Sterile Manufacturing Value Stream Lead

Viatris; Inverin; In loco; EUR 90.000 - 130.000; Tempo pieno

Vantaggi offerti da questo lavoro

Competitive salary

Inclusive environment

Descrizione del lavoro

Mylan Teoranta Viatris, based in Ireland, is seeking a manufacturing leader to drive the development, scale-up and validation of a sterile cartridge filling line. You will ensure readiness for PPQ and commercial production, while supporting risk management and regulatory readiness.

The role requires extensive experience in sterile GMP environments, project leadership and a track record of delivering process improvements.

Competenze

• Bachelor's degree in engineering or related field with sterile manufacturing experience.
• GMP pharmaceutical or medical device manufacturing experience required.
• Experience leading production teams and developing operators.
• Experience supporting equipment commissioning and qualification.

Mansioni

• Lead manufacturing activities for development, scale-up, process validation and commercial launch of a sterile cartridge filling line.
• Ensure readiness for engineering runs, PPQ batches and commercial production.
• Participate in project governance meetings and provide updates on manufacturing risks, resources and timelines.
• Support equipment FAT, SAT, commissioning and qualification activities.
• Build and develop a manufacturing team capable of supporting commercial operations.

Conoscenze

GMP experience

Sterile manufacturing

Leadership / supervisory experience

Process validation

Aseptic processing knowledge

Formazione

Bachelor's Degree in Engineering, Science, Pharmaceutical Technology, Biotechnology or related discipline

Descrizione del lavoro

Mylan Teoranta Viatris, based in Ireland, is seeking a manufacturing leader to drive the development, scale-up and validation of a sterile cartridge filling line. You will ensure readiness for PPQ and commercial production, while supporting risk management and regulatory readiness.

The role requires extensive experience in sterile GMP environments, project leadership and a track record of delivering process improvements.