Experienced Pharmaceutical Manufacturing Technician

Location:

Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed.

Lonza Pharma & Biotech is seeking an experienced Pharmaceutical Manufacturing Technician to join the Early Phase Clinical Manufacturing team. You will support the development and manufacturing of clinical trial materials in a cGMP regulated environment.

• 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:
  Manufacture clinical trial materials, execute activities per approved procedures and Good Documentation Practices.
• Support pharmaceutical product and process development through manufacturing of clinical trial materials.
• Establish subject‑matter expertise in assembly, operation, cleaning and troubleshooting of process equipment.
• Perform routine cleaning of manufacturing areas and assist with maintenance and calibration.
• Participate in manufacturing technology transfers and provide technical feedback.
• 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 decision‑making.
• Drive continuous improvement initiatives related to manufacturing processes, equipment, and operational efficiency.
• Documentation & Compliance:
  Prepare and maintain technical documentation such as SOPs, Work Instructions, Training Materials, Technical Reports, Memoranda, 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.
• Communicate technical findings and project outcomes to internal stakeholders and clients.

• 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.
• 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 using personal protective equipment (PPE) and working safely with hazardous chemicals.

Lonza is an equal‑opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.