Viral Vector QA Specialist II - Onsite Houston

Lonza; Houston (TX); On-site; Confidential; Full time

Benefits offered by this job

Performance-related bonus

401(k) matching plan

Employee assistance programs

Paid time off (PTO)

Job summary

Lonza in Houston, Texas is seeking a Quality Assurance Specialist II - Viral Vector to oversee QA for viral vector and cell therapy manufacturing, ensuring products meet quality standards.

This onsite role collaborates with Manufacturing, Quality Control, and Engineering to support production, maintain cGMP compliance, and drive continuous improvement, with a Sunday through Thursday shift (7:00 AM - 3:30 PM) and opportunities for growth.

Qualifications

• Associates degree in Life Sciences, Engineering, or a related scientific discipline.
• Experience in GMP-regulated biopharmaceutical or viral vector manufacturing.
• Hands-on cleanroom and gowning experience in classified environments.
• Excellent attention to detail when reviewing GMP documentation and batch records.
• Strong communication and cross-functional collaboration skills.

Responsibilities

• Provide quality oversight for viral vector and cell therapy manufacturing operations, ensuring cGMP compliance.
• Support manufacturing floor activities with QA presence on the floor.
• Perform QA walkthroughs and investigate quality/compliance issues.
• Support investigations, deviations, CAPAs, change controls, and quality system processes.
• Ensure ISO, GMP, and regulatory compliance and maintain inspection readiness.
• Perform cleanroom activities requiring Level 3 gowning (Grade B).
• Maintain quality records tracking and drive continuous improvement.

Skills

Strong communication skills

Problem-solving skills

Cross-functional collaboration

Education

Associates degree in Life Sciences, Engineering, or a related scientific discipline

Job description

Lonza in Houston, Texas is seeking a Quality Assurance Specialist II - Viral Vector to oversee QA for viral vector and cell therapy manufacturing, ensuring products meet quality standards.

This onsite role collaborates with Manufacturing, Quality Control, and Engineering to support production, maintain cGMP compliance, and drive continuous improvement, with a Sunday through Thursday shift (7:00 AM - 3:30 PM) and opportunities for growth.