Sr. Engineer, Compliance - Wayne, NJ

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

The Senior Compliance Engineer is responsible for ensuring that Cardiac Assist electromechanical medical devices meet all applicable global regulatory, quality, and safety requirements throughout their lifecycle. This role provides technical leadership across product safety, electrical safety, design control compliance, labeling and safety markings, environmental/material compliance (RoHS/REACH), and global market‑access requirements, ensuring products remain aligned with state‑of‑the‑art expectations.

The Senior Compliance Engineer serves as a critical interface between Engineering, Quality, Regulatory Affairs, Supplier Quality, and Manufacturing, ensuring that product designs, sustaining engineering activities, and change initiatives remain audit‑defensible, traceable, risk‑based, and compliant across international markets.

Job Responsibilities and Essential Duties

• Lead compliance evaluations for new designs, design changes, sustaining engineering, and remediation activities.
• Interpret and apply global standards including IEC 60601‑1 series (electrical safety), IEC 60601‑1‑8, IEC 60601‑1‑12, EN 1789, GB 9706 series, UL/CSA, and other applicable international product and safety requirements.
• Support development and verification of labeling, product safety markings, regional electrical requirements, and market‑specific compliance deliverables (EU MDR, FDA, China, LATAM).
• Conduct compliance impact assessments during design reviews, ensuring requirements, risks, verifications, and mitigations are aligned with global expectations.
• Ensure compliance documentation is complete, consistent, and audit‑ready (DHF/Technical File), including traceability, risk management, verification and validation records, and certification artifacts.
• Provide guidance on environmental and material compliance (RoHS, REACH, China RoHS) and ensure supplier documentation meets regulatory expectations.
• Support CAPA investigations that require compliance input, including evidence review, standards interpretation, and risk‑based justification.
• Maintain awareness of emerging regulatory changes and state‑of‑the‑art updates; drive integration into engineering processes and technical documentation, and identifying required retesting with recognized third party test labs.
• Support global regulatory submissions (510(k), EU MDR Technical Documentation, and regional registrations) with compliance rationale and evidence.
• Collaborate with Supplier Quality and Procurement to evaluate compliance of purchased components, including safety‑critical and regulated materials.
• Support internal and external audits, inspections, and technical inquiries, ensuring timely, accurate, and well‑documented responses.
• Guide engineering teams in applying compliance principles early in product development to reduce downstream redesign and accelerate global approvals.

Minimum Requirements

• BS in Systems, Biomedical, Electrical, or Software Engineering with 8+ years of related experience
• MS or PhD in Systems, Biomedical, Electrical, or Software Engineering with 6+ years of related experience
• Demonstrated experience working with relevant medical device regulatory and product‑safety standards (e.g., IEC 60601‑1, ISO 14971, IEC/ISO environmental testing, labeling requirements, or international certification processes).

Required Knowledge, Skills, and Abilities

• Proven experience supporting compliance evaluation, maintenance, or certification of electromechanical medical devices.
• Strong understanding of medical electrical safety (IEC 60601‑1 series), product safety principles, risk management (ISO 14971), and global market‑access requirements.
• Working knowledge of FDA QMSR, ISO 13485, ISO 14971, EU MDR and related regulatory frameworks.
• Ability to interpret technical compliance reports (e.g., electrical safety, environmental compliance, risk controls, labeling/marking evaluations), identify gaps, and guide engineering teams toward compliant solutions.
• Strong analytical and problem‑solving skills with ability to apply risk‑based decision making.
• Excellent verbal and written communication skills, including preparation of audit‑ready technical documentation.
• Ability to work cross‑functionally and communicate effectively with engineers, quality, regulatory, suppliers, and certification bodies.
• Strong organizational skills with the ability to manage multiple priorities in a regulated environment.
• Ability to participate in and lead technical meetings, design reviews, and compliance‑focused assessments.

Salary range:  $120k – 135k

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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
• 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.