Manufacturing Assembler

Delcath Systems Inc•Town of Queensbury, NY
•$17 - $19•Onsite

About The Position

We’re looking for a motivated and collaborative Manufacturing Assembler to join our growing team at Delcath. In this role, you’ll have the opportunity to make a meaningful impact while working alongside talented colleagues in a supportive and innovative environment. We're excited to provide a complete benefits package, including a comprehensive health plan, 401(k), and professional development opportunities, to support the well-being and growth of our employees and their families. The Manufacturing Assembler I will assist in the manufacture of disposable medical devices by fabricating, assembling, inspecting, labeling and packaging various medical device components. The incumbent will work the Manufacturing Engineer in general technician duties. These additional duties may include, but are not limited to performing basic metrology measurements and inspections, tensile testing, and leak testing.

Requirements

  • High School Diploma or equivalent with additional relevant training desired
  • 1-3 years’ experience in a manufacturing environment, preferably in the medical device industry
  • Ability to read, comprehend and follow written procedures and directions
  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
  • Ability to write routine reports and correspondence.
  • Ability to speak effectively with employees and outside organization
  • Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
  • Ability to compute rate, ratio, and percent and create and/or interpret spreadsheets and graphs.

Responsibilities

  • Fabricate, assemble, inspect, label & package medical device components and products to consistently high quality standards as directed
  • Strictly follow written procedures and maintain product and lot identification in accordance with company policies and good manufacturing practices
  • Timely notify the supervisor when documentation or procedural errors are noticed and provide recommendations for continuous improvement to comply with FDA and other regulatory requirements
  • Maintain accurate records for work performed
  • Understand and utilize measurement instruments to verify work quality
  • Perform project work, as assigned, for the Research and Development and Operations Departments
  • Contribute to and maintain a professional and respectful work environment

Benefits

  • comprehensive health plan
  • 401(k)
  • professional development opportunities
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