Job summary
Job post source
This job is directly from Cytek Biosciences
Job overview
The QC Inspector role at Cytek Biosciences ensures the quality of IVD manufacturing components and products, directly impacting patient safety and regulatory compliance.
Responsibilities and impact
The QC Inspector uses precision measurement tools to verify materials and products, analyzes discrepancies, manages quality reports, supports complaint investigations, and collaborates with cross-functional teams to drive continuous improvement and uphold ISO 13485 and GMP standards.
Experience and skills
Candidates need a high school diploma or GED, with a BS in Engineering preferred, and skills in dimensional tools, GD&T, root-cause analysis, and reading engineering documentation; certifications like CSQT or ASQ are a plus.
Career development
The role offers opportunities to advance in Quality Engineering, NPI, Calibration, or Quality Engineering pathways, with chances to pursue advanced certifications and develop expertise in Lean/Six Sigma and CMM programming.
Work environment and culture
Cytek Biosciences values transparent communication, lean-driven improvements, and a collaborative environment that celebrates success and quality focus.
Company information
Cytek Biosciences is an IVD diagnostics company focused on manufacturing high-quality instruments and kits, emphasizing patient safety and regulatory readiness.
Team overview
The QC Inspector works closely with Quality Engineers, Manufacturing, NPI, and R&D teams to ensure product quality and process improvements.
Application process
Applicants are encouraged to apply by describing their experience with defect identification, process improvements, and inspection tools, highlighting problem-solving approaches.
Unique job features
The job features hands-on use of advanced measurement tools, involvement in Lean/Six Sigma initiatives, and a direct impact on patient safety and product quality.
Company overview
Cytek Biosciences, Inc. is a biotechnology company specializing in flow cytometry, providing advanced cell analysis solutions. They generate revenue through the sale of their proprietary instruments, reagents, and software, which are used in research and clinical diagnostics. Founded in 2014, Cytek has made significant strides in the field by developing innovative technologies such as the Full Spectrum Flow Cytometry (FSFC) platform. This platform allows for more comprehensive and accurate cell analysis, setting Cytek apart in the competitive biotech landscape.
How to land this job
Position your resume to highlight your expertise with dimensional tools such as calipers, CMMs, and micro-VUs, emphasizing your ability to perform precise inspections in a regulated manufacturing environment.
Emphasize experience with root-cause analysis, statistical reporting, and familiarity with quality systems like ISO 13485 and GMP, as well as your skills in collaborating cross-functionally with engineering, manufacturing, and suppliers.
Apply through multiple platforms including Cytek Biosciences' official career page, LinkedIn, and relevant job boards to maximize your application visibility for the QC Inspector role.
Connect on LinkedIn with quality engineers, manufacturing leads, or NPI team members at Cytek Biosciences; open conversations by referencing recent product launches, expressing curiosity about their quality improvement initiatives, or asking about their experience with Lean/Six Sigma practices.
Optimize your resume for ATS by incorporating keywords such as 'CMM programming,' 'Lean/Six Sigma,' 'root-cause analysis,' 'ISO 13485,' 'GMP,' 'MRP,' and 'DHR' to ensure your resume passes initial automated screenings.
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