Value Stream Manager - Cartridge Filling

Viatris; Inverin; Presencial; EUR 90.000 - 130.000; Tempo integral

Benefícios oferecidos por esta vaga

Competitive salary

Inclusive environment

Resumo da vaga

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.

Qualificações

• 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.

Responsabilidades

• 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.

Conhecimentos

GMP experience

Sterile manufacturing

Leadership / supervisory experience

Process validation

Aseptic processing knowledge

Formação

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

Descrição da vaga

Mylan Teoranta Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases.

We have been included on number of award lists that demonstrate the impact we are making.

Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.

For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world.

The Role & What You Will Be Doing

• Lead manufacturing activities associated with development, scale-up, process validation and commercial launch of a sterile cartridge filling line.
• Ensure manufacturing readiness for engineering runs, process performance qualification (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.
• Provide manufacturing expertise during process design and optimization phases.
• Contribute to risk assessments including FMEA and quality risk management activities.
• Drive execution of project deliverables in alignment with overall program objectives.
• Support regulatory inspections and customer audits relating to the project.
• Build, recruit and develop a manufacturing team capable of supporting commercial operations.
• Ensure compliance with GMP, aseptic processing standards and site quality systems.
• Promote a strong quality culture and right-first-time manufacturing principles.
• Ensure audit readiness across all operational areas.
• Review manufacturing documentation for accuracy and compliance.

About Your Skills & Experience

• Bachelor's Degree in Engineering, Science, Pharmaceutical Technology, Biotechnology or related discipline.
• Equivalent combination of education th a significant sterile manufacturing experience may be considered.
• Proven experience in GMP pharmaceutical or medical device manufacturing.
• Proven experience in a supervisory or leadership position.
• Experience in sterile manufacturing and aseptic processing environments.
• Experience supporting new product introductions, technology transfers or commercialization projects.
• Experience managing production teams and developing operators.
• Track record of delivering operational improvements and performance results.
• Experience supporting equipment commissioning and qualification.
• Knowledge of Annex 1 requirements and aseptic manufacturing practices preferrable.

At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't fully align with every requirement.

You may just be the right candidate for this or other roles.

Benefits at Viatris

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Some of our benefits include the following on top of a competitive salary:

• Excellent care