What are the responsibilities and job description for the GMP Production Manager position at client.lonza.display?
GMP Manufacturing Supervisor - Nights
Lonza, a global leader in life sciences, operates across three continents. Our scientific solutions rely on talented people working together to devise ideas that help businesses improve lives. In return, we empower our people to own their careers and make a meaningful difference.
Key Accountabilities and Duties:
- Coordinate and support production activities for Cell and Gene processes at LPO, including pilot runs through GMP manufacturing.
- Facilitate the set up and execution of manufacturing procedures to comply with quality systems and ensure timely delivery of clinical & commercial material.
- Develop the manufacturing team to meet business needs and personal career goals, while maintaining clean and organized manufacturing areas.
- Provide oversight and support for Technical Transfer activities, including equipment and material requirements, process execution, and optimization.
Requirements:
- Experience in biological GMP manufacturing operations, particularly in Fermentation, Purification, Drug Product Filling, and Freezing processes.
- Leadership experience in organizational change, staff hiring, and training.
- Quality responsibility: adherence to cGMPs and notification of regulatory inspections, serious GMP deficiencies, process deviations, product defects, and related actions.
About Lonza:
Lonza is an equal opportunity employer. We respect and protect our people and environment, and strive to achieve business results ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences.
Estimated Salary: $80,000 - $120,000 per year.
Salary : $80,000 - $120,000
