Demo

Quality Control Technician

Bolt Medical
Carlsbad, CA Full Time
POSTED ON 1/21/2025
AVAILABLE BEFORE 4/20/2025

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES.

RECRUITERS : DO NOT CONTACT.

Role Description

The Quality Inspector performs incoming inspection, in-process inspections, and final inspections of components and assemblies per control / quality plans. The Quality Inspector will review and approve final release documentation. Performs incoming inspections per control / quality plans for received materials. This role will also complete appropriate quality records within company and GMP guidelines, policies and procedures.

Roles and Responsibilities

  • Inspect incoming or production materials for conformance to engineering drawings, schematics, and specifications; process standards and specifications; and production or process plans.
  • Perform incoming test of components. Monitor for conformance to design or test specifications or standards.
  • Accept or reject materials or articles; identify and document non-conformance and notify appropriate personnel of potential rejection of items.
  • Refer / document unusual inspection problems to supervision, lead or Project Quality Engineer.
  • Know using a variety of measuring tools including electrical test sets, multimeter, fixed, limit, plug-gages, steel rules, scales, micrometers, calipers, and surface plate.
  • Assist in the writing and updating of inspection procedures, protocol, and checklists.
  • Transferring, releasing or quarantining material physically according to inspection status
  • Documenting and maintaining inspection and test records
  • Understand the importance of product conformity.
  • Understand lot numbers and traceability.
  • Understand ISO 13485 quality assurance standards and the related documentation in support of.
  • Maintains safe and clean work environment by keeping shelves, workstations, etc. neat and complying with procedures, rules and regulations.
  • Complete respective paperwork / documentation.

Education :

  • Minimum of High School Diploma and two years or more working experience in a relevant, cGMP / FDA regulated industry.
  • Required Knowledge & Experience :

  • Be able to read and understand mechanical drawings and dimensions
  • Be able to read and interpret drawing notes and able to understand configuration management (revision control)
  • Be able to use basic measuring tools such as calipers, go-no / go gauges, torque wrenches, and others as necessary
  • Experience with electrical test sets, multimeter, vision measuring system is a plus
  • Experience working with an ERP system and data entry
  • Experience with Outlook and MS Office.
  • Good communication and organizational skills.
  • Must possess good math fundamentals, comprehend written work instructions, and communicate well.
  • Knowledge of medical device manufacturing
  • Working understanding of GDP and GMP
  • Excellent documentation skills, attention to detail and accuracy
  • Team player, flexible multitask, good written / oral communicator
  • Must be organized and able to coordinate activities with internal departments and outside vendors
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