QC Analyst Environmental Monitoring Nights

United States, Portsmouth (New Hampshire)

Posting an opportunity with Lonza. The Quality Control (QC) Analyst 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.

• Running test samples for in-process, lot release and stability studies.
• Reviewing assays.
• Writing quality records (Deviations, CAPA, Change Control) and test methods.
• Performs other duties as assigned.
• 10 Hour Night Shifts Either – Wednesday to Saturday, or Sunday to Wednesday, with schedules 8:00 am to 6:30 pm or 8:00 am to 5:00 pm.

• Bachelor's or Associate's Degree preferably in Microbiology, Biochemistry, or related science discipline.
• 2-4 years industry experience preferably in a cGMP environment.
• Use of Microsoft Suites (Word, Excel, PowerPoint).
• Use of Laboratory computer systems.
• Experience using GMP Quality Systems such as:
  Track Wise, LIMS preferred.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Reference: R72892