Quality Control Technician

Experis Technology Group; Alpharetta (GA); On-site; USD 33,000 - 36,000; Full time

Job summary

ManpowerGroup Global, Inc. is seeking a Quality Assurance Specialist to support GMP/GLP-compliant activities in a manufacturing setting.

The role involves product testing, batch record reviews, audits, and SOP development to ensure Quality Management System compliance.

Qualifications

• Bachelor's degree in a scientific or technical field or equivalent experience.
• 1+ year of quality assurance experience in manufacturing or medical device industry.
• GMP and GLP knowledge.
• Ability to follow procedures and document results.
• Understanding of manufacturing processes and deviation handling.
• Strong attention to detail and documentation skills.
• Ability to use bleach for cleaning and decontamination.
• Strong written and verbal communication skills.

Responsibilities

• Perform product testing and stability verification.
• Generate and document testing results and reports.
• Review production batch records (DHRs) for accuracy and completeness.
• Review finished goods batch records and identify deviations.
• Ensure deviations are addressed before product approval.
• Conduct audits and participate in internal audits.
• Write, review, and approve SOPs as needed.
• Support document control, retention, and sample retention.

Skills

Quality Assurance

GMP and GLP knowledge

Documentation skills

Audit experience

Bleach handling

Education

Bachelor's degree in scientific or technical field

Tools

Databases

Spreadsheets

Inventory systems

Word processing

Job description

We are seeking a Quality Assurance Specialist to support Quality Management System activities within a manufacturing environment. This role will perform product testing, batch record review, production audits, documentation, and quality-related activities while ensuring compliance with GMP and GLP requirements.
Pay Rate: $24- $26//hour
Location: Atlanta, GA
Shift: 2:30 PM
Contract: 6 + month

Key Responsibilities

• Perform product testing, including testing related to complaint investigations and stability verification.
• Generate and document product testing results and reports.
• Review production batch records (DHRs) for accuracy and completeness.
• Review finished goods batch records and identify deviations.
• Ensure deviations are properly addressed and resolved before product approval.
• Conduct spot-check inspections and audits of production operations.
• Participate in the internal audit program.
• Write, review, and approve SOPs as needed.
• Support document control, record retention, and sample retention activities.
• Process returned instruments, including:
  • Log instruments returned from the field.
  • Decontaminate returned instruments in a Biohazard Level II environment according to SOPs.
  • Inspect returned instruments for damage and document findings.
  • Support basic investigations and prepare documentation for repair processing.
  • Package instruments for shipment to repair facilities when required.
• Perform other duties as assigned by the supervisor.

Qualifications

• Bachelor's degree in a scientific or technical field, or an equivalent combination of education and experience.
• 1+ year of Quality Assurance experience, preferably within the medical device industry.
• Knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Ability to accurately follow procedures and document results.
• Understanding of manufacturing processes and ability to identify deviations from approved procedures.
• Strong attention to detail and documentation skills.
• Ability to use bleach for cleaning and decontamination purposes.
• Strong written and verbal communication skills.
• Comfortable working with databases, spreadsheets, inventory systems, word processing software, and internet-based applications.