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Quality Control
Contract: Atlanta, Georgia, US span>
Salary Range: 24.00 - 26.00 | Per Hour
Job Code: 360088
End Date: 2025-04-18
Job Status: Expired
This Job is no longer accepting applications
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Conduct product testing, including testing to support complaint investigations and stability verification
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Generate product testing results reports
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Review production batch records for accuracy and completeness to approve intermediate products for use in production.
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Review finished goods batch records.
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Report all deviations in these records and assures these have been addressed and resolved prior to issuing approval.
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Conduct spot-checks inspections/audits of production operations
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Participate in the internal audit program
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Write, review and approve Standard Operating Procedures (SOPs) as necessary
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May assist in supporting the Document Control program, record retention areas, and sample retention areas
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May support returned instrument processing
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Log returned instruments from the field.
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Decontaminate returned instruments in a Biohazard level II environment following standard operating procedure and documenting decontamination as required.
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Inspect returned instruments for damage and perform basic investigation and documenting results prior to second level processing.
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As necessary, process instrument documentation for return to repair facility, and pack instruments as required.
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Other duties as assigned by supervisor
- A Bachelor's degree in a scientific or technical field, or an equivalent combination of education and experience. A minimum of one year of experience in a quality assurance role within the medical device industry is preferred.
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Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
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Ability to write routine reports and correspondence.
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Ability to speak effectively before small groups of customers or employees of an organization.
- Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations
- To perform this job successfully, an individual should have knowledge of Database software; Internet software; Inventory software; Spreadsheet software and Word Processing software.
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Ability to follow Good Manufacturing/Laboratory Practices (GMP and GLP)
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Ability to follow procedures and accurately document results
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Understanding the manufacturing processes of Company products and ability to recognize deviations from approved documented procedures.
Job Requirement
- Quality Control Technician
- Quality Control Associate
- Quality Control Specialist
- Quality Control
- QC
- Product Testing
- Inspection
- SOP
- Audits
- Documentation
- Documentation Control
- Batch Record
- Batch Review
- GMP
- GLP
- Medical Device
- Medical Devices
- Pharma
- Pharmaceuticals
- Biotechnology
- Microbiology
Reach Out to a Recruiter
- Recruiter
- Phone
- Deepak Arya
- deepak.arya@collabera.com
This Job is no longer accepting applications
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