Quality Control

Contract: Atlanta, Georgia, US

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
To discuss more about this job opportunity, please reach out to Deepak Arya (LinkedIn URL - www.linkedin.com/in/deepak-arya-8a79aa22a/), email your updated resume at Email - deepak.arya@collabera.com or give me a call at (425)-298-1474. Thank you! 
 
Pay range: $24 to $26/hrs 
 
Industry: Biopharma/Medical Devices  
Duration: 12 months  
Working Hours: 2nd Shift (2:30 p.m. to 11:00 p.m.) 
 
Key Responsibilities: 
  • Conduct product testing, including testing to support complaint investigations and stability verification
  • Generate product testing results reports
  • Review production batch records for accuracy and completeness 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-checks 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 perform 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 
Qualifications: 
  • 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. 
Language Skills: 
  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
  • Ability to write routine reports and correspondence.
  • Ability to speak effectively before small groups of customers or employees of an organization. 
Mathematical Skills: 
  • Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations 
Computer Skills: 
  • To perform this job successfully, an individual should have knowledge of Database software; Internet software; Inventory software; Spreadsheet software and Word Processing software.
Skills: 
  • Ability to follow Good Manufacturing/Laboratory Practices (GMP and GLP)
  • Ability to follow procedures and accurately document results
  • 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
  • Email
  • Phone
  • Deepak Arya
  • deepak.arya@collabera.com
This Job is no longer accepting applications
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Collabera is a leading global digital talent solutions firm. For over 25 years, we have provided digital and IT talent services, direct placement and career advisement, global remote talent and learning solutions to transform and diversify workforces for the Fortune 1000 globally.

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