Skills
Microbiology testing
Environmental monitoring
GMP documentation
About the Role
Join Catalent’s Chelsea facility, a global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacturing and packaging. In this Quality Control Analyst I (Microbiology) role, you will support GMP operations through environmental/utilities monitoring and microbiological testing.
Responsibilities
- Perform routine and non-routine environmental and utilities monitoring activities
- Conduct microbiological testing of samples in accordance with established SOPs
- Support GMP manufacturing by generating accurate, timely test results
- Follow cGMP and quality system expectations to maintain compliance
Requirements
- Experience or coursework in microbiology and/or environmental monitoring
- Ability to follow SOPs and documentation requirements with strong attention to detail
- Comfort working in a regulated laboratory environment
- Availability for Monday–Friday, 8:00am–5:00pm onsite schedule
Benefits
- Onsite role at a leading inhaled powder manufacturing Center of Excellence
- Full-time schedule with standard weekday hours
- Opportunity to contribute to GMP quality and patient-focused manufacturing
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