Bioprocess Manufacturing Technician — cGMP & Impact

Lonza; Vacaville (CA); On-site; Confidential; Full time

Benefits offered by this job

Performance-related bonus

Medical, dental and vision insurance

401(k) matching plan

Life insurance, as well as short-term/

Job summary

Lonza in Vacaville, CA is seeking a Manufacturing Technician – Bioprocess to join a production team dedicated to high-quality biotherapeutic medicines. This site-based role emphasizes real-time collaboration and strict cGMP compliance.

You will operate and maintain automated production systems, manage inventory, and support upstream and downstream processing, while ensuring safety and precise documentation. A strong attention to detail and teamwork are essential.

Qualifications

• High School Diploma or GED Required.
• AS/BS/BA in Biological Sciences, Physical Sciences, or Engineering preferred.
• Proven ability to work in a fast-paced, regulated environment.
• Strong attention to detail and flawless documentation practices.
• Ability to determine and implement solutions to process issues.
• Excellent collaboration and communication skills.

Responsibilities

• Operate and maintain production systems in a cGMP environment, ensuring inspection readiness and regulatory compliance.
• Manage inventory and process systems, maintaining accurate records and safety protocols.
• Participate in production of mammalian cell culture products across upstream and downstream areas.
• Perform dispensing of components, handle hazardous materials, and clean/sterilize equipment.
• Support Right-First-Time operations with thorough documentation and issue resolution.
• Use automation for production tasks and collaborate with the team to meet production demands.

Skills

Detail oriented

Teamwork

Documentation

Problem solving

Education

High School Diploma or GED

AS/BS/BA in Biological Sciences, Physical Sciences, or Engineering

Job description

Lonza in Vacaville, CA is seeking a Manufacturing Technician – Bioprocess to join a production team dedicated to high-quality biotherapeutic medicines. This site-based role emphasizes real-time collaboration and strict cGMP compliance.

You will operate and maintain automated production systems, manage inventory, and support upstream and downstream processing, while ensuring safety and precise documentation. A strong attention to detail and teamwork are essential.