Lonza
QC Analyst II-Microbial Control
US - Portsmouth, NH · Mid
Sponsorship not specifiedDetected 22 days ago
GMPCommunicationCollaborationOrganizational Skills
About the role
- This role is based onsite, where hands-on laboratory work and collaboration are essential to maintaining quality and compliance with cGMP standards.
- This position follows a Sunday-Wednesday schedule, with working hours from 7:30 PM to 5:30 AM.
- With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow.
Responsibilities
- Perform microbiological testing for in-process, release, and stability samples
- Support environmental and utility monitoring, including HVAC and facility sampling
- Review and document test results in accordance with GMP and data integrity standards
- Use laboratory systems and software to record and manage data
- Identify deviations and support investigations when results fall outside expected ranges
- Hands-on training and skill-building
Requirements
- Associate's degree in Microbiology, Biochemistry, or a related science field
- Ability to interpret data and identify trends or deviations
Nice to have
- Experience in a GMP or regulated laboratory environment preferred
- Prior laboratory experience, familiar with aseptic techniques and strong documentation practices, preferred
Compensation
- Competitive pay and performance-based compensation
Benefits
- Medical, dental, and vision insurance
Company info
- What we are looking for
- Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together.
- Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
- If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
This listing is sourced directly from Lonza's careers page and normalized into a canonical job model.