QC Analyst I
This is a fully site-based role located in Portsmouth, NH supporting critical Quality Control operations in microbiological testing and environmental monitoring. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will get:
Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.
What you will do:
Directly contribute to patient safety by ensuring high-quality microbiological compliance in the release of life-saving pharmaceutical products.
Collaborate with cross-functional teams and key stakeholders across the Quality Control and Manufacturing departments.
Perform environmental monitoring and sampling for Utility and HVAC systems throughout the Portsmouth facility.
Conduct routine testing on in-process samples, final product lot release, and ongoing customer stability studies.
Maintain strict compliance with Data Integrity principles and cGMP regulations across all documentation and laboratory workflows.
Utilize laboratory computer systems and standard office software to record, process, and review testing data.
Recognize deviations from accepted practice and assist in resolving technical problems of moderate scope.
What we are looking for:
High School Diploma required; Associate’s or Bachelor’s degree in Microbiology, Biochemistry, or a related scientific field preferred.
0–4 years of experience in Quality Control or a laboratory environment (entry-level candidates are encouraged to apply).
Practical familiarity with environmental monitoring, utility/HVAC sampling, or microbiology test methods is ideal.
Understanding of cGMP compliance and Data Integrity principles in a regulated environment.
Proficiency in standard office tools (Word, Excel, PowerPoint, Teams) and familiarity with laboratory software systems.
Strong problem-solving, communication, and organizational skills with strict attention to detail and accuracy.
Ability to work effectively within a team structure and adapt flexibly to daily production demands.
About Lonza
At Lonza, their people are their greatest strength. With 30+ sites across five continents, their globally connected teams work together every day to manufacture the medicines of tomorrow. Their core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who they are and how they work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work they want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, they value diversity and are committed to creating an inclusive environment.
As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.
Ready to play your part in shaping the future of life sciences? Apply now.