Senior Supervisor, Advanced Therapies Pilot Plant Scale-Up

8852-Janssen Vaccines & Prevention B.V. Legal Entity; Netherlands; On-site; EUR 64,000 - 103,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Well-being reimbursement

Insurance plans

Job summary

Johnson & Johnson Leiden is seeking a Senior Supervisor for the Advanced Therapies Pilot Plant (ATP) operations team. You will lead scale-up production activities and build a capable, high-performance team to deliver GMP material for clinical trials.

Responsibilities include managing project plans, coaching staff, coordinating with process development, and ensuring timely communication of issues to senior management. English in pharma context is essential; strong leadership is required.

Qualifications

• Education: MSc or equivalent with 5-10 years of Pharma/biotech industry experience.
• Experience in GMP operations across multiple areas is required.
• Experience in process development of large molecule manufacturing is a benefit.
• Strong team building and project management skills.
• Knowledge of lean manufacturing tools (e.g. green belt) is advantageous.

Responsibilities

• Establish the new scale-up production capability with the project team to meet ATP needs.
• Build an operations team with required skills and training.
• Supervise contributors and coach junior colleagues in techniques and responsibilities.
• Lead ATP processes and assignments, including introducing new products into the plant.
• Ensure timely communication of issues to senior management.

Skills

Agile Manufacturing

Leadership

Project management

Data analysis

GMP

Process optimization

CMC

Operational Excellence

Developing Others

Communication

Education

MSc or equivalent

Tools

Lean manufacturing tools

Job description

Johnson & Johnson Leiden is seeking a Senior Supervisor for the Advanced Therapies Pilot Plant (ATP) operations team. You will lead scale-up production activities and build a capable, high-performance team to deliver GMP material for clinical trials.

Responsibilities include managing project plans, coaching staff, coordinating with process development, and ensuring timely communication of issues to senior management. English in pharma context is essential; strong leadership is required.