Medical Device QA Technician: Precision Inspector

Signature Consultants; Massachusetts; On-site; USD 65,000 - 90,000; Full time

Job summary

Signature Consultants is seeking a Quality Technician to support inspection, documentation, and QA for early-stage medical device R&D builds in Acton, MA. The role requires meticulous inspection, accurate record-keeping, and collaboration with engineers to uphold GMP and ISO 13485 standards.

The ideal candidate has at least 3 years in a regulated manufacturing or R&D environment, familiar with cleanrooms and documentation practices.

Qualifications

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

Responsibilities

• Perform in-process and final inspections of small components and assemblies; validate manufacturing equipment/processes; set up 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; perform root cause analysis and investigation activities.
• Assist in 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.

Skills

Attention to detail

Inspect under magnification

Reading drawings

Quality documentation

Regulated environment

Communication

Data entry

Root cause analysis

Education

High School Diploma or equivalent

Job description

Signature Consultants is seeking a Quality Technician to support inspection, documentation, and QA for early-stage medical device R&D builds in Acton, MA. The role requires meticulous inspection, accurate record-keeping, and collaboration with engineers to uphold GMP and ISO 13485 standards.

The ideal candidate has at least 3 years in a regulated manufacturing or R&D environment, familiar with cleanrooms and documentation practices.