QA Specialist III (Sun - Thur 3PM-12AM)

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Houston, TX, USA
In-Office
Pharmaceutical
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization.
The Role

 

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 to be part of.

Join Lonza AG as a QA Specialist III in our world-class manufacturing team in Houston, TX! This outstanding opportunity allows you to support our mission of delivering flawless quality in life sciences. At Lonza, we are ambitious and driven to strictly adhere to the highest standards, ensuring our products make a positive impact on people’s lives.

Key responsibilities:

  • Perform the Quality Assurance review of GMP documents, including master documents, completed documents, and quality-controlled documents.

  • Conduct QA walkthroughs and collaborate closely with manufacturing and support groups to identify and resolve any issues.

  • Support manufacturing operations and related groups to ensure quality requirements are met.

  • Use problem-solving tools to support investigations and implement corrective actions as needed.

  • Review and manage GMP documents from various departments, including QC, manufacturing, and material management.

  • Track quality records and ensure overall cGMP compliance through QA on the floor execution.

Key requirements:

  • Proven experience in Quality Assurance within a manufacturing environment.

  • Strong understanding of GMP (Good Manufacturing Practice) guidelines.

  • Outstanding problem-solving skills and the ability to determine and implement corrective actions.

  • Ability to work collaboratively with cross-functional teams to achieve ambitious goals.

  • Meticulous attention to detail and a dedication to maintaining the highest quality standards.

  • Excellent communication skills and the ability to lead QA initiatives successfully.

  • Bachelor's degree in Life Sciences or Engineering.

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. 

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The Company
HQ: Basel
0 Employees
Year Founded: 1897

What We Do

At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.

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