At least 6 years
The Quality Engineer owns and drives Corrective and Preventive Action (CAPA) activities end-to-end, manages Non-Conforming Material Reports (NCMRs), and supports design quality across the product lifecycle with a focus outside manufacturing operations. This role operates with a strong sense of urgency to resolve quality events, identifies and addresses gaps in quality processes, and collaborates closely with Engineering, Regulatory, and Operations teams to improve product quality and patient outcomes. The position offers the opportunity to take ownership of quality initiatives, build and refine processes, and grow within a collaborative, mission-driven environment.
Responsibilities- Own and drive CAPA activities from initial investigation through root cause analysis, implementation of corrective and preventive actions, and formal closure.
- Manage and resolve Non-Conforming Material Reports (NCMRs), ensuring appropriate disposition and documentation.
- Support design quality efforts across the product lifecycle, with a primary focus on activities outside of manufacturing operations.
- Collaborate cross-functionally with Engineering, Regulatory, and Operations to investigate and resolve quality issues and ensure alignment on quality standards.
- Identify gaps in existing quality processes and proactively propose, develop, and implement improvements.
- Operate with a strong sense of urgency to ensure timely resolution of quality events and minimize impact on products and patients.
- Balance hands-on execution and effective delegation, while remaining directly involved in technical quality work as needed.
- Independently manage quality investigations and CAPA tasks with limited direction, maintaining high standards of documentation and compliance.
- Support both technical execution and process ownership for quality systems and initiatives.
- Contribute to building and refining quality processes in a fast-paced, evolving environment.
- 2–6+ years of experience in Quality Engineering within medical devices or a regulated industry.
- Hands-on experience independently managing CAPAs and conducting quality investigations.
- Experience working with Non-Conforming Material Reports (NCMRs).
- Exposure to design quality principles, with focus not strictly limited to manufacturing or operations.
- Strong problem-solving skills and the ability to think critically through complex quality issues.
- Proven ability to work independently with limited direction while maintaining accountability for results.
- Excellent communication skills, with the ability to clearly convey technical information to cross-functional partners.
- Demonstrated cross-functional collaboration skills with Engineering, Regulatory, and Operations teams.
- Comfort working in fast-paced, evolving environments with a degree of ambiguity.
- Demonstrated ability to quickly ramp up and hit the ground running in new roles.
- Experience working in a Contract Manufacturer (CMO) or small to mid-sized medical device company.
- Prior experience supporting both technical execution and ownership of quality processes.
- Motivation to build and improve quality processes in a growing, innovative organization.
- Interest in contributing to product quality and patient outcomes in a mission-driven setting.
- Ability to balance detailed technical work with broader process improvement initiatives.
- Eligibility for equity upon full-time conversion, subject to company policies.
The role is based in a growing, innovative medical device environment that is fast-paced and evolving, with a culture that values ownership, collaboration, and mission-driven work focused on improving patient outcomes. The team operates with core collaboration hours from 9:00 AM to 3:00 PM, offering flexibility outside of those hours to support work-life balance. You will work closely with Engineering, Regulatory, and Operations in a highly cross-functional setting, with an emphasis on both technical quality execution and continuous process improvement. The organization uses a work model designed to ensure mutual fit, allowing you to grow into full-time opportunities and potentially participate in equity programs upon conversion.
Job Type & LocationThis is a Contract to Hire position based out of Saint Paul, MN.
Pay and BenefitsThe pay range for this position is $45.00 - $60.00/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 TypeThis is a fully onsite position in Saint Paul,MN.
Application DeadlineThis position is anticipated to close on Aug 5, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
Posting ID: JP-006172822