Night Quality Inspector – Medical Devices (GMP)

MillenniumSoft Inc

Sumter (SC)

On-site

USD 28,000 - 41,000

Part time

9 days ago
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Job summary

MillenniumSoft Inc. is seeking a Quality Inspector for a 5-month contract in Sumter, SC. The role runs 8 PM to 8 AM on a 3-2-2-3 schedule with a 40-hour work week and pay rate of $20–$30 per hour. Requires a high school diploma and 1–2 years in quality control. Eye/vision exams may be required.

The position involves visual, dimensional, and functional inspections of medical device products, maintaining records, and ensuring GMP compliance. It is a contract W2 role; US citizens or GC holders only.

Qualifications

  • High school diploma or GED required.
  • 1–2 years of related Quality Control experience preferred.
  • Demonstrated interpersonal and communications skills.
  • Ability to read and comprehend English.
  • Ability to lift up to 50 lbs.

Responsibilities

  • Performs visual, dimensional and functional inspections on a wide variety of products.
  • Reports non-conformances to Supervisor and advises corrective action.
  • Follows up to verify effectiveness of corrective actions.
  • Decides whether product is acceptable or rejected and maintains inspection records.
  • Recognizes conditions outside inspection area and refers items to supervisor.
  • Ensures GMP compliance in working areas and reports infractions.
  • Evaluates product and process during visual inspections and makes decisions.
  • Responsibilities impact product quality, productivity, and costs.

Skills

Quality control
Communication skills
Reading English
Lifting up to 50 lbs

Education

High school diploma or GED

Job description

MillenniumSoft Inc. is seeking a Quality Inspector for a 5-month contract in Sumter, SC. The role runs 8 PM to 8 AM on a 3-2-2-3 schedule with a 40-hour work week and pay rate of $20–$30 per hour. Requires a high school diploma and 1–2 years in quality control. Eye/vision exams may be required.

The position involves visual, dimensional, and functional inspections of medical device products, maintaining records, and ensuring GMP compliance. It is a contract W2 role; US citizens or GC holders only.

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