Quality Technician

Responsibilities

• Perform receiving inspection of incoming raw materials using appropriate measurement tools and documentation practices.
• Prepare engineering and test samples to support product and process development activities.
• Record test results accurately and compare them against defined acceptance criteria, escalating issues when needed.
• Print and verify finished product labeling to ensure accuracy and compliance with requirements.
• Review and approve Product Lot Folders to confirm completeness, accuracy, and compliance with quality standards.
• Support equipment installation and qualification activities, including documentation and verification steps.
• Aid in the development of internal and supplier-based quality plans to improve product and process quality.
• Maintain and update Quality Management System (QMS) documentation in accordance with established procedures.
• Support Corrective and Preventive Action (CAPA) activities by gathering data, documenting findings, and assisting in implementation and verification of actions.
• Collaborate daily with Quality Engineering and other cross-functional teams to resolve quality issues and improve processes.
• Use micrometers, calipers, and other measurement tools to perform precise inspections and measurements.
• Manage multiple tasks and priorities in a dynamic environment, taking initiative and working with minimal supervision.

Essential Skills

• 2+ years of experience working in a Quality Technician role, preferably within the medical device industry.
• Hands-on experience performing receiving inspections of materials and components.
• Proficiency using micrometers, calipers, and other measurement tools for precise inspections.
• Strong documentation skills with the ability to record, organize, and maintain accurate quality records.
• Experience working within a Quality Management System (QMS) environment.
• Familiarity with CAPA (Corrective and Preventive Action) processes and supporting activities.
• Experience supporting validation and qualification activities for equipment and processes.
• Self-starter mentality with the ability to take initiative and manage multiple responsibilities.
• Strong collaboration skills and comfort working closely with engineers and cross-functional teams.

Additional Skills & Qualifications

• 2-year degree in a technical, scientific, or related field.
• Experience in the medical device industry, particularly in a manufacturing or quality environment.
• Ability to wear multiple hats and adapt to changing priorities in a growing organization.
• Comfort working in a smaller company setting with a lean management structure.
• Interest in expanding skills in QMS documentation, CAPA, validation, and quality planning.
• Ability to contribute to internal and supplier-based quality plan development.

Work Environment

The role is based in a small, growing company of roughly 60 people within a midsized organization that is expanding through acquisition. The culture emphasizes collaboration, self-motivation, and close daily interaction with engineers and cross-functional teams. The work environment is business casual and supports individuals who take initiative and enjoy learning new skills.

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 $20.00 - $33.00/hr.

Requirements

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)

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.

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.