Quality Control Technologist

Oxoid Remel Microbiology; Lenexa (KS); On-site; USD 52,000 - 76,000; Full time

Job summary

Oxoid Remel Microbiology, now under Astorg ownership, seeks a Quality Control Technologist to ensure finished product testing aligns with IFU, SOPs, and regulatory standards. You will document results, maintain training, and support GMP/GDP compliance within a fast-paced lab.

The role emphasizes teamwork, accurate data handling, and adherence to safety protocols in a modern microbiology environment, with opportunities to contribute to product release activities and continuous improvement.

Qualifications

• Four-year degree in biological sciences with microbiology coursework and lab component.
• 1–2 years of QC/QA or microbiology lab experience or equivalent.
• Familiarity with FDA regulations for medical devices.
• Ability to manage multiple tasks in an organized manner.
• Strong written and verbal English communication; proficient with MS Office.
• Willingness to work weekends/overtime when needed.

Responsibilities

• Review and maintain product compliance specifications and documentation control.
• Perform and interpret microbiology testing, including growth promotion, biochemical testing, and AST.
• Gain proficiency on all performance benches.
• Document testing results and determine product disposition.
• Maintain training within Master Control and SOP criteria for inspection and testing.
• Maintain department equipment and request consumables as needed.
• Ensure GMP and GDP compliance in the work environment.
• Support continuous improvement initiatives within the department.

Skills

Teamwork

Verbal communication

Written communication

Critical thinking

Time management

Education

Bachelor's degree in biological sciences

Tools

Microsoft Word

Excel

PowerPoint

SAP

Job description

Summary Joining our team, you’ll play an active part in helping to deliver meaningful impact. At Oxoid Remel Microbiology, acquired from Thermo Fisher Scientific, we play a crucial role in accurate identification and targeted treatment for diseases, ensuring food and beverage safety, and supporting pharmaceutical manufacturing integrity. Our products and services are designed to meet the highest standards of quality and performance, helping our customers achieve their objectives efficiently and effectively.
Make a difference on a global scale. Our mission empowers customers to improve the world every day. Join our team and help solve tough challenges, such as environmental protection, food safety, and finding cures for cancer.

Position Summary The Quality Control Technologist will ensurethat performance of finished product is in compliance with testing standards per IFU and SOPs, in addition to customer requirements and regulatory agency guidelines.
Perform documentation control duties per Quality Assurance compliance requirements and is responsible for all quality control aspects of finished product testing.

Key Responsibilities

• Review and maintain product compliance specifications and documentation control.
• Perform and interpret microbiology testing, including growth promotion, biochemical testing, and AST.
• Gain proficiency on 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 needed.
• Exercise and monitor GMP and GDP compliance in the work environment.
• Execute Stability Study testing in accordance with QA requirements.
• Work in conjunction with Customer Service Representatives to achieve on-time product releases for standing orders and special products.
• Support continuous improvement initiatives within the department.
• Work closely with a team in a fast-paced laboratory setting.
• Understand and follow all safety requirements and procedures.
• Assist in maintaining standards in accordance with GMPs, SOPs, and ISO regulations.
• Train newly added team members.
• Participate in achieving department goals.
• Support all company policies.
• Perform other duties as assigned.

Minimum Requirements/Qualifications

• Possess at least a four-year degree in the biological sciences, including coursework in microbiology with a laboratory component, or an equivalent four-year degree.
• Have a minimum of 1-2 years of combined experience in QC/QA, microbiology laboratory work, or an equivalent combination of education and experience.
• Demonstrate familiarity with FDA regulations for medical devices.
• Possess the ability to manage multiple tasks in an organized manner.
• Have intermediate computer skills, preferably including Microsoft Word, Excel, and PowerPoint; SAP experience is a plus.
• Listen to and follow written and verbal instructions.
• Adapt to and learn new procedures while maintaining a scientific and objective approach.
• Be available to work weekend shifts and overtime when needed.
• Be self-motivated, highly responsible, and possess strong teamwork skills.
• Demonstrate excellent verbal and written communication skills in English.
• Must be willing to work overtime when needed to complete tasks.
• Must possess strong critical thinking skills.

This is an exciting time to join us as we continue to build on more than 100 years of microbiology excellence. With a broad portfolio of instruments, services, and global resources, we’re steadfast in our commitment to helping you succeed. Together, we can cultivate a thriving microbiology culture that supports you today, tomorrow, and for life. Oxoid Remel Microbiology, acquired from Thermo Fisher Scientific, is now under the ownership of Astorg, a leading private equity firm with deep healthcare sector expertise and proven track record in diagnostics. With the continuity of trusted brands, established expertise and a long-standing reputation in microbiology, we’re looking for talented people to join us as we enter our next chapter of growth. Come and be part of what’s next for our company.