Innovation Excellence Quality Engineer
Listed on 2026-05-07
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Engineering
Quality Engineering, Biomedical Engineer -
Quality Assurance - QA/QC
Quality Engineering
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function: Quality
Job Sub Function: R&D/Scientific Quality
Job Category: Professional
All Job Posting Locations: Danvers, Massachusetts, United States of America
Job Description: We are searching for the best talent for an Innovation Excellence Quality Engineer to be based in Danvers, MA.
About Med Tech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at
Purpose: This person will have the opportunity to perform various Design Quality Engineering functions supporting continuous improvement and innovation of marketed products! Activities will include risk management, design verification, design validation, design assurance activities, as well as manufacturing process development support, statistical analysis and more! This role’s emphasis will be in support of Abiomed’s existing single‑use heart pumps.
You will be responsible for:- Support Design Assurance engineering activities in support of Abiomed’s Life Cycle processes including design controls, quality planning, risk assessments/analysis/management, design reviews, test method development and validation, design and process verification and validation test plans and reports, post‑market monitoring, investigations, follow‑up and reporting.
- Navigate existing FMEAs and Hazard Analysis in support of sustaining and lifecycle activities.
- Ensure that FDA and other regulatory knowledge and experience is applied to risk and testing assessments.
- Work with manufacturing engineering to ensure necessary process controls are in place for design changes.
- Review and approve Engineering Change Requests (CR’s) and support the Non‑Conformance (NC’s) process as necessary.
- Act as an effective team member in the execution of Quality functions in compliance with FDA QMSRs (Design Control, CAPA, etc.), ISO 13485, MDD, CMDR, CMDCAS and other national and international quality and regulatory requirements and standards.
- Contribute to the design, development and implementation of product assurance plans providing feedback to corrective and preventative actions to engineering, manufacturing, service and field operations and supplier performance.
- Collect, analyze & report on quality system metrics: CAPA, complaint trends, manufacturing trends, etc.
- Develop statistically sound sampling plans and perform data analysis.
- Be a voice of quality and ensure compliance to internal & external quality standards.
- Bring ideas that challenge current thinking.
- Bachelor degree in Engineering or Sciences is required;
Masters desired. - 0 – 2 years of quality experience.
- Experience in the medical device industry as well as cardiovascular devices highly preferred.
- Demonstrates knowledge of quality engineering policies, principles and best practices and FDA/ISO requirements.
- Takes initiative and works well in a team environment.
Required Skills: Agility Jumps, Business Behavior, Compliance Management, Continuous Improvement, Database Backup, Data Gathering and Analysis, Data Savvy, Disruptive Innovations, Execution Focus, Issue Escalation, Process Oriented, Product Improvements, Quality Control (QC), Quality Control Testing, Quality Management Systems (QMS), Quality Standards, Regulatory…
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