Medical Device QC Inspector II - Visual & Dimensional

TransMedics, Inc.; Andover (MA); On-site; USD 34,040 - 48,450; Full time

Benefits offered by this job

Medical with HRA

401K Plan

Employee Stock Purchase Plan

Job summary

TransMedics, Inc. is seeking a Quality Inspector to perform visual and dimensional inspection of components and assemblies in a Class III medical device environment.

The role involves interpreting procedures and drawings to approve or reject in-process and final products, with a first shift from 6am to 2:30pm. The ideal candidate has 1–3 years of QC experience in medical device manufacturing, understands CGMP/GDP, and can read blueprints.

Qualifications

• 1-3 years of Quality Control Experience in Medical Device Manufacturing.
• High School Diploma or equivalent plus additional training in the trade; or equivalent combination of education and experience.
• Understanding of CGMP and GDP required.
• Intermediate computer knowledge; Microsoft Word and Outlook proficiency.

Responsibilities

• Performs intermediate visual and dimensional inspection of product at in-process assembly and/or final inspection.
• Approves finished products by confirming specifications, conducting visual and measurement tests, returning products for re-work.
• Reviews products for re-work and confirms conformity to required quality specifications.
• Ensures departmental compliance to all company policies relative to the manufacture of product, lot control requirements, documentation requirements, and safety.
• Identifies and documents non-conformances to specifications.
• Conducts batch record review and release, including review of NCMRs, deviations etc.

Skills

English proficiency

Reading blueprints

Math skills

Inspection tools

Education

High School Diploma or equivalent

Tools

Microsoft Word

Outlook

Job description

TransMedics, Inc. is seeking a Quality Inspector to perform visual and dimensional inspection of components and assemblies in a Class III medical device environment.

The role involves interpreting procedures and drawings to approve or reject in-process and final products, with a first shift from 6am to 2:30pm. The ideal candidate has 1–3 years of QC experience in medical device manufacturing, understands CGMP/GDP, and can read blueprints.