Engineer II, Product Sustaining - Wayne, NJ

Getinge; Wayne (NJ); Hybrid; USD 100,000 - 105,000; Full time

Benefits offered by this job

Health Insurance

401k Plan with company match

Paid Time Off

Wellness initiative & Health Resources

Life Insurance

Short and Long Term Disability

Flexible Spending Accounts

Parental and Caregiver Leave

Tuition Reimbursement

Job summary

Getinge is seeking a Product Sustaining Engineer II in Wayne, NJ, to support sustaining activities for released medical devices, including design changes and CAPA, while ensuring regulatory compliance and supply continuity.

You will analyze complaints, perform engineering changes, and prepare technical documentation in a collaborative, cross-functional environment with a focus on quality and cost reduction. A B.S. in Mechanical Engineering and 3+ years in a regulated field are required.

Qualifications

• B.S. in Mechanical Engineering; advanced degree considered in lieu of experience
• 3+ years in progressive engineering roles, preferably in medical device or regulated industry
• Knowledge of FDA regulations, ISO 13485, and GMPs
• Experience with CAD and engineering drawings; GD&T and tolerance analyses
• Familiarity with design changes and CAPA processes
• Strong analytical and communication skills
• Ability to work cross-functionally and manage multiple priorities

Responsibilities

• Sustain engineering activities for released medical devices.
• Investigate complaints, nonconformances, field issues, and failures.
• Design and implement engineering changes through change control processes.
• Prepare drawings, specs, test protocols, reports and justifications.
• Perform tolerance, stress, material, and failure analyses.
• Conduct design verification/validation testing for changes.
• Support cost reduction, obsolescence, supplier and material changes.
• Participate in root cause investigations and CAPA implementations.
• Ensure compliance with FDA QSR, ISO 13485 and international standards.
• Provide technical support to QA, Operations, Regulatory and Customer Support.

Skills

Mechanical engineering principles

GD&T

Design for injection molded components

CAD software (SolidWorks/Creo)

Design control

Root cause analysis

FDA/ISO regulations

Analytical problem-solving

cross-functional teamwork

multitasking and prioritization

Education

Bachelor of Science in Mechanical Engineering

Tools

SolidWorks

Creo

Job description

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Date: Oct 20, 2026

Location: Wayne, NJ, US

Company: Datascope Corp.

Remote Work: 1-2 days at home (site based)

Salary Range: Salary range: $100k - $105k, 8% STIP

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 Product Sustaining Engineer II is responsible for sustaining engineering activities including product improvements, design changes, cost reduction initiatives, component obsolescence management, manufacturing support, complaint investigations, and corrective and preventive actions (CAPA). This position works under general supervision and collaborates with cross-functional teams to ensure product quality, regulatory compliance, reliability, and continuity of supply.

Job Responsibilities and Essential Duties

• Support sustaining engineering activities for released medical device products.
• Investigate product complaints, manufacturing nonconformances, field issues, and returned product failures.
• Design and implement engineering changes through established change control processes.
• Prepare and maintain engineering documentation including drawings, specifications, test protocols, reports, and technical justifications.
• Perform engineering analyses including tolerance stack-up analyses, stress calculations, material selection, and failure analysis.
• Conduct design verification and validation testing to support product changes.
• Support cost reduction projects, component and material changes, supplier changes, and product obsolescence issues.
• Participate in root cause investigations and implementation of corrective and preventive actions (CAPA).
• Ensure compliance with FDA Quality System Regulations, ISO 13485 requirements, and applicable international regulatory standards.
• Provide technical support to Quality, Operations, Service, Regulatory Affairs, and Customer Support organizations.
• Bachelor of Science degree (or equivalent), preferably in Mechanical Engineering.
• Minimum 3+ years of progressive and relevant engineering experience, preferably in the medical device or other regulated industry. Advanced degree considered in leu of experience.
• General understanding of Good Manufacturing Practices, FDA regulations, and ISO requirements.

Required Knowledge, Skills and Abilities

• Understanding of mechanical engineering principles, materials, manufacturing processes, and product development methodologies.
• Knowledge of engineering drawings, GD&T, tolerance analysis, and material properties.
• Understanding design of injection molded plastic, casting, sheet metal, machined components, and pneumatics preferred.
• Experience using CAD software such as SolidWorks, Creo, or equivalent preferred.
• Understanding of Design Control processes and engineering change management.
• Working knowledge of root cause analysis methodologies and problem-solving tools.
• Basic understanding of FDA regulations, ISO 13485, and other applicable medical device regulations preferred.
• Strong analytical and problem-solving skills.
• Self-motivated with the ability to accomplish project goals with minimal supervision.
• Effective verbal and written communication skills.
• Proficiency in Microsoft Office applications including Excel, Word, and PowerPoint.
• Ability to work effectively within cross-functional teams.
• Ability to manage multiple priorities while meeting project deadlines.

Salary range: $100k - $105k, 8% STIP

#LI-LG1 #LI-Hybrid

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
• 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.