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Microbiology Lab Technician
Career Insights for Quality Control Analyst
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Based on Kentucky data
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What they do
A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.
$53,614 / year median in Kentucky
-16% projected decline
Job Description
- Perform routine microbiological testing on raw materials and finished products
- Support administration of the environmental monitoring program
- Participate in investigations related to microbial data deviations
- Troubleshoot laboratory equipment and testing methods
- Support equipment validation, qualification, calibration, and preventive maintenance activities
- Maintain laboratory records, data archives, and sample inventories
- Document laboratory activities in compliance with GLP/cGMP requirements
- Manage and document changes through quality systems and change control processes
- Compile and trend microbiological data
- Support quality audits and quality management system activities
- Assist with stability studies and product performance evaluations
- Order laboratory supplies and chemicals as needed
- Maintain laboratory cleanliness, safety, and compliance standards
- Identify and address potential safety and quality risks Follow all company safety procedures and regulatory requirements We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day.
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https://insightglobal.com/workforce-privacy-policy/. Skills and Requirements Must-Haves- Bachelor's degree in Microbiology, Biology, Chemistry, or related scientific field (or equivalent laboratory experience)
- 1+ year of microbiology, quality control, quality assurance, or laboratory experience
- Strong understanding of quality control processes and laboratory best practices
- Experience with aseptic technique and laboratory documentation
- Familiarity with GLP and/or cGMP requirements
- Experience following SOPs and maintaining accurate records
- Strong communication and collaboration skills Ability to work in a fast-paced laboratory environment Plusses
- ISO-regulated environment experience
- Experience supporting environmental monitoring programs
- Experience with equipment validation, qualification, calibration, and preventive maintenance
- Experience with CAPA, change control, document control, or quality management systems Previous experience supporting quality audits or investigations involving microbial deviations