<p>Job Title: Quality Engineer</p> <p>Job Description</p> <p>We are seeking a talented Quality Engineer experienced with internal or external auditing to ensure compliance with internal Quality Management System (QMS) requirements. The ideal candidate should have a solid understanding of 21 CFR 820 and Current Good Manufacturing Practice (CGMP) regulations. This position is a 2-year contract located in Plymouth, MN.</p> <p>Responsibilities</p> <ul> <li>Understand detailed QMS requirements. </li><li>Review product and QMS documentation to evaluate compliance. </li><li>Maintain an internal audit schedule. </li><li>Assist in communicating internal audit agendas and scheduling. </li><li>Participate in internal audits. </li><li>Generate Internal Audit reports. </li><li>Review and approve product and QMS work products as required. </li><li>Perform general quality engineering tasks. </li></ul> <p>Essential Skills</p> <ul> <li>Experience with internal or external auditing. </li><li>Understanding of 21 CFR 820 regulations. </li><li>Knowledge of CGMP regulations. </li><li>Experience in quality engineering, particularly in the medical device sector. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Quality Engineer qualification. </li></ul> <p>Work Environment</p> <p>This role requires working on-site at 1405 Xenium Ln N, Suite 150, Plymouth, MN, USA, 55441. The position is for 40 hours per week, with a standard schedule of 8 hours per day starting on Monday. The work environment is technical and part of the Quality - Multi-Division business unit. The role requires onshore work and does not allow for remote or virtual work options.</p> <p>Job Type & Location</p> <p>This is a Contract position based out of Minneapolis, Minnesota.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $35.00 - $37.00/hr.</p> <p>Eligibility requirements apply to some benefits and may depend on your job</p> <p>classification and length of employment. Benefits are subject to change and may be</p> <p>subject to specific elections, plan, or program terms. If eligible, the benefits</p> <p>available for this temporary role may include the following:</p> <ul> <li>Medical, dental & vision </li><li>Critical Illness, Accident, and Hospital </li><li>401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available </li><li>Life Insurance (Voluntary Life & AD&D for the employee and dependents) </li><li>Short and long-term disability </li><li>Health Spending Account (HSA) </li><li>Transportation benefits </li><li>Employee Assistance Program </li><li>Time Off/Leave (PTO, Vacation or Sick Leave) </li></ul> <p>Workplace Type</p> <p>This is a fully onsite position in Minneapolis,MN.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Sep 6, 2025.</p> <p>About Actalent</p> <p>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.</p> <p>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.</p> <p>If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.</p>