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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.

Essential Skills:

+ 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 ISO9001, ISO13485, or FDA.

+ Familiarity with Epicor or similar ERP systems.

+ Experience in print reading, cGMP/GDP, GD&T, 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 change, and documentation.

Job Type & Location

This is a Contract to Hire position based out of Saint Paul, MN.

Pay and Benefits

The pay range for this position is $85000.00 - $100000.00/yr.

Medical Dental Vision 401k with employer match STD/LTD Pet Insurance Tuition Reimbursement Gym Reimbursement 3 Weeks Accrued PTO, 9 paid Holidays

Workplace Type

This is a fully onsite position in Saint Paul,MN.

Application Deadline

This position is anticipated to close on Jan 20, 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 [email protected] (%[email protected]) for other accommodation options.