As a QC Technician I, you will perform essential tasks following established procedures and work instructions. Your role will involve performing microbiological tasks such as inoculations, maintaining stock, dilutions, gram stains, and conducting physical assessments of finished and intermediate samples. You will gain proficiency in all technician testing areas and ensure the accurate and consistent documentation of inspection results. Your responsibilities will also include maintaining consistency in training tasks, conducting daily calibrations of measuring equipment, and ordering necessary consumable stock supplies. Compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) is essential, and you will work effectively in a high-volume, fast-paced environment while collaborating closely with the Quality Assurance department.
ResponsibilitiesPerform microbiological tasks including inoculations, maintaining stock, dilutions, gram stains, and physical assessments of samples.Gain proficiency in all technician testing areas.Document inspection results accurately and consistently.Conduct daily calibrations of measuring equipment within the QC laboratory.Order consumable stock supplies when necessary.Exercise compliance with GMP and GLP in the work environment.Collaborate closely with the Quality Assurance department.Participate in the continuous improvement program within the department.Understand and adhere to all safety requirements and procedures.Assist in maintaining standards in accordance with GMPs, SOPs, and ISO regulations.Support department and company goals.Adhere to and support all company policies.Perform other duties as assigned.
Essential SkillsMicrobiology knowledgePossess at least an Associate's degree in Biology.1-2 years of experience in QC/QA, microbiology laboratory work, or equivalent combination of education and experience.Ability to manage multiple tasks in an organized manner.Intermediate computer skills, including Microsoft Word, Excel, and PowerPoint.Experience in SAP is a plus.
Additional Skills & QualificationsLaboratory experience in a biological sciences laboratory is preferred.Previous experience working in an FDA-regulated environment is preferred.Self-motivated.
Work Environment
The work schedule is Friday to Monday from 7 AM to 5:30 PM (Weekend). You will be working in a high-volume, fast-paced environment that requires adherence to safety procedures and company policies.
Job Type & Location
This is a Contract position based out of Lenexa, Kansas.
Pay and Benefits
The pay range for this position is $20.00 - $20.00/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)
Workplace Type
This is a fully onsite position in Lenexa,KS.
Application Deadline
This position is anticipated to close on Sep 23, 2025.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.