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Job Title: QC Scientist IJob Description

As a Quality Control Technologist, you will be responsible for ensuring that all aspects of finished product testing meet the necessary quality standards. This role requires a proactive approach to maintaining compliance with testing standards, customer requirements, and regulatory guidelines. You will also be responsible for documentation control duties as per quality assurance compliance requirements.

Responsibilities

+ Review and maintain product compliance specifications and documentation control.

+ Perform and interpret microbiology testing, including growth promotion, biochemical tests, and antimicrobial susceptibility testing (AST).

+ Gain proficiency on all performance benches and document testing results to determine product disposition.

+ Maintain consistency in training within Master Control.

+ Establish and maintain SOP criteria for inspection and testing.

+ Maintain department equipment and request consumables as needed.

+ Ensure and monitor GMP compliance within the work environment.

+ Collaborate closely with the Quality Assurance department as part of the quality team.

+ Execute stability study testing in accordance with QA requirements.

+ Work with Customer Service Representatives to achieve on-time product releases for standing orders and special products.

+ Contribute to the continuous improvement program within the department.

+ Work collaboratively in a fast-paced laboratory setting.

+ Understand and adhere to all safety requirements and procedures.

+ Assist in maintaining standards in accordance with GMPs, SOPs, and ISO regulations.

+ Participate in achieving department goals and support all company policies.

+ Perform other duties as assigned.

Essential Skills

+ Possess at least a 4-year degree in biological sciences with coursework in microbiology, or a 4-year degree with 5+ years of microbiology lab experience.

+ At least 1-2 years of experience in related QC/QA or microbiology laboratory work, or an equivalent combination of education and experience.

+ Familiarity with FDA regulations for medical devices.

+ Ability to manage multiple tasks in an organized manner.

+ Effective communication skills with various departments regarding quality testing parameters.

+ Intermediate computer skills, particularly in Microsoft Word, Excel, and PowerPoint. Experience with SAP is a plus.

+ Ability to listen to and follow written and verbal instructions.

+ Adaptability to learn new procedures and maintain a scientific and objective approach.

+ Availability to work weekend shifts when needed.

+ Self-motivated, highly responsible, and possess a good teamwork spirit.

+ Excellent verbal and written skills in English.

Additional Skills & Qualifications

+ Experience in quality control and microbiology.

+ Good entry-level job for those starting in the field.

Work Environment

The position is located in Lenexa, Kansas, with work hours from Monday to Thursday or Tuesday to Friday, 7:00 AM to 05:30 PM. The role is set in a fast-paced laboratory environment where adherence to GMPs, SOPs, and ISO regulations is essential. The position requires a scientific approach and collaboration with various departments.

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 Nov 12, 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 [email protected] (%[email protected]) for other accommodation options.