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

Lonza • Houston, TX

291d

About The Position

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.

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.

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.

What This Job Offers

• Career Level: Mid Level
• Industry: Professional, Scientific, and Technical Services
• Education Level: Bachelor's degree