QC Batch Review Technician (Biotechnology)

Location: On-site in Pensacola, Florida, United States; working hours are 11:00 a.m. to 7:00 p.m.

Company

Cytiva is a hirify.global operating company providing life-science, diagnostics, and biotechnology solutions that support biological research, vaccines, medicines, and cell and gene therapies.

What you will do

• Review raw material, intermediate, and finished-good records for timely, accurate, and compliant product release.
• Conduct incoming raw material inspections and finished batch release activities under ISO 9001 and Cytiva QMS requirements.
• Verify Good Documentation Practices, collect samples, perform basic product testing, and confirm documentation completeness.
• Initiate nonconformance records, manage blocked and released stock activities, and participate in investigations when appropriate.
• Maintain release logs, support internal compliance audits at GEMBA, and coordinate improvements with Production and Supply Chain.

Requirements

• Bachelor’s degree in Science or Engineering.
• Ability and willingness to become proficient in tracking and trending data in Excel.
• Ability to manage simultaneous assignments with strong attention to detail.
• Reliable transportation and a good driving record for travel between local sites if needed.
• Ability to lift, push, pull, or carry equipment weighing up to 50 lb and perform tasks requiring fine motor skills and depth perception.

Nice to have

• 0–3 years of Quality Assurance experience in an ISO 9001-regulated environment.
• Quality Assurance or Quality Control experience in a GLP, GMP, or ISO 9001 biotechnology or pharmaceutical company.
• Experience building strong working relationships with other departments.

Culture & Benefits

• Paid time off.
• Medical, dental, and vision insurance for eligible employees.
• 401(k) plan for eligible employees.
• Continuous improvement culture focused on life-science innovation and tangible impact.