Quality Assurance Technician

Quality Assurance Specialist

The Quality Assurance Specialist supports production quality in a regulated manufacturing environment and ensures strict compliance with established standards and procedures. This role focuses on documentation review, product release, changeover oversight, and issue escalation, rather than routine production line checks. The position plays a key part in launching and sustaining new product lines by establishing and reinforcing quality and sensory standards.

Responsibilities

• Create and manage work orders and complete all related documentation in alignment with the production schedule.
• Maintain product retains, including collection, tracking, organization, and secure storage.
• Issue deviations, document nonconformances, and partner with Quality Assurance to investigate and resolve issues.
• Address on-floor and quality control inspection concerns, including labeling accuracy, component placement, and overall product quality.
• Inspect and approve incoming components and evaluate questionable parts, escalating concerns when necessary.
• Establish sensory standards for finished goods and train production and quality staff on these standards.
• Review batch records for completeness and accuracy and provide second sign-off for product release.
• Complete changeover documentation for production runs to ensure proper line clearance and compliance with procedures.
• Maintain accurate quality records and tracking systems to support audits and continuous improvement initiatives.
• Drive continuous improvement by identifying quality issues, reinforcing standards, and recommending process enhancements.
• Perform inspections using tools such as micrometers, calipers, pin gauges, and placement gauges as required.
• Visually compare colors against established reference standards and identify color-coded labels, status tags, and chemical hazard warnings.
• Evaluate the appearance of raw materials and finished products to identify irregularities or deviations from established specifications.
• Detect and differentiate odors during evaluation of raw materials and finished products in accordance with applicable testing specifications, including identifying unexpected or out-of-specification odors.
• Collaborate effectively with production, quality, and R&D teams to support new product lines and ensure robust quality testing.
• Adapt to changing priorities and production schedules while maintaining high quality standards and meeting deadlines.

Essential Skills

• 1–3 years of quality assurance experience in a manufacturing or regulated environment.
• Direct experience in Quality Assurance activities such as reviewing documentation, managing product release, completing changeover documents, and serving as an escalation point when issues arise.
• Experience working with regulated products such as food, cosmetics, personal care, over-the-counter products, coatings, or similar environments.
• Working knowledge of FDA regulations, GMP (Good Manufacturing Practices), GDP (Good Documentation Practices), and quality systems.
• Experience using inspection tools including micrometers, calipers, pin gauges, and placement gauges.
• Strong attention to detail with the ability to identify deviations and maintain accurate documentation.
• Excellent organizational skills and the ability to prioritize and multitask in a dynamic production environment.
• Proficiency in Microsoft Word, Excel, and basic computer systems.
• Strong communication and interpersonal skills with a collaborative, team-oriented mindset.
• Ability to adapt to changing priorities and production schedules while maintaining compliance with quality standards.
• Ability to perform tasks requiring close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
• Ability to visually compare colors against reference standards and accurately identify color-coded labels, status tags, and hazard warnings.
• Ability to detect and differentiate odors during evaluation of raw materials and finished products, including identifying out-of-specification odors.
• Ability to visually evaluate the appearance of raw materials and finished products and identify irregularities or deviations from standards.

Additional Skills & Qualifications

• Associate or technical degree in a relevant field is preferred.
• Experience in environments such as food, pharmaceutical, cosmetics, chemical, or other regulated manufacturing sectors.
• Familiarity with laboratory practices, bacteria culture, and aseptic technique.
• Experience working with GMP-compliant processes and laboratory-based quality testing.
• Comfort working with standard operating procedures (SOPs), work orders, QC inspections, sensory standards, and batch records.
• Interest in supporting new product lines for lotions, creams, personal care, and over-the-counter products as part of a growing operation.
• Eligibility for paid time off benefits, including billable PTO and holidays, in accordance with company policies.

Work Environment

This role is based in a manufacturing facility and involves both office-based documentation work and on-floor activities in production and laboratory areas. The Quality Assurance Specialist will perform plant sampling as needed in the manufacturing space and will regularly interact with production, quality, and R&D teams. The position follows a Monday–Friday schedule from 12:00 p.m. to 8:30 p.m. The environment includes exposure to raw materials, finished products, and testing equipment, and requires the ability to visually assess color, appearance, and labeling as well as detect and differentiate odors. The facility operates under FDA, GMP, and quality system standards, with a focus on supporting new lotions, creams, personal care, and OTC product lines and expanding R&D processes to ensure robust quality testing.

Job Type & Location

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

Pay and Benefits

The pay range for this position is $20.00 - $26.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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 Type

This is a fully onsite position in Chanhassen, MN.

Application Deadline

This position is anticipated to close on Sep 14, 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 View email address on click.appcast.io 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.