Quality Technician
Actalent, Saint Paul, MN, United States
Job Title: Quality Technician
The Quality Technician supports the design, development, and manufacture of advanced hemostat and wound healing technologies by performing hands‑on quality activities in a collaborative, team‑based environment. This role works closely with Operations, Quality, and Engineering teams, focusing approximately 25% of the time on receiving inspection and 75% on broader quality functions such as QMS documentation, CAPA support, and validation activities. The position is ideal for a self‑motivated individual who enjoys working in a small, growing organization and is eager to expand their skills and responsibilities.
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.
Assist 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.
Ability to support 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
Preferred 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. Typical hours are approximately 8:00 a.m. to 4:30 or 5:00 p.m. The company offers 120 hours per year of accrued paid time off, additional state safe and sick time, and 8 paid holidays. The setting involves working with quality and measurement tools, supporting production and engineering activities, and engaging in both office‑based documentation work and hands‑on inspection tasks.
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.
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 Type
This is a fully onsite position in Saint Paul, MN.
Application Deadline
This position is anticipated to close on May 8, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self‑reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
#J-18808-Ljbffr
The Quality Technician supports the design, development, and manufacture of advanced hemostat and wound healing technologies by performing hands‑on quality activities in a collaborative, team‑based environment. This role works closely with Operations, Quality, and Engineering teams, focusing approximately 25% of the time on receiving inspection and 75% on broader quality functions such as QMS documentation, CAPA support, and validation activities. The position is ideal for a self‑motivated individual who enjoys working in a small, growing organization and is eager to expand their skills and responsibilities.
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.
Assist 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.
Ability to support 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
Preferred 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. Typical hours are approximately 8:00 a.m. to 4:30 or 5:00 p.m. The company offers 120 hours per year of accrued paid time off, additional state safe and sick time, and 8 paid holidays. The setting involves working with quality and measurement tools, supporting production and engineering activities, and engaging in both office‑based documentation work and hands‑on inspection tasks.
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.
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 Type
This is a fully onsite position in Saint Paul, MN.
Application Deadline
This position is anticipated to close on May 8, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self‑reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
#J-18808-Ljbffr