QC Microbiology Lab Technician (GMP/GLP)

Actalent; Olathe (KS); On-site; USD 28,000 - 32,000; Part time

Benefits offered by this job

Medical, dental & vision

401(k) retirement plan

Life Insurance

Disability insurance

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

PTO

Job summary

Actalent is seeking a meticulous QC Tech III in Lenexa, KS to ensure product compliance and maintain documentation control. You will gain proficiency in testing areas, document results, and determine the aesthetic quality of finished products.

This role supports Master Control training tasks and SOP criteria for inspection and testing. The position operates Monday to Friday, 8:00 AM to 5:30 PM onsite with a focus on GMP/GLP compliance, equipment upkeep, and continuous improvement within the

Qualifications

• Quality control and microbiology expertise.
• Minimum of 1-2 years of experience in related QC/QA, microbiology laboratory work, or an equivalent combination of education and experience.
• Familiarity with FDA regulations for medical devices.
• Ability to manage tasks in an organized manner.
• Intermediate computer skills, with proficiency in Microsoft Word, Excel, and PowerPoint, as well as SAP.

Responsibilities

• Maintain and review product compliance specifications and documentation.
• Gain proficiency in all testing areas and document testing results.
• Determine aesthetic quality on finished products.
• Ensure SOP criteria for inspection and testing are met.
• Responsible for maintaining department equipment and ordering consumable stock supplies when necessary.
• Exercise GMP and GLP compliance in the work environment.
• Contribute to the continuous improvement program within the department.
• Assist in maintaining standards in accordance with GMP's/SOP's and ISO regulations.

Skills

Quality control

Microbiology

QC experience

FDA regulations

Tools

SAP

Microsoft Office

Job description

Actalent is seeking a meticulous QC Tech III in Lenexa, KS to ensure product compliance and maintain documentation control. You will gain proficiency in testing areas, document results, and determine the aesthetic quality of finished products.

This role supports Master Control training tasks and SOP criteria for inspection and testing. The position operates Monday to Friday, 8:00 AM to 5:30 PM onsite with a focus on GMP/GLP compliance, equipment upkeep, and continuous improvement within the