Label Printing & Quality Control Specialist

AWT Labels & Packaging

Hauppauge (NY)

On-site

USD 25,000 - 33,000

Full time

25 hours ago
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Benefits offered by this job

Medical insurance
HSA
401k with match
Paid time off

Job summary

AWT Labels & Packaging is seeking a Label Control Operator for our Hauppauge, NY location. You will print onto clinical labels using scanning software and ensure output meets strict quality standards.

The role requires a high school diploma (college preferred), basic MS Excel/Word skills, and good English communication. Overtime hours may be required; strong attention to detail and GMP integrity are essential.

Qualifications

  • High School diploma required; college degree a plus.
  • cGMP/quality experience preferred.
  • Good working knowledge of MS Excel, Word and PC skills.
  • Ability to work flexible hours including overtime.
  • Must communicate well in English, both verbally and in writing.
  • Mechanical aptitude to operate office equipment.
  • Good eyesight, hearing, and depth perception.

Responsibilities

  • Operate label printers, scanners and inline inspection equipment.
  • Ensure GDP and cGMP paperwork is completed accurately.
  • Review print outputs for quality and specification conformance.
  • Manage and organize electronic files and file naming.
  • Change heat-transfer ribbons per job specifications.
  • Maintain clean work area and prevent cross-contamination.
  • Respond to management instructions and complete tasks efficiently.

Skills

Excel
Word
PC skills
Detail-oriented
Math
English proficiency

Education

High School Diploma
College degree a plus

Tools

Label printers
Scanners
Inline inspection equipment

Job description

AWT Labels & Packaging is seeking a Label Control Operator for our Hauppauge, NY location. You will print onto clinical labels using scanning software and ensure output meets strict quality standards.

The role requires a high school diploma (college preferred), basic MS Excel/Word skills, and good English communication. Overtime hours may be required; strong attention to detail and GMP integrity are essential.

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