Clinical Manufacturing Tech — Early-Phase GMP Specialist

Lonza Group Ltd.; Bend (OR); On-site; USD 70,000 - 110,000; Full time

Job summary

Lonza Group Ltd. in Bend, Oregon seeks individuals to manufacture clinical trial materials in strict GMP compliance. You will operate and maintain manufacturing equipment, own equipment lifecycles, and support tech transfer with cross-functional teams to drive process improvements.

The role emphasizes rigorous documentation, safety, quality, and continuous improvement in a fully site-based manufacturing setting.

Qualifications

• High school diploma or equivalent with relevant industry experience, or a bachelor’s degree in engineering, science, or a related field.
• Experience in pharmaceutical or GMP-regulated manufacturing environments preferred.
• Knowledge of manufacturing equipment and production processes.
• Strong analytical, problem-solving, and organizational skills.
• Excellent attention to detail and commitment to accurate documentation.
• Ability to work effectively in a collaborative team environment.
• Commitment to safety, quality, and continuous improvement.

Responsibilities

• Manufacture clinical trial materials in accordance with approved GMP procedures and quality standards.
• Operate, clean, troubleshoot, and maintain pharmaceutical manufacturing equipment.
• Serve as an equipment owner and support equipment lifecycle, qualification, and maintenance activities.
• Support technology transfer, process optimization, and continuous improvement projects.
• Analyze manufacturing data and provide technical insights to support project objectives.
• Prepare and maintain GMP documentation, including procedures, reports, and training materials.
• Ensure all activities comply with safety, quality, and regulatory requirements.

Skills

Analytical skills

Problem-solving

Attention to detail

Team collaboration

Documentation

Education

Bachelor's degree or higher in engineering/science-related field

Job description

Lonza Group Ltd. in Bend, Oregon seeks individuals to manufacture clinical trial materials in strict GMP compliance. You will operate and maintain manufacturing equipment, own equipment lifecycles, and support tech transfer with cross-functional teams to drive process improvements.

The role emphasizes rigorous documentation, safety, quality, and continuous improvement in a fully site-based manufacturing setting.