Quality Control Technician

Clarapath; New York, Northern (NY, KY); Hybrid; USD 55,000 - 85,000; Full time

Benefits offered by this job

Competitive salary

Benefits package

Collaborative environment

IP filing opportunities

Research collaborations

Strategic leadership collaboration

Mission driven organization

Job summary

Clarapath in Westchester County, NY, is seeking a Quality Control Technician to ensure the quality and reliability of our SectionStar and TrimStar Pro platforms. You will perform incoming, in-process, and final inspections, document results, and participate in nonconformance investigations.

Join a fast-paced manufacturing environment that collaborates with engineering, software, and manufacturing teams to maintain high standards, meet specifications, and support continuous improvement

Qualifications

• High school diploma or equivalent; technical degree or certification in manufacturing, engineering technology, quality, or a related field, is a plus.
• 1-3 years of experience in quality control, manufacturing, inspection, or a related technical environment preferred.
• Experience reading engineering drawings, specifications, and work instructions.
• Experience using precision measurement tools such as calipers, micrometers, gauges, and similar inspection equipment.
• Strong attention to detail and ability to identify discrepancies or defects.
• Familiarity with ISO 13485 or other regulated quality systems is a plus.
• Familiarity with nonconformance, CAPA, and root cause analysis is a plus.

Responsibilities

• Perform incoming, in-process, and final inspections of components, assemblies, and finished products
• Inspect parts and assemblies against engineering drawings, specifications, work instructions, and established quality standards
• Use precision measurement equipment such as calipers, micrometers, gauges, and other inspection tools
• Perform functional and quality testing of mechanical, electrical, and electromechanical assemblies
• Document inspection and test results accurately and maintain required quality records
• Identify, document, and communicate nonconforming materials, components, and assemblies
• Support nonconformance investigations and assist with root cause analysis and corrective actions
• Work closely with Manufacturing and Engineering to resolve quality issues and prevent recurrence
• Assist with first article inspections and inspection activities associated with new or modified products
• Verify that manufacturing processes are being performed in accordance with approved procedures and work instructions
• Support calibration and maintenance of inspection and measurement equipment
• Assist with maintaining inspection procedures, checklists, and other quality documentation
• Review manufacturing documentation for completeness and accuracy
• Participate in continuous improvement initiatives focused on product quality, process consistency, and manufacturing efficiency
• Maintain a clean, organized, and safe inspection and work environment
• Support quality activities associated with product builds, engineering verification, and production releases
• Assist with audits and other Quality Management System activities as needed

Skills

Reading engineering drawings

Attention to detail

Documentation

Analytical thinking

Cross-functional collaboration

Education

High school diploma or equivalent

Technical degree or certification in manufacturing/engineering technology/quality

Tools

Calipers

Micrometers

Gauges

Job description

Clarapath is a medical robotics company based in Westchester County, NY, dedicated to transforming and modernizing laboratory workflows. Our mission is to improve patient care by increasing efficiency, reducing costs, and enhancing the quality and consistency of laboratory processes.

Our portfolio includes SectionStar™ and TrimStar Pro™, innovative electro-mechanical systems designed to automate and elevate critical steps in the histology workflow. SectionStar™ delivers high-quality, consistent tissue sections, while TrimStar Pro™ streamlines and standardizes the trimming process - together enabling laboratories to operate with greater precision, throughput, and reliability.

At Clarapath, we bring together experts across engineering, data science, robotics, healthcare innovation, and laboratory operations. Our R&D team drives innovation, product enhancements, and a strong pipeline of new solutions, while our manufacturing team oversees production and quality control at our ISO-certified facility. Also based in our New York headquarters are our sales, marketing, administrative, and service teams, who work closely together to ensure every customer receives a seamless, personalized experience at every touchpoint.

Role Summary

The Quality Control Technician will play a key role in ensuring the quality, reliability, and consistency of Clarapath's advanced SectionStar™ and TrimStar Pro™ platforms. This individual will support quality control activities throughout the product lifecycle, including incoming inspection, in-process and final inspection, testing, documentation, and identification of nonconformances. Working closely with manufacturing, mechanical, electrical, software, engineering, and quality teams, the Quality Control Technician will help ensure products and components meet established specifications, drawings, procedures, and quality standards. We are seeking a hands-on, detail-oriented individual who enjoys working in a fast-paced manufacturing environment, takes pride in maintaining high standards of quality, and is passionate about supporting the development of innovative medical device and robotics technologies that improve laboratory workflows and patient outcomes.

Responsibilities

• Perform incoming, in-process, and final inspections of components, assemblies, and finished products
• Inspect parts and assemblies against engineering drawings, specifications, work instructions, and established quality standards
• Use precision measurement equipment such as calipers, micrometers, gauges, and other inspection tools
• Perform functional and quality testing of mechanical, electrical, and electromechanical assemblies
• Document inspection and test results accurately and maintain required quality records
• Identify, document, and communicate nonconforming materials, components, and assemblies
• Support nonconformance investigations and assist with root cause analysis and corrective actions
• Work closely with Manufacturing and Engineering to resolve quality issues and prevent recurrence
• Assist with first article inspections and inspection activities associated with new or modified products
• Verify that manufacturing processes are being performed in accordance with approved procedures and work instructions
• Support calibration and maintenance of inspection and measurement equipment
• Assist with maintaining inspection procedures, checklists, and other quality documentation
• Review manufacturing documentation for completeness and accuracy
• Participate in continuous improvement initiatives focused on product quality, process consistency, and manufacturing efficiency
• Maintain a clean, organized, and safe inspection and work environment
• Support quality activities associated with product builds, engineering verification, and production releases
• Assist with audits and other Quality Management System activities as needed

Qualifications

• High school diploma or equivalent required; technical degree or certification in manufacturing, engineering technology, quality, or a related field, a plus
• 1-3 years of experience in quality control, manufacturing, inspection, or a related technical environment preferred
• Experience working with mechanical, electrical, or electromechanical products preferred
• Ability to read and interpret engineering drawings, specifications, and work instructions
• Experience using precision measurement tools such as calipers, micrometers, gauges, and similar inspection equipment
• Strong attention to detail and ability to identify discrepancies or defects
• Basic understanding of manufacturing and quality control principles
• Basic computer proficiency, including Microsoft Office or similar tools
• Strong organizational and documentation skills
• Ability to accurately record inspection and test results
• Strong analytical and problem-solving skills
• Ability to work effectively with Engineering, Manufacturing, and Quality teams
• Comfortable working in a hands-on manufacturing and laboratory environment
• Familiarity with ISO 13485 or other regulated quality systems, a plus.
• Experience in medical device, aerospace, robotics, or other regulated manufacturing environments, a plus.
• Familiarity with nonconformance, CAPA, root cause analysis, or corrective action processes, a plus
• Experience with inspection documentation or quality management systems, a plus

Company Offers

• Competitive salary will be commensurate with experience and education
• Comprehensive benefits package available: (healthcare, vision, dental and life insurances; 401k; PTO and holidays).
• A collaborative and diverse work environment where our teams thrive on solving complex challenges
• Ability to file IP with the company
• Connections with world class researchers and their laboratories
• Collaboration with strategic leaders in healthcare and pharmaceutical world
• A mission driven organization where every team member will be responsible for changing the standards of delivering healthcare

Clarapath is proud to be an equal opportunity employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. In addition to federal law requirements, Clarapath complies with applicable state and local laws governing nondiscrimination in employment. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.