About this opportunity
Enhanced Compliance Inc. lists this Senior R&D Engineer - Medical Device #9058 opportunity in arden hills, Minnesota. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Employee Type Contractor or FT Employee
Required Degree 4 Year Degree
Description
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 with 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.
What You’ll Do
Provide quality and compliance input to project teams for decisions and deliverables (e.g., Design Change Analysis, Design Inputs, Design Outputs, Test Methods, Design Review, Design V&V, Usability Testing, Process Validation, and Labeling)
Develop quality documentation such as quality plans, standard operating procedures, and inspection procedures. Ensure regulatory, FDA, and ISO compliance in all areas of responsibilities
Represent Quality initiatives and compliance when participating and Design and Phase reviews
Serve as an effective leader and team member in supporting quality disciplines, decisions, and practices
Ensure that required standards for products are documented in the product requirements (PR) specification and ensure compliance by performing quarterly gap analysis and reviewing applicable verification documentation
Ensure the use of statistically valid sampling techniques and teach others on the use of these and other advanced statistical techniques such as DOE and ANOVA evaluations
Provide direction and lead the implementation of Acceptance Activities, First Article Inspections, In-Process Inspections, Sampling Plans, product/component testing, inspections, and acceptance criteria
Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
Provide support for CAPA/NCRs/Complaints
Assist in special proj ect as needed or requested
What We Look For
Minimum of 5-6 years’ direct R&D experience in medical device industry working with electromechanical devices
Prior experience working with Cardiac Pacemaker, associated monitoring systems and battery, Class III FDA
Experience with durable medical capital equipment in addition to single-use devices is preferred
Excellent written and verbal communication skills with good presentation and t echnical 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
Demonstrated use of quality tools and methodologies including SPC, DOE, GR&R, FMEA, CAPA, and process validation (IQ, OQ/PQ)
Must have a good understanding of FDA 21CFR820, ISO 13485, 14971, and 11607 standards
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.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.