Experienced Pharmaceutical Manufacturing Technician

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

About the role

Lonza Pharma & Biotech has an opening for an experienced Pharmaceutical Manufacturing Technician to join their Early Phase Clinical Manufacturing team. This role offers the opportunity to contribute to world-class pharmaceutical innovations while working in a collaborative and inclusive environment.

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.

Responsibilities

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:
  • Standard Operating Procedures (SOPs)
  • Work Instructions
  • Training Materials
  • Technical Reports
  • Memorandums
  • 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.

Requirements

• 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.