QC Analyst Lvl 2 - Environmental Monitoring
Lonza
Summary
As a QC Analyst II, Microbial Control, you will play an important role in supporting the release of life-changing therapies by performing quality testing that ensures product safety, quality, and compliance. This position offers the opportunity to work in a GMP-regulated laboratory environment, collaborate with cross-functional teams, and contribute directly to manufacturing operations and customer programs.
Job description
This is a fully site-based role with a 10 hour schedule from 7:00 AM to 5:00 PM, Sunday - Wednesday. Includes weekend pay differential.
What you will do
- Perform microbiological testing to support in-process, lot release, and stability programs
- Support utility, environmental monitoring, and cleanroom testing activities
- Review laboratory results to ensure data accuracy, quality, and compliance
- Document testing activities using laboratory systems and GMP documentation practices
- Investigate atypical results and support corrective actions as needed
- Partner with Quality, Manufacturing, and site teams to support operational goals
- Maintain compliance with safety, quality, and regulatory requirements
What we are looking for
- Associate's or Bachelor's degree in Microbiology, Biology, Biochemistry, or a related scientific field, or equivalent experience
- Experience working in a Quality Control laboratory or GMP-regulated environment
- Knowledge of microbiological testing techniques and laboratory practices
- Strong attention to detail and ability to follow established procedures
- Effective written and verbal communication skills
- Ability to prioritize workload and manage multiple responsibilities
- Commitment to quality, safety, and continuous improvement
Requirements
- Associate's or Bachelor's degree in Microbiology, Biology, Biochemistry, or a related scientific field, or equivalent experience
- Experience working in a Quality Control laboratory or GMP-regulated environment
- Knowledge of microbiological testing techniques and laboratory practices
- Strong attention to detail and ability to follow established procedures
- Effective written and verbal communication skills
- Ability to prioritize workload and manage multiple responsibilities
- Commitment to quality, safety, and continuous improvement
Benefits
- Medical, Dental & Vision
- Weekend Pay Differential
- Career Growth Opportunities
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.