GMP Manufacturing Supervisor(Days)

Today, Lonza is a global leader in life sciences operating across three 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.

Are you prepared to accept a challenging position with a global leader in life sciences? Lonza AG is looking for a highly motivated GMP Supervisor to join our outstanding team. This role provides an outstanding opportunity to contribute to innovative projects and progress your career in a world-class setting. Join us in our mission to enhance lives through science!

Key Accountabilities and Duties:

• Coordinate and support the execution of production activities for all Cell and Gene processes, ensuring flawless compliance with ET & site quality systems.
• Develop the manufacturing team to meet both business needs and personal career goals.
• Support the timely, in-full delivery of clinical & commercial material.
• Coordinate EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management, and EM strategies.
• Maintain manufacturing areas to the highest cleanliness and 6S standards.
• Support technology transfer activities and ensure timely achievement of goals.

Supervision Received

The incumbent establishes methods and procedures for attaining specific goals and objectives and receives mentorship in terms of broad goals. Only the final results of work are typically reviewed.

Essential Job Functions

The GMP Supervisor will help Lonza grow in life sciences by ensuring manufacturing success.

Key responsibilities:

• Coordinate and support production activities for Cell and Gene processes.
• Develop and lead the manufacturing team.
• Ensure compliance with quality systems and EHS strategies.
• Coordinate technology transfer activities and achievement execution.
• Maintain high standards of cleanliness and operational efficiency.

Key requirements:

• BS degree preferred; significant experience may be considered in lieu of degree.
• Minimum 5 years related experience with a degree, or 8 years without.
• Proven experience in biological GMP manufacturing operations.
• Strong leadership and team development skills.
• Ability to coordinate complex projects and ensure timely delivery.

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.