Job Description
We are seeking a dedicated Quality Assurance Associate to execute investigations, conduct root cause analysis, and manage corrective and preventive action activities. The successful candidate will work within our established Quality System to capture data related to product deviations, non-conformances, and rework, using this information to drive quality improvements.
ResponsibilitiesExecute investigations, root cause analysis, and corrective and preventive action activities in accordance with the Quality System for NCRs and CAPAs.Capture and analyze data associated with product deviations, non-conformances, CAPAs, scrap, and rework.Support change control activities by originating and reviewing internal operating procedures and specifications through the Document Change process.Assist with adherence to all Federal, State, and Local Regulations controlling the manufacture of medical devices.Essential SkillsProficiency in quality assurance processes and practices.Experience with FDA, GMP, GLP, and medical device regulations.Strong technical writing and problem-solving skills.Ability to manage multiple priorities and work with interruptions.Additional Skills & QualificationsBS in a Physical Science or Engineering or equivalent experience.Experience in Quality Assurance or other regulated industries is preferred.Strong customer service skills.Proficiency in Excel.Work Environment
The position operates on a first shift from 7am to 3:30pm, Monday through Friday, with the possibility of an additional hour per day. Candidates may occasionally be required to work 4 hours on Saturdays, typically on a voluntary basis. The work culture is family-oriented, fostering a team spirit where colleagues support one another. The company is dynamic, and candidates should be comfortable adapting to constant and sudden changes.
Pay and Benefits
The pay range for this position is $21.00 - $21.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Sturtevant,WI.
Application Deadline
This position is anticipated to close on Aug 8, 2025.
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 the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.