QC Inspector II (1st Shift)

TransMedics•Andover, MA

1d•Onsite

About The Position

Performs inspection of critical components and completed assemblies used in Class III medical devices. Conducts visual and dimensional inspection of sub-assemblies or final system assemblies, during or post manufacturing processes. Interprets manufacturing procedures, drawings, and assembly inspection instructions in approving or rejecting in-process or final assemblies. This role is for a first shift position, with standard working hours from 6am to 2:30pm.

Requirements

1-3 years of Quality Control Experience in Medical Device Manufacturing.
High School Diploma or equivalent job experience with additional training in the trade; or equivalent combination of education and experience
Understanding of CGMP and GDP required
Intermediate computer knowledge required.
Working knowledge of Microsoft Word, and Outlook required.
Must be proficient in written and spoken English.
Ability to read, interpret, and understand drawings, blueprints, and specifications.
Must possess intermediate math skills: addition, subtraction, multiplication, division, and efficient use of a calculator.
Knowledge of inspection tools such as rulers and vernier calipers required.

Nice To Haves

Prior experience working in clean room environments.
Excellent verbal and written communication skills.
Strong math skills including measuring dimensions using calibrated tools, and calculating specifications.
Knowledge of Microsoft Excel, Access, Powerpoint a plus.
Ability to work overtime hours, or support weekend operations a plus.
Other visual/cosmetic inspection tools such as Tappi Charts a plus.

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 (equipment, associate, and material).
Identifies and documents non-conformances to specifications.
Conducts batch record review and release, including review of NCMR’s, deviations etc.
Perform other TransMedics tasks and duties as assigned/required.