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Manufacturing Technician III

Job in Burlington, Middlesex County, Massachusetts, 01805, USA
Listing for: Glaukos
Full Time position
Listed on 2026-01-12
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Medical Device Industry, Manufacturing Production, Operations Engineer
Job Description & How to Apply Below

How will you make an impact?

You will be responsible for the following:
Perform kitting operations (measure out components or raw materials) Ability to perform activities under a microscope Prepare components and build device assemblies Prepare bulk drug formulations Perform filing, capping, and crimping operations Perform packaging and labeling operations Perform sampling Perform visual inspections Perform documentation and data input into materials requirement planning (MRP), Batch Records (BRs), and Device History Record (DHR) Perform all activities with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality management system (QMS) medical device good manufacturing practices (GMP) requirements.

Additional tasks as required

How will you get here?
  • High School Diploma Required
  • 4-6 years of related experience in the medical device, pharmaceutical, and/or biotechnology industries, or a AA with less 2-4 years of experience or a bachelor’s degree with 0-2 years of experience. Required
  • It is highly desirable to have experience working in and maintaining a cleanroom in accordance with GDP and cGMPs standards. Required
What will you do?
  • Maintain proper cleanroom environment (including gowning, room cleaning, and supplies)
  • 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 calculation and data entry
  • Ability to assemble, disassemble, and clean process equipment
  • Ability to clean, etch, passivate, assemble, and inspect components
  • Process and assemble components in accordance with documented specifications and procedures
  • Prepare bulk drug formulation operations
  • Perform filling, capping and crimping operations
  • Perform packaging and labeling operations
  • Perform in-process inspection of assemblies and finished products in accordance with specification criteria
  • Organize and clean the work areas
  • Ability to perform validation and qualification activities (IQ/OQ/PQ/PV)
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