QC Analyst II - Cell Therapy

Lonza•Portsmouth, NH

9d•Onsite

About The Position

As a QC Analyst II on our Cell Therapy Analytical team, you are a vital link in the chain of patient care. You will perform high-precision testing—such as Flow Cytometry and Molecular assays—that confirms the safety and potency of personalized medicines. This role is designed for a detail-oriented scientist who is ready to take more ownership of laboratory operations and provide reliable, high-quality data in a fast-paced environment that bridges the gap between our day and night operations. 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.

Requirements

1–2 years of experience in a regulated lab environment (GMP/GLP).
Associate’s or Bachelor’s degree in a Scientific Discipline (Biology, Microbiology, Biochemistry, or related field) is required.
Familiarity with laboratory computer systems (LIMS) and a strong desire to master complex analytical instrumentation.
Ability to consistently work the 2nd Shift, 11:00 AM – 9:30 PM, Sunday-Wednesday Schedule. This shift requires a self-motivated individual who can maintain high energy and focus through the afternoon hours.
An uncompromising commitment to following Standard Operating Procedures (SOPs) and maintaining meticulous records.

Nice To Haves

Recent college graduates who have demonstrated exceptional technical aptitude in their academic labs and are eager to launch their careers in a fast-paced industrial setting.

Responsibilities

Perform complex analytical assays to support in-process, lot release, and stability testing. At the Level II stage, you will be expected to perform these tasks with increasing independence.
Maintain the highest standards of sterility when handling sensitive human biological samples to ensure 100% data integrity and prevent contamination.
Document results in real-time following Good Documentation Practices (GDP). You will participate in the initial review of data and help ensure the lab remains in a constant state of audit-readiness.
Identify and escalate results that deviate from expected ranges. You will assist senior analysts and supervisors in "root cause" investigations when technical variances occur.
Support the lifecycle of the lab by assisting with equipment qualifications, reagent preparation, and the maintenance of a safe, cGMP-compliant workspace.
Act as a critical communication bridge between day and night operations, ensuring seamless handovers to maintain production momentum.