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Quality Control Technician

Experis/Manpower Group

Atlanta, GA

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JOB DETAILS
SALARY
$22–$26 Per Hour
SKILLS
Document Control, Documentation, Fortune 500 Customers, GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), Internal Audit, Medical Equipment, Operational Audit, Product Testing, Quality Assurance, Quality Control, Retention Programs, Returns Processing, Standard Operating Procedures (SOP), Support Documentation, Testing
LOCATION
Atlanta, GA
POSTED
Today
Title: Quality Control Technician
Location: Atlanta GA (100% Onsite)
Duration: 12 Months
Shift Time: 8am to 5pm
Pay Range : $22/hr to $26/hr (On W2)

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

Job Responsibilities:
  • Conduct product testing, including testing to support complaint investigations and stability verification
  • Generate product testing results reports
  • Review production batch records (DHR's) for accuracy and completeness in order to approve intermediate products for use in production.
  • Review finished goods batch records.
  • Report all deviations in these records and assures these have been addressed and resolved prior to issuing approval.
  • Conduct spot-check inspections/audits of production operations
  • Participate in the internal audit program
  • Write, review and approve Standard Operating Procedures (SOPs) as necessary
  • May assist in supporting the Document Control program, record retention areas, and sample retention areas
  • May support returned instrument processing
  • Log returned instruments from the field.
  • Decontaminate returned instruments in a Biohazard level II environment following standard operating procedure and documenting decontamination as required.
  • Inspect returned instruments for damage, and performing basic investigation and documenting results prior to second level processing.
  • As necessary, process instrument documentation for return to repair facility, and pack instruments as required.
  • Other duties as assigned by supervisor Supervisory Responsibilities This job has no supervisory responsibilities.
  • The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Ability to follow Good Manufacturing/Laboratory Practices (GMP and GLP
Education:
  • Education and/or Experience Bachelor's degree in a scientific or technical area or equivalent combination of experience and education.
  • At least one year in quality assurance role in medical device industry is preferred.

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

If you're interested, please click "Apply" button

About the Company

E

Experis/Manpower Group

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