Microbiology Quality Control Technician III

Actalent; Lenexa (KS); On-site; USD 57,308,000 - 65,904,000; Part time

Job summary

Actalent is seeking a Microbiology - Quality Control Technologist in Lenexa, KS to ensure products meet quality, safety, and regulatory standards by conducting laboratory testing and maintaining GMP/GLP-compliant documentation.

This contract role involves collaborating with QA, following SOPs, and contributing to continuous improvement while adhering to safety protocols in a fast-paced lab.

Qualifications

• Quality control or QA experience in a laboratory setting.
• Microbiology laboratory experience preferred.
• Familiarity with GMP/GLP/ISO regulations.
• Experience with documentation control and quality records.

Responsibilities

• Review and maintain product compliance specifications and ensure all documentation remains accurate and controlled.
• Perform laboratory tests according to SOPs and record results per GMP/GLP/ISO.
• Document testing results with data, observations, and conclusions.
• Evaluate aesthetic quality of finished products against defined standards.
• Maintain training records in Master Control or similar systems.
• Adhere to SOP criteria for inspection and testing activities.
• Ensure GMP/GLP compliance in all testing processes.
• Collaborate with Quality Assurance to resolve issues and support quality initiatives.
• Participate in continuous improvement programs within the department.
• Follow all safety requirements and handling procedures.

Skills

Quality control

Microbiology lab

FDA regulations

Multitasking

Adaptability

Teamwork

Detail oriented

Tools

Master Control

Job description

Microbiology - Quality Control Technologist

Job Description

The Quality Control Technologist ensures that products consistently meet established quality, safety, and regulatory standards by performing laboratory testing, maintaining documentation, and supporting continuous improvement initiatives. This role involves working in a fast-paced laboratory environment, collaborating closely with the Quality Assurance team, and exercising Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) to maintain high levels of product compliance and operational excellence.

Responsibilities

• Review and maintain product compliance specifications and ensure all documentation remains accurate, current, and properly controlled.

• Gain proficiency in all assigned testing areas and perform laboratory tests according to established Standard Operating Procedures (SOPs).

• Document testing results clearly and accurately, including recording data, observations, and conclusions in accordance with GMP, GLP, and ISO requirements.

• Evaluate and determine the aesthetic quality of finished products, ensuring they meet defined visual and quality standards.

• Maintain consistency and accuracy in training tasks and records within Master Control or equivalent documentation systems.

• Maintain and adhere to SOP criteria for inspection and testing activities, ensuring consistent application of procedures.

• Exercise full compliance with GMP and GLP requirements in all aspects of the work environment and testing processes.

• Collaborate closely with the Quality Assurance department as part of a unified quality team to resolve issues and support quality initiatives.

• Participate in and support continuous improvement programs within the department, identifying opportunities to enhance processes and efficiency.

• Understand and follow all safety requirements and procedures, including proper handling of materials, equipment, and laboratory hazards.

• Assist in maintaining standards in accordance with GMPs, SOPs, and ISO regulations, contributing to regulatory and audit readiness.

Essential Skills

• Quality control or quality assurance experience in a laboratory setting, with a minimum combined 12 years of related QC/QA or microbiology laboratory work, or an equivalent combination of education and experience.

• Laboratory experience in a biological sciences laboratory, particularly in microbiology, is preferred.

• Familiarity with FDA regulations for medical devices or similar regulated products.

• Ability to manage multiple tasks in an organized fashion while meeting deadlines in a high-volume environment.

• Ability to adapt to and learn new procedures while maintaining a scientific and objective approach.

• Strong teamwork spirit with the ability to collaborate effectively across departments.

• Self-motivated and highly responsible approach to work, with strong attention to detail.

Additional Skills & Qualifications

• Experience working under GMP, GLP, and ISO-regulated environments.

• Exposure to medical device or related regulated industry environments.

• Demonstrated experience in documentation control and maintaining compliance records.

• Experience using Master Control or similar document management or quality management systems.

• Strong written and verbal communication skills to document results and collaborate with cross-functional teams.

• Proven ability to thrive in a fast-paced laboratory setting while maintaining accuracy and quality.

• Demonstrated commitment to continuous improvement and process optimization.

• Ability to maintain a scientific mindset and objective approach when troubleshooting and interpreting test results.

Job Type & Location

This is a Contract position based out of Lenexa, KS.

Pay and Benefits

The pay range for this position is $20.00 - $23.00/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 Lenexa,KS.

Application Deadline

This position is anticipated to close on Oct 23, 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 [e-mail] 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.