Mid-Shift Production Technician (GMP/ISO)

Accelera

Columbus (NE)

On-site

USD 28,000 - 30,000

Full time

24 hours ago
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Job summary

Accelera in Columbus, NE seeks a Contract Production Technician for a five-month assignment with a mid-shift schedule (4:00 PM–12:00 AM), Monday–Friday. On-site interview and steel-toe footwear are required. Responsibilities include reprocessing, parts management, quality checks, packaging, and logging activities, following FDA/GMP/ISO standards. Must rotate through duties and maintain records with accuracy.

Qualifications

  • High school diploma or equivalent.
  • Ability to read and understand technical instructions in English.
  • Basic math skills are required.
  • Detail-oriented with strong record-keeping abilities.
  • Ability to rotate through stations and work with teammates.
  • Willingness to work a mid-shift schedule and accommodate overtime as needed.

Responsibilities

  • Execute product reprocessing and parts management per protocols.
  • Perform visual inspections and use basic measurement tools for quality.
  • Pack, label, and ensure correct packaging of items.
  • Maintain production records and logs with accuracy.
  • Follow SOPs and work instructions.
  • Support regulatory compliance through proper recordkeeping (FDA/GMP/ISO).
  • Collaborate to meet daily production targets.
  • Rotate through stations and adapt to changing needs.
  • Maintain a tidy, hazard-free workspace and safety practices.
  • Demonstrate reliable attendance and shift flexibility.

Skills

Attention to detail
Teamwork
Reliability
English literacy
Basic math
Safety awareness
Flexibility
Adaptability

Education

High school diploma or equivalent

Tools

Basic measurement tools

Job description

Accelera in Columbus, NE seeks a Contract Production Technician for a five-month assignment with a mid-shift schedule (4:00 PM–12:00 AM), Monday–Friday. On-site interview and steel-toe footwear are required. Responsibilities include reprocessing, parts management, quality checks, packaging, and logging activities, following FDA/GMP/ISO standards. Must rotate through duties and maintain records with accuracy.
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