• Responsible for ensuring that ShipERP products are functioning as designed and minimizing product defects by identifying bugs and missing functionalities based on given product requirements. • Create test cases and test data for various test scenarios • Execute and document test scripts and analyze results • Review of test scripts • Identify and isolate bugs in software • Basic troubleshooting of product issues/bugs • Identify potential issues in user interface • Identify other areas of improvement for the product • Understand the functionality and business process related to the product • Coordinate with Business Analysts and Developers regarding the expected functionality of the product to verify test execution and results

About ScienceLogic… ScienceLogic is redefining IT operations for the modern enterprise. Our AIOps platform empowers organizations to achieve Autonomic IT — where systems are self-healing, self-optimizing, and seamlessly aligned with business outcomes. We help enterprises and service providers gain unified visibility across hybrid and multi-cloud environments, automate workflows, and unlock performance at scale. We’re accelerating digital transformation through the power of automation, AI, and analytics — giving IT and business leaders the tools to deliver superior customer experiences, drive efficiency, and innovate with confidence. QA Systems Engineer What we are looking for… We are looking for a QA Systems Engineer to own and evolve a critical engineering lab environment that supports product development, testing, and validation. This role combines infrastructure ownership with hands-on QA engineering, acting as “Customer Zero” to ensure product quality in real-world scenarios before release. You’ll work across cloud and on-prem environments, collaborate with multiple engineering teams, and play a key role in ensuring scalability, reliability, and performance. What you’ll be doing…. • Coordinate testing activities across shared lab resources and multiple engineering teams • Manage, maintain, and optimize lab infrastructure used for development and testing • Deploy and upgrade applications across lab environments and cloud platforms (AWS, Azure, GCP) • Develop and maintain simulators and mock devices to support internal testing needs • Partner with QA leads to review and approve test plans and UAT standards • Design and execute backend, end-to-end, security, and performance tests • Generate and present reports (defect, execution, summary) for Product and Engineering stakeholders • Identify, provision, and scale resources to ensure lab reliability and performance • Conduct scale testing and capacity planning analysis Qualities you possess…. Must Haves • Bachelor’s degree in a related field or equivalent experience • 3–7 years of experience in infrastructure, cloud management, software testing, or QA engineering • Strong experience with both manual and automated testing methodologies • Proven ability to design and execute backend, end-to-end, security, and performance tests • Solid troubleshooting and analytical problem-solving skills • Experience creating test plans, strategies, scopes, and automation frameworks • Deep understanding of QA methodologies (black box, white box, gray box, test design, execution) • Strong understanding of SDLC best practices • Experience writing SQL queries for backend validation (MySQL, Oracle) • Knowledge of enterprise networking concepts (SNMP, MIBs, clustering) • Proficiency in scripting/programming (e.g., Python, JavaScript, PowerShell, Ansible, REST APIs) • Experience leveraging AI-assisted development and testing tools (e.g., Codex, Tabnine, Claude) to improve test design, automation, and troubleshooting efficiency • Excellent written and verbal communication skills with strong attention to detail Nice to Have • Experience testing across Linux, Windows, and macOS environments • Experience working in Agile development environments • Familiarity with automation frameworks (e.g., Selenium, TestCafe, BDD) • Ability to present findings to both technical and non-technical stakeholders • Experience with hardware or software-defined simulation tools • Strong project planning and resource coordination skills Benefits & Perks - Comprehensive medical, dental and vision plans. - 401(k) plan with employer match. - Flexible Paid Time Off (FTO) so that you can take the time that you need to re-energize. - Volunteer Time Off (VTO) - take two days off per calendar year to volunteer with your preferred charitable organization. - 5-year Service Milestone Sabbatical. - Paid parental leave. - Generous employee referral bonus program. - Pet insurance. - HQ Office centrally located in Reston Town Center featuring a well-stocked kitchen with rotating snacks and beverages, and catered lunch on Thursdays. - Regular virtual company-wide events, including cooking classes, yoga, meditation and more. - The opportunity to learn and develop from some of the best and brightest minds in the industry! Don’t meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At ScienceLogic, we are dedicated to building a diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or any other applicable legally protected characteristics in the location in which you are applying. About ScienceLogic ScienceLogic is a leader in IT Operations Management, providing modern IT operations with actionable insights to resolve and predict problems faster in a digital, ephemeral world. Its solution sees everything across cloud and distributed architectures, contextualizes data through relationship mapping, and acts on this insight through integration and automation. www.sciencelogic.com

