- Lonza Walkersville Inc
- US,
- Full-Time
- 10 days ago
QC Analyst I-Microbial Control.
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QC Analyst I-Microbial Control: our view in 3 lines...
- The Role:This role is for a QC Analyst supporting microbial control in a pharmaceutical manufacturing site.
- The Person:The person will perform microbiological testing, support environmental and utility monitoring, record results, manage data in laboratory systems, and help identify and escalate deviations while following GMP and data integrity standards.
- Requirements:The ideal candidate has an Associate’s degree in Microbiology, Biochemistry, or a related science field, with limited experience in a laboratory or regulated environment and a basic understanding of laboratory techniques and aseptic practices.
About the role
Job Title: Quality Control Analyst I – Microbial Control
Location: Portsmouth, NH, (On-site)
As a QC Analyst I in Microbial Control at our Portsmouth site, you will support microbiological testing and monitoring activities to help ensure the safety and quality of drug products. You will assist with laboratory testing, environmental monitoring, and documentation while working under the guidance of experienced team members. This role is based onsite, where hands-on laboratory work and collaboration are essential to maintaining quality and compliance with cGMP standards.
The position follows a Wednesday through Saturday schedule, working overnight from 8:30 PM to 7:00 AM. Shift differentials are offered for Nights and Weekends worked.
What you will get
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Competitive pay and performance-based compensation
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Medical, dental, and vision insurance
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A supportive and inclusive work environment
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Opportunities for career growth and development
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Hands-on training and skill-building
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A collaborative and team-focused laboratory environment
What you will do
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Perform microbiological testing for in-process, release, and stability samples with guidance
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Support environmental and utility monitoring, including HVAC and facility sampling
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Record and document test results following GMP and data integrity standards
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Use laboratory systems and basic software to enter and manage data
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Assist in identifying deviations and escalate issues to senior team members
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Follow cGMP, GDP, and data integrity requirements in all assigned tasks
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Participate in routine lab activities, including sample handling and cleaning
What we are looking for
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Associate’s degree in Microbiology, Biochemistry, or a related science field
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Limited experience in a laboratory or regulated environment preferred
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Basic understanding of laboratory techniques and aseptic practices preferred
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Strong attention to detail and ability to follow instructions
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Good written and verbal communication skills
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Ability to prioritize tasks and work as part of a team
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Comfortable working in cleanroom environments, including performing physical tasks such as climbing ladders when needed
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. 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.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.