Experienced Pharmaceutical Manufacturing Technician

Lonza; Bend (OR); On-site; USD 52,000 - 78,000; Full time

Job summary

Lonza Pharma & Biotech in Bend, Oregon, is seeking an experienced Manufacturing Technician to support clinical manufacturing activities. You will help manufacture materials for clinical trials, operate and maintain process equipment, and contribute to improvement initiatives in a regulated setting.

You will work with cross-functional teams to ensure procedures, documentation, and quality systems meet cGMP standards and safety requirements.

Qualifications

• Experience in pharmaceutical manufacturing environments.
• Ability to own and operate process equipment.
• Familiarity with GMP/cGMP practices and documentation.

Responsibilities

• Manufacture clinical trial materials and support process development.
• Operate, clean, and troubleshoot processing equipment; ensure GDP compliance.
• Support equipment installation, qualification, and change controls.
• Compile technical documentation and support quality systems.

Skills

Pharma manufacturing

Equipment ownership

cGMP knowledge

Education

Bachelor's degree in chemical engineering

High School Diploma or equivalent

Job description

The actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed.

Lonza Pharma & Biotech is hiring an experienced Pharmaceutical Manufacturing Technician for their Early Phase Clinical Manufacturing team.

What You Will Get:

• Opportunity to contribute to the development and manufacture of innovative pharmaceutical products.
• Hands‑on experience supporting clinical manufacturing and product development activities across multiple scales.
• Exposure to cross‑functional teams, including manufacturing, engineering, quality, and technical operations.
• Ownership of manufacturing process equipment and involvement in equipment lifecycle management.
• Opportunities to develop technical expertise in pharmaceutical manufacturing processes and unit operations.
• A collaborative environment that encourages continuous improvement, knowledge sharing, and professional growth.
• Experience working within a regulated cGMP environment that emphasizes safety, quality, and compliance.

Manufacturing & Process Support

• Support pharmaceutical product and process development through the manufacture of clinical trial materials.
• Execute manufacturing activities in accordance with approved procedures and Good Documentation Practices (GDP).
• Establish subject matter expertise in the assembly, operation, cleaning, and troubleshooting of process equipment.
• Perform routine cleaning of manufacturing areas and support maintenance and calibration activities.
• Participate in manufacturing technology transfers and provide technical feedback within areas of expertise.
• Apply an ownership mindset to manufacturing equipment and production spaces.

Engineering Support & Technical Operations

• Assist with equipment installation, startup, commissioning, qualification, and change control activities.
• Support equipment qualification and process improvement initiatives.
• Analyze and interpret process data to support project objectives and informed decision‑making.
• Drive continuous improvement initiatives related to manufacturing processes, equipment, and operational efficiency.

Documentation & Compliance

• Prepare and maintain technical documentation, including SOPs, work instructions, training materials, technical reports, memorandums, and technology transfer documentation.
• Support investigation activities, change controls, and quality system requirements.
• Ensure all work is performed in compliance with cGMP regulations, site procedures, and safety requirements.
• Clearly communicate technical findings and project outcomes to internal stakeholders and clients.

What We Are Looking For:

• High School Diploma or equivalent with relevant industry experience; or bachelor's degree in chemical engineering, engineering, or a related scientific discipline.
• Knowledge of pharmaceutical manufacturing process machinery and unit functions preferred.
• Ability to develop technical expertise and serve as an equipment owner for specific process systems.
• Experience working within a GMP‑regulated environment preferred.
• Strong attention to detail and commitment to documentation accuracy.
• Ability to work effectively in a fast‑paced, team‑oriented environment.
• Strong problem‑solving, analytical, and organizational abilities.
• Commitment to safety, quality, and continuous improvement principles.
• Ability to learn new technologies, processes, and manufacturing techniques.
• Ability to lift materials and equipment as required.
• Comfortable working in a manufacturing environment requiring personal protective equipment (PPE).
• Ability to safely work with and around hazardous chemicals while following established safety procedures.