QC Analyst III-Microbial Control (Biotech)
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of!
Join Lonza, a global leader in life sciences, and be part of a team that drives innovation and excellence. As a QC Analyst in Microbial Control in New Hampshire, USA, you will play a vital role in ensuring the quality of our products. This position offers the opportunity to work in a dynamic environment where your contributions will help us compete at a world-class level and make a meaningful difference!
**The schedule for this position is Monday - Friday from 7:00 am - 3:30 pm**
Key responsibilities:
Conducting microbial control tests for In-Process, Lot Release, and Stability studies with flawless execution
Supporting Utility and HVAC monitoring and sampling throughout our brand new facility
Reviewing and analyzing assay results to ensure accuracy and compliance
Training new team members to ensure they meet our exceptionally high standards
Writing quality records, including deviations, CAPAs, change control, and test methods
Leading projects such as method transfers, new instrument implementation, and method qualifications
Applying Microsoft Suites (Word, Excel, PowerPoint) and laboratory computer systems efficiently
Applying GMP Quality Systems such as TrackWise and LIMS when necessary
Recognizing deviations from accepted practices and determining appropriate actions
Applying Data Integrity principles rigorously in all aspects of work, in compliance with Lonza's policies
Key requirements:
Associate's Degree or equivalent experience required; Bachelor's Degree in Microbiology, Biochemistry, or related science field preferred
3+ years of proven experience, preferably in a cGMP environment
Proficient use of Microsoft Suites (Word, Excel, PowerPoint)
Familiarity with GMP Quality Systems such as TrackWise and LIMS is advantageous
Strong data interpretation skills with a focus on attention to detail
Strong prioritization and problem-solving skills to figure out best course of action
Capability to interpret and carry out instructions with precision
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.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
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.
