Onsite Pharma QA Operations Specialist

Parker Staffing, LLC.; Belle Brook Estates (TN); On-site; USD 34,000 - 41,000; Full time

Benefits offered by this job

Paid time off

Medical, Dental and Vision Insurance

401(k) plans

Full Benefits Summary Available Upon 


Job summary

Parker Staffing, LLC. is seeking an Operations Quality Assurance Technical Specialist for our client’s Bristol, TN site. The role supports production compliance, batch record reviews, and QA activities with authority to stop production if needed.

Qualifications include 3+ years in quality roles, GMP/GLP knowledge, and strong communication. This is a direct hire, onsite opportunity offering a competitive pay rate and comprehensive benefits.

Qualifications

• 3+ years of experience in a Quality related position with GMP/GLP
• 2+ years of processing experience
• Strong interpersonal communication skills
• Ability to work across three shifts when necessary

Responsibilities

• Performs line clearances to ensure documents, equipment and processing areas are ready for processing and changeovers
• Conduct routine audits of manufacturing processes, equipment, and documentation
• Monitor production activities to ensure adherence to procedures
• Verify the accuracy of manufacturing batch records and final sign offs
• Review and approve packaging batch header sheets and labeling
• Ensure SOPs and cGMP compliance on the shop floor
• Collect, analyze and trend quality data for improvements
• Collaborate with departments to implement quality enhancements
• Represent QA on shift to resolve issues
• Utilize SAP, QMS and training programs for change controls and CAPAs
• Write or update SOPs and policies
• Perform other duties as assigned

Skills

Quality assurance

Analytical skills

Communication

Problem solving

Education

Bachelor's degree in scientific field

Tools

SAP

QMS

Microsoft Excel

Job description

Parker Staffing, LLC. is seeking an Operations Quality Assurance Technical Specialist for our client’s Bristol, TN site. The role supports production compliance, batch record reviews, and QA activities with authority to stop production if needed.

Qualifications include 3+ years in quality roles, GMP/GLP knowledge, and strong communication. This is a direct hire, onsite opportunity offering a competitive pay rate and comprehensive benefits.