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Lonza

Quality Control (QC Analyst)

Lonza, Portsmouth, New Hampshire, United States, 03804

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locations

US - Portsmouth, NH

time type

Full time

posted on

Posted 4 Days Ago

job requisition id

R63388

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, theres 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 thats 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 youll 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 youll 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 were 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, Lonzas 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.