What are the responsibilities and job description for the QA Shop Floor Operator position at Source One Technical Solutions?
Source One is a consulting services company and we’re currently looking for the following individual to work as a consultant to our direct client, a global medical device company in Fort Worth, TX.
Job Title: QA Shop Floor Operator (Contract)
Pay Range: $25/hr - $30/hr
40 hours/week, Mon-Fri
This QA Operations Operator role is essentially an entry- to mid-level Quality Assurance floor support position in a regulated manufacturing environment. The person will spend most of their time on the production floor ensuring procedures are followed, documentation is accurate, and quality issues are identified before products move to the next stage. Responsibilities:
Shop Floor Quality Support
• Perform routine quality checks during manufacturing operations.
• Observe production activities to ensure operators follow approved procedures and work instructions.
• Verify that manufacturing processes comply with SOPs, batch records, and quality standards.
• Support production teams while maintaining an independent quality perspective.
Documentation Review
• Review manufacturing records, logbooks, batch records, and production paperwork for completeness and accuracy.
• Verify entries are properly documented, signed, dated, and compliant with GxP requirements.
• Identify documentation errors and work with production personnel to correct them.
Product Inspection and Monitoring
• Monitor products and materials throughout the manufacturing process.
• Perform visual inspections and quality checks.
• Identify defects, discrepancies, or non-conforming materials.
• Escalate quality concerns to QA leadership for investigation.
Deviation and Compliance Support
• Recognize situations where procedures were not followed.
• Report and document deviations, quality events, or compliance issues.
• Assist with investigations by gathering information and supporting documentation.
GMP/GxP Compliance
• Follow Good Manufacturing Practices (GMP) and other GxP requirements.
• Maintain a high level of documentation accuracy and data integrity.
• Complete required training and stay current on procedures.
Requirements:
• GMP/GxP experience
• SOP adherence
• Documentation accuracy
• Attention to detail
• Manufacturing experience
• Quality mindset
Preferred:
• Batch record review
• FDA-regulated environment
• Pharmaceutical or biotech experience
• Deviation identification
• CAPA awareness
• ERP or quality system experience
Salary : $25 - $30