Experienced Microbiologist
Lonza
Summary
Join Lonza Pharma & Biotech in Bend, Oregon, as an Experienced Microbiologist. In this role, you will contribute to the development and manufacture of life-changing therapies while working alongside a collaborative team in a highly regulated laboratory environment.
Job description
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will do
- Design, validate, and transfer microbiological testing methods in compliance with regulatory and quality standards.
- Support testing and release activities for raw materials, in-process materials, and finished products.
- Lead environmental monitoring activities and analyze data to help reduce contamination risks.
- Maintain, qualify, and troubleshoot laboratory equipment to ensure reliable results.
- Author, review, and approve technical documents, including protocols, procedures, and reports.
- Support audit readiness and represent the microbiology function during inspections and client visits.
- Mentor team members and drive continuous improvement initiatives across the laboratory.
What we are looking for
- Bachelor's degree in Microbiology, Biology, or another related scientific discipline.
- Experience working in a pharmaceutical, biotechnology, or other regulated laboratory environment.
- Knowledge of microbiological techniques, including bioburden, sterility, and endotoxin testing.
- Experience with environmental monitoring in cleanroom or controlled manufacturing environments.
- Understanding of current Good Manufacturing Practices (cGMP) and quality requirements.
- Experience supporting validation, qualification, or contamination control activities.
- Availability to work a 4x10-hour shift schedule that includes one weekend day.
Requirements
- Bachelor's degree in Microbiology, Biology, or another related scientific discipline.
- Experience working in a pharmaceutical, biotechnology, or other regulated laboratory environment.
- Knowledge of microbiological techniques, including bioburden, sterility, and endotoxin testing.
- Experience with environmental monitoring in cleanroom or controlled manufacturing environments.
- Understanding of current Good Manufacturing Practices (cGMP) and quality requirements.
- Experience supporting validation, qualification, or contamination control activities.
- Availability to work a 4x10-hour shift schedule that includes one weekend day.
Benefits
- Medical, Dental & Vision
- Relocation assistance
- Professional growth opportunities
- Career development
- Collaborative team environment
Company overview
Lonza is a pioneering global Contract Development and Manufacturing Organization (CDMO) and a world leader in pharmaceutical manufacturing services. Founded in 1897 in Switzerland, the company has evolved into the first and original CDMO, now operating as one of the largest Western CDMO networks with approximately 19,000 employees across more than 30 sites spanning five continents. Lonza specializes in transforming therapeutic discoveries into life-saving and life-enhancing treatments for patients worldwide. The company's comprehensive services span from early development to drug substance and drug product manufacturing, covering established and emerging technologies including mammalian biologics, small molecules, highly potent APIs, bioconjugates, mRNA, microbial products, and cell and gene therapies. With a focus on cutting-edge science, smart technology, and lean manufacturing, Lonza serves a diverse customer base ranging from emerging biotechs to global pharmaceutical companies, delivering integrated solutions throughout the entire treatment lifecycle.