QC Analyst II - Analytical (Second Shift)

Lonza•Portsmouth, NH

7d•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. What You’ll Get Advanced Technical Mastery: Refine your expertise in cutting-edge analytical techniques (Flow Cytometry, ELISA, qPCR) used in the release of world-class cell-based therapies. Direct Patient Connection: Your work is the final verification that a custom treatment is safe for the specific patient waiting for it. Work-Life Balance: Our 4x10 schedule provides three consistent days off per week (Sunday, Monday, Tuesday), allowing you to avoid the standard 9-to-5 grind and enjoy mid-week flexibility. Full Lonza Benefits: Medical, dental, vision, 401(k), and performance-based incentives. lonza.com/careers/benefits . What You’ll Do Analytical Execution: 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. Aseptic Excellence: Maintain the highest standards of sterility when handling sensitive human biological samples to ensure 100% data integrity and prevent contamination. Data & Compliance: 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. Problem Solving & Investigations: Identify and escalate results that deviate from expected ranges. You will assist senior analysts and supervisors in "root cause" investigations when technical variances occur. Lab Stewardship: Support the lifecycle of the lab by assisting with equipment qualifications, reagent preparation, and the maintenance of a safe, cGMP-compliant workspace. Shift Synergy: Act as a critical communication bridge between day and night operations, ensuring seamless handovers to maintain production momentum.

Requirements

Experience: We are looking for candidates with 1–2 years of experience in a regulated lab environment (GMP/GLP).
The "New Grad" Exception: We are highly open to 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.
Education: Associate’s or Bachelor’s degree in a Scientific Discipline (Biology, Microbiology, Biochemistry, or related field) is required.
Technical Aptitude: Familiarity with laboratory computer systems (LIMS) and a strong desire to master complex analytical instrumentation.
The 2nd Shift Mindset: Ability to consistently work the 11:00 AM – 9:30 PM schedule. This shift requires a self-motivated individual who can maintain high energy and focus through the afternoon and evening hours.
Attention to Detail: An uncompromising commitment to following Standard Operating Procedures (SOPs) and maintaining meticulous records.

Responsibilities

Analytical Execution: Perform complex analytical assays to support in-process, lot release, and stability testing.
Aseptic Excellence: Maintain the highest standards of sterility when handling sensitive human biological samples to ensure 100% data integrity and prevent contamination.
Data & Compliance: 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.
Problem Solving & Investigations: Identify and escalate results that deviate from expected ranges. You will assist senior analysts and supervisors in "root cause" investigations when technical variances occur.
Lab Stewardship: Support the lifecycle of the lab by assisting with equipment qualifications, reagent preparation, and the maintenance of a safe, cGMP-compliant workspace.
Shift Synergy: Act as a critical communication bridge between day and night operations, ensuring seamless handovers to maintain production momentum.