Quality Control Technician — GMP Audits & Lab Sampling

OSI Group; Tipton (IN); On-site; USD 20,664,000 - 27,552,000; Full time

Benefits offered by this job

Overtime eligibility

401k matching

Paid time off

Job summary

OSI Group in Tipton, Indiana is seeking a production QA/Line Auditor to perform a variety of line audits and tests to ensure product quality and compliance with production and sanitary procedures. You will monitor temperatures, test metals, collect samples, and maintain documentation across shifts.

The role requires attention to detail, adherence to GMP, PPE usage, and ability to work with lab instructions and records. Overtime may be offered based on production needs and shift timing.

Qualifications

• 3 months of on the job training.

Responsibilities

• Audit line internal temperature of cooked products; record.
• Audit metal detectors with the use of standards; if detector is faulty, retain product and re-test product made since last successful test.
• Perform line audits, recording speed, temperature, weights.
• Perform weekly swabs of equipment/gloves and plates of air; package with instructions and send to lab.
• Gather cooked and raw product samples to send to lab with testing instructions.
• Maintain and test shelf life samples; perform organoleptic duties.
• Inspect code dates on bags, boxes, and cases based on product specification and production schedule.
• Inspect and record cooler and freezer temperatures.
• Cook samples 2-3 times per shift from all lines.
• Perform hourly piece count of packed box.
• Calibrate scales and thermometers daily.
• Complete paperwork on employee sanitation compliance.
• Follow all safety rules.
• Use PPE; practice GMP.
• Keep assigned area clean.
• Perform other duties as assigned.

Skills

On-the-job training

Job description

OSI Group in Tipton, Indiana is seeking a production QA/Line Auditor to perform a variety of line audits and tests to ensure product quality and compliance with production and sanitary procedures. You will monitor temperatures, test metals, collect samples, and maintain documentation across shifts.

The role requires attention to detail, adherence to GMP, PPE usage, and ability to work with lab instructions and records. Overtime may be offered based on production needs and shift timing.