Quality Control Technician
1300 East Touhy Ave Des Plaines Illinois USA 60018-3315
12-month contract with high possibility of extension
Pay rate: $20-25/hr.

Hi $first name$,

My name is Sukanya Rednam, and I am Recruitment Specialist at Experis - The Manpower Group. I am recruiting for an immediate job opportunity with one of our direct clients. If you are interested in the below mentioned opportunity, then you can give me a call at 414-644-8036 or you can respond me with the updated copy of your resume on my email ID that is rednam.sukanya@experis.com.

Position Details:

Title: Quality Control Technician

Location: Des Plaines IL(Onsite)

Duration: 12 Months Contract to Hire

Payrate : $25/hr on w2

Job Description:

The Quality Assurance Technician performs various tasks to support the Quality Management System, ensuring compliance with Good Manufacturing/Laboratory Practices (GMP and GLP) in the medical device industry. Responsibilities include conducting product testing, reviewing production batch records, participating in internal audits, and supporting document control activities.

Essential Duties and Responsibilities:

Conduct product testing, including tests to support complaint investigations and stability verification.
Generate product testing results reports.
Review production batch records for accuracy and completeness, approving intermediate products for production use and ensuring resolution of deviations.
Conduct spot-check inspections and audits of production operations.
Participate in the internal audit program.
Write, review, and approve Standard Operating Procedures (SOPs) as necessary.
Assist in supporting the Document Control program, record retention areas, and sample retention areas.
Support returned instrument processing, including logging, decontamination, inspection, and documentation.
Perform other duties as assigned by the supervisor.
Qualifications:

Bachelor's degree in a scientific or technical area preferred, or equivalent combination of experience and education.
At least one year of experience in a quality assurance role in the medical device industry preferred.
Ability to follow GMP and GLP guidelines.
Proficiency in reading and interpreting documents, writing reports, and speaking effectively.
Strong mathematical skills for practical applications.
Proficiency in database, internet, inventory, spreadsheet, and word processing software.
Attention to detail and ability to accurately document results.
Understanding of manufacturing processes and ability to recognize deviations.

We are looking for the candidate who are eligible to work with any employers without sponsorship .

If you're interested, please click “Apply” button.