decisions on product performance and compliance In-depth knowledge of applicable quality and regulatory standards Experience with data analysis, trending, and statistical tools Effective communication and interpersonal skills, with the ability to collaborate across organizational levels Ability to manage multiple priorities in a fast-paced environment Minimum Requirements: Bachelor’s degree in science, engineering, or other technical areas; or equivalent job experience required. Advanced degree preferred; 5+ years of relevant experience in the medical device industry; and have several years of experience in Quality Engineering, Product / Manufacturing Quality or a related role within the medical device industry. Applied knowledge of ISO 13485:2016, ISO 14971:2019, 21 CFR 820 QSMR, and EU Medical Device Regulation 2017/745 (MDR). Working knowledge of international standards and regulations applicable to medical devices and combination products. Familiarity with Geometric Dimensioning and Tolerancing (GD&T) standards and principles. Experience in Statistical Process Control’s (SPC), data analysis, and trending. Ability to apply practical and technical problem solving to quality system and product improvements. Excellent interpersonal skills, including ability to work effectively cross-culturally and cross-functionally. Proven ability to effectively lead cross-functional team meetings Capable of developing matrix relationships with key colleagues in other functional areas and divisions; Recognizes other colleagues' areas of expertise and utilizes them effectively to achieve team objectives. Champions high quality deliverables, innovation, and appropriate risk-based decision making. Ability to understand the sensitivities within the Getinge’s environment. Excellent project management and interpersonal skills. Adaptable to changes in work environment. Ability to work in a fast-paced environment. The position is hybrid, with 25% travel as needed. Quality Requirements: Build Quality into all aspects of their work by maintaining compliance to all quality requirements. Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function). Must have the education and experience to understand and comply with U.S. and Worldwide medical device regulations (As applicable to your job function). Attend all required Quality & Compliance training at the specified interval. Adopt the “Beyond Compliance Quality Culture” in the work environment; always meet and exceed requirements. Environmental/Safety/Physical Work Conditions: Ensures environmental consciousness and safe practices are exhibited in decisions Use of computer and telephone equipment and other related office accessories/devices to complete assignments May work extended hours during peak business cycles This position is hybrid with up to 3 days in office The physical demands described here are a representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

$96,000-$120,000 + 5% STIP

About us With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries. Benefits at Getinge: At Getinge, we offer a comprehensive benefits package, which includes: Health, Dental, and Vision insurance benefits 401k plan with company match Paid Time Off Wellness initiative & Health Assistance Resources Life Insurance Short and Long Term Disability Benefits Health and Dependent Care Flexible Spending Accounts Commuter Benefits Parental and Caregiver Leave Tuition Reimbursement Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.