Michael Page
Design Quality Engineer - Medical Devices - Westborough, MA
Michael Page, Westborough, Massachusetts, United States, 01581
The Design Quality Engineer in Medical Device Manufacturing will lead quality system and design assurance activities for New Product Development (NPI), ensuring compliance with FDA 21 CFR Part 820, ISO 13485, and EU Medical Device Regulations. They will play a key role in maintaining quality standards for Class III medical devices throughout the product lifecycle at our Westborough, MA facility.
Client Details
My client is a leading innovator in the field of electrophysiology, specializing in advanced solutions for the treatment of atrial fibrillation (AFib). Their state-of-the-art technologies, including laser-based and pulsed-field ablation (PFA) systems, are designed to improve the precision, efficiency, and outcomes of cardiac arrhythmia treatments. With a strong focus on research and development, they provide cutting-edge tools that enable physicians to perform ablations with greater accuracy, reduce procedure times, and enhance patient care.
Their flagship products, incorporate advanced energy delivery and visualization techniques, making them unique in the electrophysiology space. These systems seamlessly integrate into existing clinical workflows, supporting electrophysiologists in treating complex cardiac conditions with confidence. The company is committed to advancing the treatment of AFib through innovation, providing both physicians and patients with effective solutions that drive better clinical results and improve quality of life.
Description The Design Quality Engineer, Medical Devices, will:
Lead Design Assurance activities throughout the product life cycle Provide expertise in Risk Management, Design Verification, and Validation (DV & V) Oversee Test Method Validation (TMV) and Process Validation (PV) activities Apply statistical methods to support product development and testing Utilize systematic problem-solving to address and resolve quality issues Stay current with regulatory requirements and standards for medical device development Guide and mentor engineering team members in Design Control processes Support complaint handling and Corrective and Preventive Actions (CAPA) as needed Ensure compliance with design controls throughout the product life cycle Contribute to the development and execution of validation plans Review and approve relevant documentation for design assurance activities Perform additional responsibilities as assigned by leadership
Profile BS in science or engineering with 5+ years of experience in quality management within the medical device or life sciences industry - experience as a Design Quality Engineer at a medical device manufacturer preferred Background in electrical engineering preferred, with experience in Class III medical devices and cardiac electrophysiology devices a plus Demonstrated leadership skills and the ability to manage teams to meet company objectives Strong problem-solving abilities, able to collect and organize diverse information to guide decisions and ensure product quality Experience in prioritizing and planning work, setting goals, and managing tasks for self and others Excellent written and verbal communication skills, with the ability to interact effectively across all organizational levels Deep knowledge of quality engineering principles, medical device requirements, and regulatory standards Ability to train and mentor others on quality engineering concepts and medical device compliance Familiarity with US FDA regulations, ISO standards, and applicable industry guidelines Experience in managing and improving quality systems and ensuring product compliance Strong organizational and planning skills to manage multiple projects concurrently Ability to identify and address gaps in quality processes to ensure continuous improvement Local to Westborough, MA Apply today for consideration of your application within 48 business hours!
Job Offer Medical Benefits : Great options available, allowing employees to select plans that best meet their needs. Dynamic Work Environment : Fast-paced and exciting atmosphere with a growing company. Career Growth : Opportunities to take on various roles and projects, gaining valuable experience. Recognition : Superiors value and appreciate employee contributions, providing a gratifying work experience. Company Culture : A supportive and positive work environment that fosters teamwork and individual success. Long-Term Outlook : Room for growth within the company, though potential future changes are a consideration.
MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.
Description The Design Quality Engineer, Medical Devices, will:
Lead Design Assurance activities throughout the product life cycle Provide expertise in Risk Management, Design Verification, and Validation (DV & V) Oversee Test Method Validation (TMV) and Process Validation (PV) activities Apply statistical methods to support product development and testing Utilize systematic problem-solving to address and resolve quality issues Stay current with regulatory requirements and standards for medical device development Guide and mentor engineering team members in Design Control processes Support complaint handling and Corrective and Preventive Actions (CAPA) as needed Ensure compliance with design controls throughout the product life cycle Contribute to the development and execution of validation plans Review and approve relevant documentation for design assurance activities Perform additional responsibilities as assigned by leadership
Profile BS in science or engineering with 5+ years of experience in quality management within the medical device or life sciences industry - experience as a Design Quality Engineer at a medical device manufacturer preferred Background in electrical engineering preferred, with experience in Class III medical devices and cardiac electrophysiology devices a plus Demonstrated leadership skills and the ability to manage teams to meet company objectives Strong problem-solving abilities, able to collect and organize diverse information to guide decisions and ensure product quality Experience in prioritizing and planning work, setting goals, and managing tasks for self and others Excellent written and verbal communication skills, with the ability to interact effectively across all organizational levels Deep knowledge of quality engineering principles, medical device requirements, and regulatory standards Ability to train and mentor others on quality engineering concepts and medical device compliance Familiarity with US FDA regulations, ISO standards, and applicable industry guidelines Experience in managing and improving quality systems and ensuring product compliance Strong organizational and planning skills to manage multiple projects concurrently Ability to identify and address gaps in quality processes to ensure continuous improvement Local to Westborough, MA Apply today for consideration of your application within 48 business hours!
Job Offer Medical Benefits : Great options available, allowing employees to select plans that best meet their needs. Dynamic Work Environment : Fast-paced and exciting atmosphere with a growing company. Career Growth : Opportunities to take on various roles and projects, gaining valuable experience. Recognition : Superiors value and appreciate employee contributions, providing a gratifying work experience. Company Culture : A supportive and positive work environment that fosters teamwork and individual success. Long-Term Outlook : Room for growth within the company, though potential future changes are a consideration.
MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.