Control Testing Jobs in Wisconsin (NOW HIRING)

This QC Laboratory Technician role focuses on performing routine and specialized laboratory testing on raw materials, in-process samples, finished goods, and stability samples for liquid-based pharmaceutical products in an FDA-regulated environment. You will support quality control operations by conducting wet chemistry analyses, maintaining laboratory equipment, and ensuring accurate documentation in accordance with standard operating procedures and good laboratory practices.

Responsibilities

• Perform laboratory testing on raw materials, in-process samples, finished products, and stability samples according to approved standard operating procedures.
• Conduct wet chemistry analyses, including titrations and other routine QC tests, to support the release and monitoring of liquid-based pharmaceutical products.
• Operate and perform testing using laboratory instruments such as FTIR, auto-titrators, pH meters, and analytical balances (scales).
• Read, interpret, and follow USP test methods, applying familiarity with USP requirements to perform identification and physical testing.
• Document all test data, observations, and calculations accurately and completely in accordance with data documentation procedures and good laboratory practices.
• Review test data, calculations, and results for accuracy, completeness, and compliance with specifications before reporting or submission.
• Maintain laboratory equipment by performing routine upkeep, identifying malfunctions, and carrying out simple repairs when appropriate.
• Coordinate equipment repairs with appropriate internal or external resources when issues exceed basic troubleshooting.
• Update and follow standard operating procedures related to laboratory testing, equipment use, and documentation as needed.
• Adhere to all laboratory safety procedures, including proper handling of chemicals and use of personal protective equipment.
• Balance laboratory testing activities (approximately 75% of the time) with administrative and paperwork tasks (approximately 25% of the time).
• Collaborate with QC personnel and interact with production staff or leadership as needed to support testing requirements and resolve quality-related questions.

• Basic laboratory experience in a quality control or similar laboratory environment, with the ability to perform routine tests and follow established procedures.
• Hands-on experience or training in wet chemistry techniques, including titration.
• Ability to perform laboratory testing using FTIR, auto-titrators, pH meters, and analytical balances, or the aptitude to learn these instruments quickly.
• Familiarity with USP test methods and the ability to read and apply USP procedures to identification and physical testing.
• Strong attention to detail and accuracy in recording data, performing calculations, and reviewing results.
• Understanding of and adherence to good laboratory practices and laboratory safety procedures.
• Ability to maintain and troubleshoot basic laboratory equipment and recognize when to escalate issues for repair.
• Effective organizational skills to manage both laboratory work and administrative or documentation tasks.
• Ability to work a second-shift schedule after completion of training on first shift.

• Degree in a scientific discipline such as Biology, Chemistry, Biochemistry, or a related field is preferred.
• Experience in laboratory testing, particularly in QC chemistry, is beneficial.
• Background or coursework in biology, chemistry, or biochemistry that supports understanding of laboratory methods and product testing.
• Experience with wet chemistry and titration techniques in an academic or professional setting.
• Ability to learn and adapt to new laboratory methods, instruments, and standard operating procedures.
• Strong communication skills to collaborate effectively with QC personnel and other departments.

This position is based in a QC Chemistry Laboratory that supports testing of FDA-regulated, liquid-based pharmaceutical products. The role involves working approximately 75% of the time in the laboratory performing hands-on testing and about 25% of the time in an office setting handling documentation and administrative tasks. The standard schedule for the role is on second shift, working four 10-hour days from Monday through Thursday, approximately 3:30 p.m. to 1:30 a.m. Initial training will take place on first shift for about four weeks, Monday through Friday, typically from 8:00 a.m. to 5:00 p.m., before transitioning to the second-shift schedule. The environment is business casual, with appropriate laboratory attire and personal protective equipment required while working in the lab. You will work primarily with QC personnel and may occasionally interact with production staff and leadership to support testing and quality activities.

Job Type & Location

This is a Contract to Hire position based out of HARTLAND, WI.

The pay range for this position is $21.00 - $25.00/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)

This is a fully onsite position in HARTLAND,WI.

This position is anticipated to close on Jul 10, 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.

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