Experienced Pharmaceutical Manufacturing Technician

Lonza•Bend, OR

8d•Onsite

About The Position

Lonza Pharma & Biotech has an opening for an experienced Pharmaceutical Manufacturing Technician to join their Early Phase Clinical Manufacturing team. This role offers the outstanding opportunity to contribute to world-class pharmaceutical innovations, while working in a collaborative and inclusive environment. If you are ambitious and driven by the desire to make a meaningful impact, we want you to join our mission to improve lives. Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

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.

Responsibilities

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.
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.
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.