Lonza
QC Analyst II-Microbial Control
United States · Work style not stated · Full time
Apply on the employer’s site ↗See how well you match this job
You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.
About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerLonza
- LocationUnited States
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
JobTitle: Quality Control Analyst II – Microbial Control (Night)
Location: Portsmouth, NH, (On-site)
As a QC Analyst II in Microbial Control at our Portsmouth site, you will support the testing of in-process and final product samples to ensure the safety and quality of drug products. You will perform microbiological testing, support environmental and utility monitoring, and deliver accurate results to meet manufacturing timelines. 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 6:00 AM.
What you will get
- Competitive pay and performance-based compensation
- Medical, dental, and vision insurance
- A supportive and inclusive work environment
- Opportunities for career growth and development
- Hands-on training and skill-building
- A collaborative and team-focused laboratory environment
Show full description
What you will do
- 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
- Ensure compliance with cGMP, GDP, and data integrity requirements in all tasks
- Participate in routine lab activities, including sample handling and documentation
What we are looking for
- Associate’s degree in Microbiology, Biochemistry, or a related science field
- Experience in a GMP or regulated laboratory environment preferred
- Ability to interpret data and identify trends or deviations
- Strong written and verbal communication skills
- Attention to detail and strong organizational skills
- Prior laboratory experience, familiar with aseptic techniques and strong documentation practices, preferred
- 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.
Check your resume against this job Free, no sign-up. Nothing you paste is stored.
Staying safe while you apply
- Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
- Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
- Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.
Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.
Preparing for this role with ROLIVA
- Check the fit.
Compare the requirements with the experience you have confirmed, including gaps.
- Prepare honestly.
Build interview stories and application drafts from your own evidence.
- Keep track.
Save the role and record your own application status and follow-ups.
At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked