R&D Medical Device Assembly Technician (On-Site, Acton)

Proclinical; Acton (MA); On-site; USD 30,000 - 47,000; Full time

Job summary

Proclinical is seeking a R&D Assembly Technician in Acton, MA for a contract role supporting the development and assembly of medical devices in a cleanroom environment. You will work with manual and semi-automated equipment, following detailed work instructions, and documenting observations and outcomes to support engineering analysis.

On-site 5 days per week from 8am to 5pm, familiarity with GMP/ISO standards is preferred, and strong attention to detail plus a collaborative approach will help

Qualifications

• High School Diploma or equivalent.
• Minimum 3 years of experience in manufacturing, R&D, or assembly tech/operator role.
• Experience in medical devices or cleanroom environments is a plus.

Responsibilities

• Perform manual and semi-automated assembly of small, intricate components for early-stage R&D builds.
• Operate and maintain basic manufacturing and inspection equipment in a cleanroom or lab environment.
• Follow detailed work instructions, assembly drawings, and process documentation.
• Record observations, process data, and build outcomes to support engineering analysis.
• Collaborate with engineers to share feedback, suggest improvements, and support process refinement.
• Assist in setup and troubleshooting of assembly fixtures and semi-automated tools.
• Support documentation of learnings, deviations, and process updates as needed.

Skills

Attention to detail

Microscope work

Follow detailed instructions

Communication skills

Documentation

Regulated environment awareness

Education

High School Diploma or equivalent

3 years manufacturing/R&D/assembly experience

Tools

Documentation tools

Job description

Proclinical is seeking a R&D Assembly Technician in Acton, MA for a contract role supporting the development and assembly of medical devices in a cleanroom environment. You will work with manual and semi-automated equipment, following detailed work instructions, and documenting observations and outcomes to support engineering analysis.

On-site 5 days per week from 8am to 5pm, familiarity with GMP/ISO standards is preferred, and strong attention to detail plus a collaborative approach will help