Sterile Drug Product Associate — Start-Up GMP Innovator

Bristol-Myers Squibb Co; Cruiserath; Presencial; EUR 55.000 - 75.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

27 days annual leave

Pension contribution

Family medical allowance

Life assurance

On-site gym

Descripción de la vacante

Bristol Myers Squibb is seeking a Drug Product Associate for sterile manufacturing operations in Ireland. You will support formulation, filling, lyophilization, Capping, visual inspection and packaging processes, contributing to Start-up and ongoing manufacturing readiness.

In this role you’ll assist with commissioning, qualification and validation activities, participate in process improvements, and work with cross-functional teams to ensure compliance, quality and timely delivery of products

Formación

• Experience in high-speed manufacturing and regulated environments.
• Desirable background in sterile drug product manufacturing.
• Strong troubleshooting and process improvement skills.

Responsabilidades

• Support execution of Formulation, Filling, Lyophilization, Capping, Visual Inspection and Packaging.
• Assist with commissioning, qualification and validation during start-up.
• Collaborate with cross-functional teams to enable project design and SDP facility validation.
• Support capital transfers, tech transfers and operational readiness activities.
• Contribute to training delivery for SDP team on day-to-day operations.
• Participate in investigations and optimization using lean principles.

Conocimientos

High-speed manufacturing

Regulated environment

Troubleshooting

Lean/Continuous improvement

Adaptability

Educación

Science/Engineering degree

Herramientas

Process automation systems

Descripción del empleo

Bristol Myers Squibb is seeking a Drug Product Associate for sterile manufacturing operations in Ireland. You will support formulation, filling, lyophilization, Capping, visual inspection and packaging processes, contributing to Start-up and ongoing manufacturing readiness.

In this role you’ll assist with commissioning, qualification and validation activities, participate in process improvements, and work with cross-functional teams to ensure compliance, quality and timely delivery of products