QA Technician II, Cell Therapy Operations

Cellipont Bioservices; The Woodlands (TX); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Career growth

401K match

Tuition reimbursement

Employee referrals

Flexible PTO

Pet coverage

Job summary

Cellipont Bioservices is seeking a QA Technician II, Operations to support GMP manufacturing of master/working cell banks and provide on-the-floor QA oversight. The role includes real-time documentation review, room release and issue resolution to ensure compliance.

You will participate in root-cause analysis and contribute to process improvements while guiding GMP practices across teams. The ideal candidate will have a bachelor's degree with 1–2 years in GMP environments, familiarity with cell

Qualifications

• Bachelor's degree preferred with 1–2 years of GMP experience.
• Exposure to manufacturing processes related to cell therapy.
• Analytical, problem-solving and decision-making skills.

Responsibilities

• Performs QA on-the-floor activities supporting client projects, including room release and reviewing documentation in real time.
• Audits manufacturing and support areas, reviewing batch records for adherence to procedures and best practices.
• Review and disposition batch records for completeness and compliance; act as first responder to quality issues on the floor.
• Participates in root-cause analysis using methodologies (fishbone, 5 whys, etc.).
• Support evaluation and lot disposition of cell therapies; write and revise GMP documents as needed.

Skills

Analytical skills

Troubleshooting

Decision-making

Teamwork

Problem solving

Education

Bachelor's degree

Tools

Microsoft Access

Excel

Microsoft Office

Job description

Cellipont Bioservices is seeking a QA Technician II, Operations to support GMP manufacturing of master/working cell banks and provide on-the-floor QA oversight. The role includes real-time documentation review, room release and issue resolution to ensure compliance.

You will participate in root-cause analysis and contribute to process improvements while guiding GMP practices across teams. The ideal candidate will have a bachelor's degree with 1–2 years in GMP environments, familiarity with cell