QC Analyst I – Microbiology (Cell Therapy)
Lonza
This listing was originally posted on Lonza's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
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QC Analyst I – Microbiology (Cell Therapy)
Location: Portsmouth, NH, USA.
Schedule: 1st Shift, Wednesday - Saturday, 7:00 am – 5:30 pm.
We are seeking a motivated individual to join our Microbial Control team in Portsmouth, NH, as a QC Analyst I. This entry-level role is a foundational step in our Cell Therapy asset, where you will ensure the safety of personalized, life-saving therapies through rigorous environmental monitoring and laboratory testing.
What will you get?
An agile career and dynamic working culture
An inclusive and ethical workplace
Comprehensive Training: Master a dual skillset in both technical "bench" microbiology and in-suite environmental monitoring.
Work-Life Balance: A consistent 4-day work week providing three days off to recharge.
Compensation programs that recognize high performance
Medical, dental and vision insurance, as well as PTO and more
Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.
What you’ll do:
Microbial Testing: Perform routine test samples for In-Process, Lot Release, and Stability studies to support manufacturing demands.
Facility Support: Execute Utility and HVAC monitoring and sampling throughout the facility to ensure a controlled manufacturing environment.
Aseptic Excellence: Perform work within classified manufacturing suites, maintaining strict aseptic standards and gowning requirements.
Data Integrity: Apply Data Integrity principles in all aspects of work, following Lonza policies to ensure 100% compliance with cGMP standards.
Lab Systems: Utilize Microsoft Office and specialized laboratory computer systems (LIMS) to record and track critical results.
Problem Recognition: Learn to recognize and escalate deviations from accepted practices, helping the team maintain total process control.
Collaborative Quality: Work as an active member of the team to provide on-time, high-quality results in a fast-paced environment.
What we’re looking for:
Education: Associate’s or Bachelor’s Degree in Microbiology, Biochemistry, or a related Science field is preferred; High School Diploma or equivalent is required.
Experience: This is an entry-level (0–4 years) role; prior experience in a GMP or laboratory environment is a plus but not required.
Technical Aptitude: Ability to comprehend and follow detailed Standard Operating Procedures (SOPs) and a strong desire to learn complex laboratory instrumentation.
Physical Requirements: Ability to stand/walk for portions of the shift and comfort with sterile gowning procedures. Must be able to occasionally lift up to 50 lbs.
Core Skills: High attention to detail, a positive attitude, and a deep commitment to safety and quality.
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.
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