2nd Shift Manufacturing Technician — FastPack Kit Assembly

Qualigen Diagnostics, Inc.

Carlsbad (CA)

On-site

USD 25,000 - 36,000

Part time

13 days ago

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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
Life insurance
Retirement plan
Paid time off

Job summary

Qualigen Diagnostics, Inc. in Carlsbad, CA seeks a Manufacturing Technician for a 2nd shift temporary role to produce FastPack test kits. You will operate filling and sealing machines, label vials, and assemble kits according to FDA-compliant instructions.

Requirements include a high school diploma or equivalent, basic math, neat records, and clear spoken and written communication. Preferred: prior experience in FDA-regulated manufacturing or lab safety practices.

Qualifications

  • High school diploma or equivalent.
  • Follows written instructions.
  • Basic math and neat, accurate record keeping.
  • Clear speaking and writing.

Responsibilities

  • Operate machines that produce, fill, and seal pouches.
  • Operate heat sealing machines.
  • Load parts and materials into machines and monitor them during operation.
  • Fill and label vials.
  • Operate labeling machines.
  • Package pouches and vials into kits.
  • Account for finished product and materials used.
  • Perform regular inventory counts.
  • Enter production data into the computer system.
  • Fill out production records accurately as work is done.
  • Keep machines and work areas clean, and report machine problems.
  • Notify supervisor when supplies run low.

Skills

Basic math
Record keeping
Clear speaking and writing

Education

High school diploma or equivalent

Job description

Qualigen Diagnostics, Inc. in Carlsbad, CA seeks a Manufacturing Technician for a 2nd shift temporary role to produce FastPack test kits. You will operate filling and sealing machines, label vials, and assemble kits according to FDA-compliant instructions.

Requirements include a high school diploma or equivalent, basic math, neat records, and clear spoken and written communication. Preferred: prior experience in FDA-regulated manufacturing or lab safety practices.

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