Quality Control (QC Analyst)
United States, Portsmouth (New Hampshire)

Quality Control (QC) Analyst - Release Testing

Location: Portsmouth, NH

Be the guardian of processes that make products safe and effective, and make a meaningful difference from day one. As a Quality Control Analyst at Lonza, you will have the opportunity to support the production of in-process and final product drug lots that enable a healthier world.

Join a team-based environment that embraces inclusivity and ethics, where you can be challenged to work on problems that require a high level of attention to detail. At our global hub in Portsmouth, NH, you will be able to apply your ability to recognize deviations from accepted practice, and bring high standards to healthcare innovation.

Check out more about what a life at Lonza in Portsmouth, NH could look like for you. 

Today, Lonza is a global leader in life sciences operating across five 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 you to be part of.

Shift Schedule: 10 hours shift from 11am to 9.30pm on either of the below rotations:

  • Sunday - Wednesday

  • Wednesday - Sunday

Shift differential are included

What you’ll get:

  • A strong and supportive team culture

  • An agile career and stimulating work

  • Compensation programs that recognize high performance

  • A variety of benefits, dependant on role and location

What you’ll do:

  • Apply company policies and procedures

  • Run test samples for in-process, lot release and stability studies

  • Provide on-time and high quality results to meet manufacturing demands

  • Review assays and writing quality records (Deviations, CAPA, Change Control) and test methods

  • Recognize deviations from accepted practices

  • Performs other duties, as assigned

What we’re looking for:

  • Bachelor's or Associate Degree preferably in Microbiology, Biochemistry, or related science discipline

  • Two to four 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: TrackWise, 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.

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.

Reference: R63388
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