Medical Device QC Inspector II - Precision & Compliance

Transmedics

Andover (MA)

On-site

USD 34,000 - 48,000

Full time

14 days+
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Benefits offered by this job

Medical with HRA
Dental
Vision Healthcare
401K Plan
Paid time off
Wellness resources
Employee Stock Purchase Plan

Job summary

TransMedics in Andover, MA is seeking a detail-oriented Quality Control Inspector to visually and dimensionally inspect components and assemblies used in Class III medical devices. You will approve finished products, review for re-work, and ensure conformance to specifications in a GMP environment.

The role requires 1–3 years of QC experience, familiarity with drawings and blueprints, and proficiency with inspection tools.

Qualifications

  • 1-3 years of quality control experience in medical device manufacturing.
  • High School Diploma or equivalent with additional training in the trade.
  • Understanding of CGMP and GDP.
  • Intermediate computer knowledge; MS Word/Outlook proficiency.
  • Ability to read, interpret, and understand drawings/blueprints.
  • Intermediate math skills: basic operations with calculator.

Responsibilities

  • Inspect components and assemblies visually and dimensionally.
  • Approve finished products by testing and confirming specifications.
  • Review products for re-work and ensure conformity to specs.
  • Ensure compliance with company policies, lot control, documentation, and safety.
  • Identify and document non-conformances to specifications.
  • Perform batch record review and release, including NCMR/deviations.
  • Perform other TransMedics tasks as assigned.

Skills

Quality control
Reading drawings
Math skills
English proficiency
Attention to detail

Education

High School Diploma or equivalent
Trade training or equivalent experience

Tools

Vernier calipers
Rulers
Tappi Charts

Job description

TransMedics in Andover, MA is seeking a detail-oriented Quality Control Inspector to visually and dimensionally inspect components and assemblies used in Class III medical devices. You will approve finished products, review for re-work, and ensure conformance to specifications in a GMP environment.

The role requires 1–3 years of QC experience, familiarity with drawings and blueprints, and proficiency with inspection tools.

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