QC Analyst 2 (Environmental Monitoring) - Cell Therapy

Lonza•Portsmouth, NH

8d•Onsite

About The Position

The Quality Control (QC) Analyst 2 will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. They will also participate in quality testing for ongoing customer stability studies and provide on-time, high quality results to meet Lonza’s manufacturing demands.

Requirements

Bachelor's or Associate's Degree preferably in Microbiology, Biochemistry, or related science discipline.
2-4 year’s of GMP industry experience; aseptic experience is preferred.
Use of Microsoft Suites (Word, Excel, PowerPoint) and Laboratory computer systems.
Experience using GMP Quality Systems such as: TrackWise, LIMS preferred.
Perform assigned, complex and/or varied tasks.
Exercises judgment within defined procedures and practices to determine appropriate action.
Self-motivated team player.

Responsibilities

Run test samples for in-process, lot release and stability studies.
Writing quality records (Deviations, CAPA, Change Control) and test methods.
Applies job skills and company's policies and procedures to complete a variety of tasks.
Reviewing assays.
Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required.
Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.
Apply Data Integrity principles in all aspects of work, in compliance with Lonza DI policies, guidelines and procedures.