Quality Engineer
Listed on 2026-01-15
-
Engineering
Quality Engineering, Process Engineer -
Quality Assurance - QA/QC
Quality Engineering
Job Description
We are seeking a passionate Quality Engineer to join our team, where you will play a pivotal role in driving excellence across product development and manufacturing. In this dynamic position, you will lead key initiatives such as part validation, qualification, and support for sustaining programs. You will also be the primary expert for addressing customer quality concerns, collaborating closely with both production and engineering teams to ensure the highest standards are met consistently.
Responsibilities- Participate in the organization’s overall Stage-Gate approach to product realization.
- Manage APQP and PPAP activities for new and modified programs as directed by the Quality & Regulatory Manager.
- Conduct Quality Planning, including Process Flow Diagrams, Process FMEA, and Process Control Plan.
- Prepare work instructions and inspection instructions.
- Oversee PPAP/validation for purchased materials and components.
- Implement and report on Pre-Launch/early containment activities.
- Enhance relationships and the company’s position with customers and suppliers through direct interface and strong leadership.
- Make decisions on materials placed on-hold internally.
- Participate in the creation and management of CAPAs, SCARs, RMA activities, and sustaining programs.
- Write and issue Quality Alerts.
- Write and perform validation protocols.
- Collaborate with customers and employees to provide consultation and advice on quality issues.
- Serve as the primary contact for quality issues for assigned customers as directed by the Quality Assurance Manager, which may include visiting customer locations.
- Conduct training related to the Quality Management System as needed.
- Bachelor's Degree or equivalent work experience.
- Valid identification and the ability to work legally in the United States.
- Four years of experience in a regulated manufacturing environment.
- Proficiency in APQP, PPAP, and SPC.
- Experience with ISO
9001, ISO
13485, or FDA certifications. - Familiarity with Epicor or similar ERP systems.
- Experience in print reading, and cosmetic specifications.
- Ability to manage multiple projects concurrently.
- Excellent verbal and written communication skills with proficiency in Microsoft Suite.
- Experience with change control, revision control, and documentation.
Permanent position based out of Saint Paul, MN.
Pay range: $85,000 – $100,000 per year. Benefits include Medical, Dental, Vision, 401(k) with employer match, STD/LTD, Pet Insurance, Tuition Reimbursement, Gym Reimbursement, 3 weeks accrued PTO, and 9 paid holidays.
Workplace TypeFully onsite position in Saint Paul, MN.
Final date to receive applicationsAnticipated to close on Jan 23, 2026.
About ActalentActalent 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 actalentaccom for other accommodation options.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).