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.
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Job OverviewThe Standards Engineer II supports execution of product standards and compliance activities for complex electro-mechanical and software-driven medical devices. This role provides intermediate-level engineering execution capacity for standards-related work under the guidance of CSA, senior engineers, standards authorities, and technical subject matter experts.
The Standards Engineer II uses approved AI tools to support first-line standards and compliance assessment, then applies independent engineering diligence to verify assumptions, identify gaps or inconsistencies, and prepare issues for review and decision-making. The role is expected to exercise developing engineering judgment, manage assigned compliance actions, and drive disciplined follow-through through the Standards Action Board, SAF process, and related compliance workflows. The Standards Engineer II is not expected to serve as the final technical authority for standards interpretation but is expected to recognize when deeper SME review is required and organize the evidence, rationale, and questions needed to support timely decisions.
Job Responsibilities and Essential Duties- Use approved AI tools to support initial standards and compliance screening, summarize information, identify potential gaps or questions, and organize preliminary observations; independently verify outputs before use and route conclusions through CSA, technical SMEs, and applicable processes.
- Prepare, route, track, and follow up on Standards Assessment Forms or related standards and compliance workflow records, ensuring inputs, rationale, evidence, SME feedback, and decisions are documented and advanced through the defined process.
- Manage assigned standards and compliance action items under guidance, including intake, clarification, ownership tracking, due dates, status updates, and escalation of barriers to closure.
- Review inputs from engineers, CSA, Regulatory, Quality, and other stakeholders for completeness, consistency, traceability, and first-level technical plausibility; identify gaps, unclear rationale, or areas requiring deeper SME interpretation.
- Support Standards Action Board activities by preparing agendas, facilitating routine portions of meetings, documenting decisions and action items, and tracking follow-up to closure.
- Coordinate with CSA, technical SMEs, Systems Engineering, Regulatory Affairs, Quality, and other stakeholders to obtain inputs, align on next steps, and maintain forward progress on assigned compliance activities.
- Maintain clear, organized records of compliance asks, technical rationale, decision history, action status, evidence, and next steps in a manner that is accessible, auditable, and easy for technical owners to use.
- Proactively follow up with action owners, identify overdue or blocked items, communicate status clearly, and help convert compliance priorities into practical execution plans with appropriate guidance.
Minimum Requirements- Bachelor's degree in Engineering or a closely related technical discipline required or strongly preferred, consistent with an Engineer II role.
- Typically 2-5 years of relevant experience in engineering, medical devices, regulated product development, quality, regulatory, product compliance, or technical project execution.
- Ability to use approved AI tools responsibly to support first-line assessment, while applying independent diligence, verifying outputs, protecting confidential information, and confirming conclusions through appropriate technical review.
- Ability to understand technical inputs at an intermediate level, ask clarifying questions, identify inconsistencies, and engage engineers or SMEs when deeper technical judgment is required.
- Ability to manage action items, meeting outputs, follow-ups, documentation, and cross-functional inputs with strong attention to detail.
- Working familiarity with standards, compliance, design control, quality systems, or regulated product documentation preferred; deep standards subject-matter expertise is not required.
Required Knowledge, Skills, and Abilities- Developing engineering judgment sufficient to understand technical discussions, recognize incomplete or unsupported conclusions, and constructively challenge inputs at an intermediate review stage.
- Ability to use AI-enabled tools as an aid to organize information, develop preliminary observations, and identify questions for review, while recognizing that AI output is not a substitute for engineering diligence, objective evidence, or SME approval.
- Demonstrates a learning mindset, curiosity, and willingness to ask questions, seek feedback, and apply coaching from senior engineers, CSA, technical SMEs, and cross-functional partners.
- Uses clear communication to share observations, document decisions and objective evidence, raise concerns, and align with team members on assigned work.
- Works collaboratively in a team environment, demonstrating reliability, accountability for assigned tasks, and openness to different technical perspectives.
- Maintains attention to detail and follow-through when collecting inputs, documenting rationale, tracking action items, SAF status, SME feedback, and escalating issues appropriately.
- Ability to support cross-functional meetings, document outcomes, summarize status, and drive timely follow-up with action owners.
- Basic practical understanding of regulated documentation, design control concepts, quality systems, or standards-related workflows.
- Ability to work with technical SMEs to clarify inputs, surface gaps, distinguish execution issues from technical interpretation issues, and translate compliance direction into actionable tactical plans under appropriate guidance.
This is a "Defined Term" assignment that will last approximately 12 months or until project is complete. Defined Term employees are eligible for most benefits (including health insurance and paid time off) while on assignment.
Salary range: $100 - $105k
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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
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.
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