QA Technician

Position Overview:

• The Quality Technician is a hands-on role supporting the inspection, documentation, and quality assurance of medical devices during early-stage R&D builds.
• This position plays a critical role in ensuring product integrity and compliance by performing detailed inspections, maintaining accurate records, and collaborating with cross-functional teams to uphold quality standards throughout the development process.
• The ideal candidate is detail-oriented, methodical, and committed to maintaining high standards in a fast-paced, collaborative environment.
• Experience in regulated industries, especially medical devices, is highly valued.

Responsibilities:

• Conduct in-process and final inspections of small, intricate components and assemblies, validation of manufacturing equipment / processes, and setup of QA inspection and test processes.
• Review and interpret engineering drawings, specifications, and quality documentation to ensure compliance
• Record inspection results, deviations, and observations with precision and clarity
• Maintain accurate and organized documentation in accordance with GMP and ISO 13485 standards
• Collaborate with engineers to identify and resolve quality issues, and perform root cause analysis and investigation activities
• Assist in the documenting non-conformances and contributing to root cause analysis and corrective actions
• Ensure adherence to cleanroom protocols and quality control procedures during all build activities

Key Decision Rights:

• Escalate quality concerns, deviations, and non-conformances
• Provide input on inspection criteria, documentation practices, and process improvements

Required Skills and Competencies:

• Strong attention to detail and ability to perform precise inspections under magnification
• Familiarity with quality control principles and documentation practices in a regulated environment
• Ability to interpret technical drawings, specifications, and inspection criteria
• Ability to follow detailed instructions and maintain focus on repetitive tasks
• Strong communication skills and willingness to ask questions and learn
• Familiarity with basic computer tools for data entry and documentation
• Experience working in a regulated manufacturing or R&D environment preferred

Education and Experience:

• High School Diploma or equivalent required
• Minimum 3 years of experience in a quality, manufacturing, or assembly tech/operator role
• Experience in medical device or cleanroom environments is a plus

Additional Information:

• Role is based in Acton, MA and requires on-site presence 5 days per week.
• Cleanroom gowning and adherence to GMP/ISO standards may be required

Dexian stands at the forefront of Talent + Technology solutions with a presence spanning more than 70 locations worldwide and a team exceeding 10,000 professionals. As one of the largest technology and professional staffing companies and one of the largest minority-owned staffing companies in the United States, Dexian combines over 30 years of industry expertise with cutting-edge technologies to deliver comprehensive global services and support.


Dexian connects the right talent and the right technology with the right organizations to deliver trajectory-changing results that help everyone achieve their ambitions and goals. To learn more, please visit .


Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status.