Job Description
This role focuses on manufacturing and testing calibration materials used in diagnostic medical equipment for hospitals and clinics. You will prepare reagents and solutions, operate analytical instruments, and ensure all products meet strict quality and regulatory standards. The position is ideal for a science graduate with hands-on manufacturing lab experience who enjoys independent, detail-oriented work in a regulated environment.
Responsibilities
- Prepare calibration materials, buffers, and reagents used in diagnostic medical equipment according to established procedures and specifications.
- Apply analytical and scientific methods to daily tasks, including accurate pipetting and handling of laboratory materials.
- Set up, calibrate, operate, and troubleshoot DXI800 and DXI19000 instruments to support production activities.
- Perform functional testing on reagent components and instruments to verify performance and ensure products meet required specifications.
- Conduct testing on solutions, including pH, conductivity, and density measurements, to confirm adherence to production and process specifications.
- Follow and interpret Standard Operating Procedures (SOPs) for all laboratory and production processes related to calibrator manufacturing.
- Document test results, production data, and any deviations accurately in accordance with regulatory and internal quality requirements.
- Investigate and document non-conformances, participate in Corrective and Preventive Actions (CAPAs), and support scheduling and inventory-related tasks.
- Ensure compliance with FDA Quality System Regulations (QSR) and Good Manufacturing Practices (GMP) in all work activities.
- Collaborate with team members while working independently to manage daily workload, prioritize tasks, and resolve technical issues.
- Use computer-based tools for data analysis, trending, and verification to ensure that all products meet defined specifications.
- Support continuous improvement of processes by seeking out answers, identifying issues, and proposing solutions within the regulated manufacturing environment.
- Bachelor's degree in a science-related field.
- At least 12 months of manufacturing laboratory experience.
- Demonstrated experience following Standard Operating Procedures (SOPs) and documenting work accurately.
- Proven ability to work independently, as verified by references or prior experience.
- Strong pipetting skills and experience with routine laboratory techniques.
- Ability to apply analytical skills and scientific methods to daily laboratory and production tasks.
- Experience performing solution testing such as pH, conductivity, and density measurements.
- Familiarity with working in a regulated manufacturing or production environment.
- Ability to troubleshoot laboratory instruments and processes, including calibration and basic maintenance activities.
- Strong initiative and ability to seek out answers and resources to resolve issues.
- Comfort with computer-based work, including data entry, data analysis, and use of laboratory or production software.
- Prior experience in a manufacturing laboratory environment beyond the minimum requirement.
- Good Manufacturing Practices (GMP) experience.
- Experience working under FDA Quality System Regulations (QSR) or similar regulatory frameworks.
- Hands-on experience with chemistry-based laboratory processes, particularly in reagent preparation and formulation.
- Exposure to non-conformance investigations and participation in Corrective and Preventive Actions (CAPAs).
- Experience with scheduling and inventory-related tasks in a production or laboratory setting.
- Familiarity with operating and maintaining diagnostic or analytical instruments such as DXI800 and DXI19000.
- Strong communication skills and ability to clearly articulate previous experience and adherence to SOPs.
This position operates on a first-shift schedule, typically 8:00 a.m. to 4:30 p.m., Monday through Friday, with flexibility to start or end the day earlier or later as needed. The role is based in a regulated manufacturing and production environment focused on developing, manufacturing, and marketing products that simplify, automate, and innovate complex biomedical testing. Approximately 70% of your time will be spent in the laboratory performing direct labor activities such as making buffers, preparing materials, pipetting, running functional tests on analytical instruments, and following SOPs for calibrator production. The remaining 30% involves activities such as handling non-conformances, supporting CAPAs, managing scheduling tasks, and maintaining inventory, along with computer-based work and data analysis to ensure specifications are met. You will work primarily in a large, chemistry-based main lab with access to modern analytical equipment and production systems. The work is highly independent, with clear procedures and quality expectations. The campus is located near a lake with walking trails between buildings and is conveniently situated close to local shops, restaurants, and a short drive from a major metropolitan area, providing a pleasant and accessible work setting.
Job Type & Location
This is a Contract to Hire position based out of Chaska, MN.
Pay and BenefitsThe pay range for this position is $28.00 - $30.00/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 Chaska,MN.
Application DeadlineThis position is anticipated to close on Jun 3, 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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-006038074
