Sterile QA Specialist — cGMP/Aseptic Expert

Akraya, Inc.; Greenville (NC); On-site; USD 72,000 - 77,000; Full time

Job summary

Akraya, Inc. is seeking a Quality Assurance/Quality Control professional for a 10-month, W2 contract in Greenville, NC.

The role focuses on driving quality execution across sterile operations, including manufacturing, filling, packing, and inspection, with emphasis on process improvements. The position requires a Bachelor's degree in technology/engineering/microbiology, 4+ years in QA/QC/manufacturing, strong data analysis and troubleshooting skills, and solid technical writing abilities.

Qualifications

• Bachelor's degree in technology, engineering, or microbiology.
• 4+ years in Quality Assurance, Quality Control, or Manufacturing.
• Data analysis and troubleshooting expertise.
• Strong ownership and leadership abilities.
• Technical writing experience.
• Physical ability to work production floor (standing, walking, bending for prolonged periods).

Responsibilities

• Perform daily quality assessments of facility, personnel, and documentation to ensure compliance with cGMPs
• Interact with employees on troubleshooting, documentation, and aseptic technique guidance
• Champion quality culture and support continuous improvement initiatives
• Participate in deviation event response and Root Cause Analysis
• Review and approve procedures, training documents, deviations, and change controls
• Perform quality batch record review

Skills

Bachelor's degree

Quality Assurance

Quality Control

Manufacturing

Data analysis

Troubleshooting

Ownership

Leadership

Technical writing

Physical stamina

Education

Bachelor's degree in technology/engineering/microbiology

Job description

Akraya, Inc. is seeking a Quality Assurance/Quality Control professional for a 10-month, W2 contract in Greenville, NC.

The role focuses on driving quality execution across sterile operations, including manufacturing, filling, packing, and inspection, with emphasis on process improvements. The position requires a Bachelor's degree in technology/engineering/microbiology, 4+ years in QA/QC/manufacturing, strong data analysis and troubleshooting skills, and solid technical writing abilities.