Quality Control Technician

Experis; Des Plaines (IL); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading company is seeking a Quality Control Technician for a 12-month contract in Des Plaines, Illinois. The role involves conducting product testing, reviewing production records, and ensuring compliance with quality standards. Candidates should have a scientific background and experience in quality assurance, particularly in the medical device industry.

Qualifications

• Bachelor's degree in a scientific or technical field or equivalent experience.
• At least one year in a quality assurance role in the medical device industry preferred.

Responsibilities

• Conduct product testing and generate testing results reports.
• Review production batch records for accuracy and completeness.
• Write, review, and approve Standard Operating Procedures (SOPs).

Skills

Quality Management System

Good Manufacturing Practices

Good Laboratory Practices

Documentation

Education

Bachelor's degree in a scientific or technical field

Tools

Database software

Spreadsheet software

Word processing software

Job description

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Title: Quality Control Technician

Location: Des Plaines, Illinois (Onsite)

Duration: 12 Months

Pay Range : $20/hr to $24/hr (On W2)

We are looking for a Quality Control Technician to join one of our Fortune 500 clients.

Job Summary
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Understand the manufacturing processes of Company products and recognize deviations from approved documented procedures.

Top Skills

• Perform activities to support the Quality Management System.
• Follow Good Manufacturing/Laboratory Practices (GMP and GLP).
• Read and interpret safety rules, operating and maintenance instructions, and procedure manuals. Write routine reports and correspondence.

Job Responsibilities

• Conduct product testing, including testing for complaint investigations and stability verification.
• Generate product testing results reports.
• Review production batch records (DHRs) for accuracy and completeness to approve intermediate products for use in production.
• Review finished goods batch records.
• Report deviations and ensure they are addressed before approval.
• Conduct spot-check inspections/audits of production operations.
• Participate in the internal audit program.
• Write, review, and approve Standard Operating Procedures (SOPs).
• Support Document Control, record retention, and sample retention areas.
• Support returned instrument processing and log returned instruments.
• Decontaminate returned instruments in a Biohazard Level II environment following SOPs.
• Inspect returned instruments for damage and document findings.
• Process instrument documentation for return to repair facilities and pack instruments as required.

Education And/or Experience

• Bachelor's degree in a scientific or technical field or equivalent experience.
• At least one year in a quality assurance role in the medical device industry is preferred.

Other Skills And Abilities

• Follow procedures and accurately document results.
• Use bleach for cleaning purposes.
• Knowledge of database, internet, inventory, spreadsheet, and word processing software.
• Ability to sit, stand, and walk as required.

We are looking for candidates eligible to work with any employer without sponsorship.

If interested, please click “Apply”.

Seniority level

• Entry level

Employment type

• Contract

Job function

• Quality Assurance

Industries

• Staffing and Recruiting

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