Precision Medical Device Assembler & QA Technician

Groe Advisors LLC

Burlington (MA)

On-site

USD 52,000 - 78,000

Full time

3 days ago
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Job summary

Groe Advisors LLC in Burlington, MA is seeking a detail-oriented assembler for medical device manufacturing. You will perform kitting, assemble and test devices, and maintain strict GDP/cGMP documentation.

The role requires hands-on skills with tools, microscope work, and precise data entry into BRs, DHRs, and MRP systems; you will ensure quality through in-process inspection and validation activities.

Qualifications

  • Experience performing kitting and component preparation
  • Familiar with cGMP, GDP, and QA documentation
  • Ability to document data into BRs, DHRs, and MRP systems
  • 2–4 years in medical devices assembly

Responsibilities

  • Follow, execute, and adhere to documentation in accordance with cGMP, QMS, and GDP requirements: protocols, specifications, work instructions (WIs), standard operating procedures (SOPs), batch records (BRs), device history records (DHRs), and engineering batches.
  • Perform basic calculations and data entry
  • Ability to assemble, disassemble, and clean process equipment
  • Process and assemble components in accordance with documented specifications and procedures
  • Perform mechanical, optical, and system assembly, and conduct thorough testing
  • Perform packaging and labeling operations
  • Perform in-process inspection of assemblies and finished products in accordance with specification criteria
  • Perform treatment card programming
  • Organize and clean the work areas
  • Ability to perform validation and qualification activities (IQ/OQ/PQ/PV)

Skills

Hand tools proficiency
Precision measurement
Documentation
GDP / cGMP knowledge
Data entry

Tools

Microscope
Measuring instruments
Process equipment

Job description

Groe Advisors LLC in Burlington, MA is seeking a detail-oriented assembler for medical device manufacturing. You will perform kitting, assemble and test devices, and maintain strict GDP/cGMP documentation.

The role requires hands-on skills with tools, microscope work, and precise data entry into BRs, DHRs, and MRP systems; you will ensure quality through in-process inspection and validation activities.

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