Quality Technician — GMP/GLP Lab Testing

Regulatory Jobs

Illinois

On-site

USD 28,000 - 56,000

Full time

14 days+

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Benefits offered by this job

Free medical coverage
Strong retirement plan
Tuition reimbursement
FreeU education benefit

Job summary

Abbott Park, IL (Lake Bluff area) hosts a Quality Technician who performs bioanalytical and platform quality testing within WWLIMS, QIMS and SAP systems, contributes to CAPA investigations, and maintains product and testing inventory with strict adherence to the quality system.

The role requires working with minimal supervision, redlining documents, reviewing procedures, and executing daily activities while upholding GMP/GLP standards and safety requirements in a high‑paced laboratory setting.

Qualifications

  • Bachelor’s degree (or equivalent) in a science or closely related discipline or relevant equivalent experience
  • Basic computer skills are needed; Advanced Microsoft Word skills a must.
  • Quality testing in a high-paced laboratory environment.
  • Familiarity with GMP/GLP and Abbott QS requirements.

Responsibilities

  • Implement and maintain the effectiveness of the quality system.
  • CAPA investigations and data trending; document and communicate findings.
  • Collaborate within the team and with quality professionals.
  • Maintain relevant documents and records.
  • Perform quality testing in a high-paced laboratory environment.
  • Monitor testing processes and implement improvements within own area.
  • Maintain and update computer systems and related applications.
  • Adhere to GMP/GLP and Abbott Quality System requirements.
  • Provide quality support to processes and product development projects.

Education

Bachelor’s degree (or equivalent) in a science or closely related discipline

Job description

Abbott Park, IL (Lake Bluff area) hosts a Quality Technician who performs bioanalytical and platform quality testing within WWLIMS, QIMS and SAP systems, contributes to CAPA investigations, and maintains product and testing inventory with strict adherence to the quality system.

The role requires working with minimal supervision, redlining documents, reviewing procedures, and executing daily activities while upholding GMP/GLP standards and safety requirements in a high‑paced laboratory setting.

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