What are the responsibilities and job description for the Biotechnology Production Manager position at client.lonza.display?
Job Description
We are seeking a highly skilled GMP Manufacturing Supervisor to join our team at Lonza. In this role, you will be responsible for coordinating and supporting the execution of production activities for all Cell and Gene processes.
The successful candidate will have a strong understanding of biological GMP manufacturing operations, including Fermentation, Purification, Drug Product Filling and Freezing processes. They will also have experience in Autologous / cross training environments requiring innovative resourcing solutions.
Key responsibilities include:
- Coordinating and supporting the execution of production activities for all Cell and Gene processes
- Facilitating the set up and execution of manufacturing procedures to comply with ET & site quality systems
- Developing the manufacturing team to meet business needs and personal career goals
Quality Responsibility
Adherence to cGMPs is required at all times during the manufacture of APIs. All personnel own the quality of what they deliver and are responsible for notifying responsible management in a timely manner of regulatory inspections, serious GMP deficiencies, process deviations, product defects and related actions.
Education and Experience
A minimum of 5 years related experience with a degree or 8 years without a degree is required. The ideal candidate will have a BS degree and relevant experience in biological GMP manufacturing operations.