Quality Control Supervisor at Lonza Inc. in Portsmouth, New Hampshire

Posted in Science about 15 hours ago.

Type: Full-Time





Job Description:

 

Today, Lonza is one of the world’s largest healthcare manufacturing organizations operating across five continents.

Join Lonza AG as a Quality Control Supervisor and lead a team responsible for testing and releasing raw materials, in-process, and final product drug lots! This opportunity reflects our dedication to delivering elite products and ensuring quality and patient safety!

Key responsibilities:


  • Coordinates and plans QC testing for ongoing operational needs, ensuring timely, high-quality results to meet Manufacturing demands.


  • Provides a safe work environment for the staff, ensuring safety procedures are strictly communicated and adhered to.


  • Builds, reviews, and approves QC documentation, and implements robust laboratory management systems.


  • Schedules and attends department and site-related meetings to assure delivery, adherence to quality systems, and improvement.


  • Ensures timely completion of all projects by ensuring task completion and presenting potential issues to collaborators.


  • Troubleshoots and resolves issues through team efforts, encouraging a cohesive team environment passionate about achieving company goals.


  • Leads OE initiatives, continuous improvements, and implementation of new processes and procedures to support site and corporate growth.


  • Recruits and guides team members, assists with regulatory and customer audits, and builds and implements CAPA plans.


Key requirements:


  • Proven experience in Quality Control within the life sciences or pharmaceutical industry.


  • Proven track record to recognize deviation from accepted practices and efficiently implement corrective actions.


  • Strong interpersonal and planning skills to ensure the detailed execution of QC testing.


  • Ability to handle non-routine assignments and problems of sophisticated technical scope.


  • Dedication to crafting a structured execution environment with a strong level of integrity.


  • Experience with cGMP and regulatory requirements, ensuring compliance and continuous improvement.


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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