Job Description
Job DescriptionQuality Control - Microbiologist
Job Description
As a Microbiologist, you will be part of a dedicated Quality Control team responsible for ensuring that all finished product testing meets the highest standards of compliance. You will work closely with the Quality Assurance department and other teams to ensure product quality and compliance with customer requirements and regulatory guidelines.
Responsibilities
- Oversee all quality control aspects of finished product testing.
- Ensure product performance compliance with testing standards, IFU, SOPs, and regulatory guidelines.
- Manage documentation control duties as per Quality Assurance compliance requirements.
- Review, maintain, and interpret microbiology testing results, including growth promotion, biochemical, and AST.
- Gain proficiency in all performance benches.
- Document testing results and 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 necessary.
- Exercise and monitor GMP compliance within the work environment.
- Collaborate with the Quality Assurance department as part of a quality team.
- Execute Stability Study testing in accordance with QA requirements.
- Work alongside Customer Service Representatives to ensure timely product releases.
- Participate in continuous improvement programs within the department.
- Work in a fast-paced laboratory setting.
- Understand and adhere to all safety requirements and procedures.
- Assist in maintaining standards according to GMPs, SOPs, and ISO regulations.
- Support all company policies and participate in achieving department goals.
- Perform other duties as assigned.
Essential Skills
- 4-year degree in biological sciences with coursework in microbiology
- 1-2 years of experience in related QC/QA, microbiology laboratory work, or equivalent combination of education and experience.
- Familiarity with FDA regulations for medical devices.
- Intermediate computer skills, particularly in Microsoft Word, Excel, and PowerPoint.
- Experience with SAP is a plus.
- Ability to manage tasks efficiently and in an organized manner.
- Effective communication skills with various departments regarding quality testing.
- Ability to learn new procedures and maintain a scientific and objective approach.
- Availability to work weekend shifts when needed.
- Self-motivated, highly responsible, and a good team player.
- Excellent verbal and written skills in English.
Work Environment
This position is based in a laboratory environment, with standard working hours from Monday to Friday, 8 AM to 5 PM. The role may require weekend shifts and overtime as needed. It is a long-term contract opportunity within a pharmaceutical/medical device facility.
Pay and Benefits
The pay range for this position is $23.00 - $25.00/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 Oct 15, 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.