Quality Manager
Company: Actalent
Location: Sturtevant
Posted on: February 20, 2026
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Job Description:
Job Description Job Description Job Title: Quality Manager Job
Description The Quality Manager will play a pivotal role in
ensuring customer product specifications, standards, and regulatory
requirements are met by supervising quality technicians. This
position requires effective communication with customers regarding
issues, requests, and new product introductions, as well as hosting
customer and regulatory audits. Responsibilities Prioritize,
schedule, and delegate work assignments to quality technicians.
Ensure conformance to customer product specifications, standards,
and regulatory requirements. Host customer and regulatory audits.
Manage the material review board process, part production approval
process (PPAP), first article inspection, internal audit schedule,
quality team’s work hours, calibration schedule, quality control
plans, and receiving inspection. Oversee the review and creation of
control plans on prototype builds. Establish and implement quality
procedures, specifications, testing procedures, and standards for
raw materials for in-process and finished products. Process
customer returns and facilitate closure of non-conformance cases
with the customer. Develop training curriculum and train employees
in quality-related practices and system requirements. Analyze
internal and customer return/complaint data to identify corrective
and preventive actions. Participate in cross-functional teams to
support continuous improvement projects to improve levels of
quality and productivity. Coach problem-solving techniques such as
5 why, fishbone, pareto, and 8D method. Utilize six sigma methods
to analyze process and measurement variation, including capability
study and gauge reproducibility and repeatability. Manage
complaints, CAPA, and non-conforming products per applicable
ISO13485 and FDA requirements. Manage inputs and KPI metrics for
management review process per ISO13485 and FDA requirements.
Maintain Medical Device Files and records per ISO requirements.
Essential Skills Quality assurance CAPA Audit Medical device
Confidence going through an FDA audit 5-10 years of experience in
Quality in Medical Device 3-5 years of management experience
Additional Skills & Qualifications BS Degree Preferred experience
working within a small company, as the individual will wear many
hats. Work Environment The position operates in a manufacturing and
office setting, with standard first shift hours. The role offers
flexibility for childcare needs. The company is looking to grow 3-5
times in the next 5 years, providing opportunities for future
leadership growth. Job Type & Location This is a Permanent position
based out of Sturtevant, WI. Pay and Benefits The pay range for
this position is $95000.00 - $120000.00/yr. MPE, Inc. in Wisconsin
offers a comprehensive internal benefits package that includes
medical, dental, and vision insurance, along with life and
disability coverage for employees. Employees also have access to
retirement benefits such as a 401(k) plan with company matching
and, in some roles, profit sharing. Paid time off, paid holidays,
and paid jury duty are part of MPE’s standard benefits, supporting
work–life balance. Additional benefits noted in postings include
health savings accounts, tuition reimbursement, and an employee
assistance program, reflecting an emphasis on both financial and
personal well-being. Workplace Type This is a fully onsite position
in Sturtevant,WI. Application Deadline This position is anticipated
to close on Feb 28, 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 the modification or adjustment of the job
application process or interviewing due to a disability, please
email actalentaccommodation@actalentservices.com for other
accommodation options.
Keywords: Actalent, Gary , Quality Manager, Engineering , Sturtevant, Indiana