Title: Quality Sustaining Engineer Location: Fraser United States Job Description: 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 Quality Sustaining Engineer, you will play a key role in ensuring that Healthmark product across Getinge's Infection Control Consumables portfolio meet applicable quality requirements. This includes FDA Class I and II medical devices, EU MDR Class I devices, and selected non-regulated products. You will work cross-functionally with Regulatory Affairs, R&D, Manufacturing, and Operations to support compliant product lifecycle management on Healthmark products for design transfer deliverables and resulting acceptance activities and production and process controls for both Healthmark designed and distributed products. Job Responsibilities and Essential Duties: - Support design change transfer deliverables and activities in accordance with FDA Quality System requirements (21 CFR Part 820 / QMSR) requirements for Class I, II devices, EU MDR (2017/745) requirements for Class I devices, and applicable internal quality system procedures. - Ensures critical-to-quality (CTQ) attributes from product designs are reflected in product and materials acceptance activities, equipment qualification, calibration, PM requirements, validations, and facility production and process controls. - Provide quality engineering input in the design, fabrication, development, installation, validation, and qualification of equipment / processes which may include feasibility studies and/or proper documentation for justification of project and training. - Lead cause-identification and problem-resolution for various types of quality, production or service-related issues. Including product complaints, nonconformance report evaluations of factory issues as well as evaluations of factory caused Out of Box failures. - Serve as a Quality subject-matter expert for PFMEA and production related risk management files per ISO 14971: 2019. - Participate in production process work instruction development and review of changes. - Support internal and external audits by providing clear rationale and objective evidence for role area of responsibilities. - Ensures comprehensive measurement systems and trending is in place to monitor effectiveness of quality and reliability systems to identify, bracket, correct and prevent defects. Required Knowledge, Skills and Abilities: - Demonstrated leadership, problem-solving, decision-making, influencing, facilitation, and communication skills, with the ability to engage effectively at all organizational levels. - Must have the ability to assess the impact of quality management strategies on business performance. - Must have in-depth knowledge of all applicable Quality and Regulatory standards 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. Monday-Friday, 8:30am-5:00pm $75,280-$94,100 + 4% STIP #LI-LG1 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.

Role Description The Senior Automation Solutions Consultant is responsible for prospecting, scoping and closing Laboratory Automation Solutions in the Pharma, Synthetic Biology and Clinical spaces. This position reports to the Regional Sales Manager and is part of the Life Science Automation Team located in Sacramento or San Francisco Bay Area and will be working remotely to cover Berkeley, San Francisco Bay, Oregon and Sacramento. Candidate will ideally live in Sacramento or San Francisco Bay Area. In this role, you will have the opportunity to: - Work with your Field Application Specialist and Field Project Manager to scope and deliver Laboratory Automation Solutions. - Understand and grow market share in your territory. - Represent the organization in customer negotiations, trade shows, seminars, conferences and other official occasions. - Collaborate with other team members to provide best in class automated solutions. - Deliver Territory Sales Quota for Hardware and Consumables and participate in continuous improvement processes to benefit the whole team. - Champion Danaher core values and the use of DBS, ensuring team members are actively engaged in the achievement of the company growth objectives. - Continuously drive Voice of the Customer (VOC) back into all parts of the business to ensure customer’s interests are prominently positioned. - Advocate for the customer, for product quality and for providing excellent customer solutions, consistently striving to increase customer satisfaction. Qualifications - BA or BS in Science, Chemistry, Biology or Environmental Science or equivalent. - 3+ years of experience in sales (direct and engaging distribution channel partners preferable) in North America with deep knowledge and understanding of the North America Biopharma, Academia, Government and Life Sciences markets. - Previous exposure to Laboratory Automation is highly desirable. - Clinical, Pharmaceutical, or Synthetic Biology Lab Experience. - Strong analytical skills, problem-solving attitude and solid business acumen. - Ability to work in a demanding, fast-paced and action-oriented environment. Requirements - Ability to travel – 25% travel, overnight within your territory or other locations. - Must have valid driver’s license with an acceptable driving record. Benefits - Comprehensive package of benefits including paid time off. - Medical/dental/vision insurance. - 401(k) to eligible employees. - Remote work arrangement eligible for this position. - Annual salary range of $115,000-$140,000. - Eligible for bonus/incentive pay.