Quality Control Analyst
Job in
Saint Paul, Ramsey County, Minnesota, 55199, USA
Listed on 2026-09-20
Listing for:
Spectraforce Technologies
Full Time
position Listed on 2026-09-20
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Job Description & How to Apply Below
Position Title: Quality Control Analyst
Work Location: St. Paul, MN (Onsite)
Assignment Duration: 12 Months
Work Schedule: Monday-Friday, 6:00 AM - 3:30 PM
Work Arrangement: Onsite
Position SummaryWe are seeking a detail-oriented Quality Control Analyst to perform biological, chemical, and physical testing of medical device products throughout various stages of the manufacturing process. This role analyzes raw materials, in-process samples, finished products, and environmental monitoring samples while ensuring compliance with FDA, GLP, QSR, and cGMP regulations.
Key Responsibilities- Perform laboratory testing on raw materials, in-process samples, finished products, and environmental monitoring samples.
- Conduct biological, chemical, and physical analyses using laboratory instrumentation and analytical equipment.
- Utilize laboratory computer systems, including LIMS, to accurately document and maintain test results.
- Execute analytical assays and testing protocols while ensuring data integrity and accuracy.
- Complete routine and special project testing within established timelines.
- Prepare and maintain laboratory documentation, including deviations, investigations, and exception reports.
- Ensure compliance with SOPs, FDA regulations, GLP, QSR, and cGMP requirements.
- Assist in laboratory audits, manufacturing audits, and continuous quality improvement initiatives.
- Review, update, and maintain standard operating procedures (SOPs).
- Perform equipment maintenance, calibration, and troubleshooting as needed.
- Collaborate with cross-functional teams to improve processes, efficiency, and product quality.
- Bachelor's Degree in Chemistry, Biochemistry, Biology, Microbiology, Biological Sciences, or a related Life Science discipline.
- 0-2 years of laboratory, quality control, analytical chemistry, microbiology, medical device, pharmaceutical, or biotech experience.
- Understanding of GMP/cGMP, GLP, FDA, and quality system regulations.
- Experience working with laboratory instrumentation and analytical testing methods.
- Familiarity with LIMS or other laboratory documentation systems is preferred.
- Strong documentation, data analysis, and problem-solving skills.
- Ability to manage multiple priorities in a fast-paced laboratory environment.
- Strong verbal and written communication skills.
- Proficiency with Microsoft Office and computer-based systems.
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