About ECI

ECI’s mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives and decades of expertise to tackle their toughest challenges and we take pride in providing them transformative solutions with distinctive, sustainable and long-term value. ECI boasts a proven track record of providing full product life cycle consulting on a variety of challenging and exciting projects. Our collaborative culture, welcoming team and flexible employment & benefit options allow us to maintain strong relationships with the most talented individuals in the life sciences industry.

About the role
As Senior R&D Engineer you will support the DHF remediation activities for our client’s division.   

What you will do
Support design history file remediation activities associated with the client’s division, including as needed but not limited to: Design Inputs, Design Outputs, Design Verification, Design Validation   and Risk Management  

Interface with client’s team members along with coordinating activities within our client’s Quality Management System  

Additional items discussed between client and ECI as determined reasonably will not require scope re-evaluation. Product lines associated with the division and design history file documentation creation, updates, and approval within the client’s documentation management system.

Develops new products and or sustains current products including single use devices, and capital equipment devices with software and hardware (medical device systems) with minimal supervision to develop, maintain or improve current released device design and/or quality. Support team to develop and executes plans for a design and development/design change projects following design control requirements

What you will bring
Bachelor’s Degree in Engineering or equivalent work experience

Minimum of 5 (Five) years direct R&D experience in medical device industry

Experience with durable medical capital equipment in addition to single-use-devices is preferred

Excellent written and verbal communication skills with good presentation and technical writing skills

Collaborative attitude with the ability to work well in a team environment

Strong engineering, design, and analysis skills along with experience with medical devices from concept to commercialization

Understanding of FDA Quality Systems Regulations

Please apply online at Careers | ECI | Enhanced Compliance Inc. Req #4894

Expertise. Passion. Accountability.

At ECI, we employ passionate professionals who understand why we do what we do. We engage individuals eager to explore their own potential, relish the process of continual learning, and embrace challenges with enthusiasm.

Our collaborative team engages with industry trailblazers seamlessly merging science, technology, and a profound understanding of compliance regulations across diverse projects. The outcomes of our endeavors—innovative, life-changing, and life-saving advancements—positively impact people's lives. Join us to nurture your career growth at ECI.

ECI is an equal opportunity employer.

All qualified applicants will receive consideration for employment at ECI without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law.

At the time of this posting, all candidates must be authorized to work in the U.S. without the need for employment-based visa sponsorship now or in the future.  At the time of this posting, ECI will not sponsor applicants for U.S. work visa status for this opportunity.