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Senior Quality Engineer

Job in Maple Grove, Hennepin County, Minnesota, 55311, USA
Listing for: Actalent
Full Time position
Listed on 2026-01-13
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 90000 USD Yearly USD 90000.00 YEAR
Job Description & How to Apply Below

Senior Quality Engineer

Actalent is looking for a Senior Manufacturing Quality Engineer to join our innovative team working on cutting‑edge technologies in cardiology. This role focuses on ensuring design assurance for a heart valve and a delivery catheter system.

Job Description

The Senior Manufacturing Quality Engineer is a key member of our innovative team working on cutting‑edge technologies in the field of cardiology. The primary responsibility of this role is to ensure the design assurance of a heart valve and a delivery catheter system. This position requires a background in the medical device industry, particularly in cardiological devices, including implantable heart valves and transcatheter delivery systems, along with a strong understanding of regulations and standards such as 21 CFR 820.

Responsibilities
  • Lead the product development process including key design assurance activities, design reviews, verification and validation activities, development and validation of testing methods, management of product requirements, test case tracing, and risk management.
  • Facilitate the transition of new product development into production.
  • Conduct reviews and enhancements of Quality Management System (QMS) processes related to design controls and design assurance activities.
  • Gather, analyze, and present data using statistical tools and other analytical methodologies.
  • Engage actively with team members, contributing to discussions with strong verbal and written communication skills.
  • Demonstrate adaptability for rapid iteration and flexibility in design and strategy changes.
Essential Skills
  • Minimum of a Bachelor’s degree in a technical field or equivalent professional experience.
  • 8+ years of experience in the medical device industry with 3 to 5 years in Quality.
  • Deep understanding of CE Marking, EU MDR, FDA Medical Device Regulation (MDR), and FDA requirements.
  • Extensive knowledge of manufacturing processes and practices relevant to the company’s products.
  • Proficiency in Microsoft Office applications including Excel, Word, and Outlook.
  • Ability to work collaboratively across all organizational levels.
  • Strong leadership skills to manage subordinates, projects, and workflow effectively.
Additional

Skills & Qualifications
  • Meticulous attention to detail, strong analytical skills, and robust problem‑solving capabilities.
  • Superior communication skills and the capacity to collaborate effectively within a team setting.
  • Experience in CAPAS functions, risk management, verification, and validation aligned with industry standards.
  • Knowledge in statistics, data collection, analysis, and presentation techniques.
  • Ability to handle confidential and sensitive information with professionalism.
  • Exhibits exceptional organizational skills and the ability to prioritize multiple tasks.
Work Environment

The position is based on‑site in Maple Grove, MN, within a small culture‑oriented team that values collaboration and innovation. The work environment is dynamic and fast‑paced, requiring multitasking and adaptability to evolving needs.

Job Type & Location

Permanent position based out of Maple Grove, MN.

Pay And Benefits

Pay range: $90,000.00 – $ per year.

Benefits include medical, dental, vision plans effective from hire date;
Health Care Savings Account (HSA);
Employee Stock Ownership Program (ESOP);
Company‑Paid Long‑Term Disability (LTD);
Paid Parental Leave;
Paid Bereavement Leave;
Paid Time Off;
Paid Holidays;
Employee Assistance Program.

Workplace Type

Fully onsite in Maple Grove, MN.

Final date to receive applications

Position anticipated to close on Jan 23, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal‑opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccom for other accommodation options.

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Position Requirements
10+ Years work experience
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