executivekarriere
Zurück zu den Treffern

Director of Sterile Manufacturing Technical Capability & Training

Anzeige auf Englisch

BeschäftigungVollzeit
Gehalt120.000–160.000 € brutto/Jahr
HomeofficeKeine Angabe

Director of Sterile Manufacturing Technical Capability & TrainingBewerben:

United Kingdom Remote Office: Germany Remote Office: Ireland Remote Office: France Remote Office: Vollzeit: Heute ausgeschrieben: R5675638Generics [U.K.] Ltd. Viatris ist ein globales Gesundheitsunternehmen, das einzigartig positioniert ist, die traditionelle Kluft zwischen Generika und Marken zu überbrücken und das Beste von beiden zu verbinden, um weltweit umfassendere Gesundheitsbedürfnisse zu adressieren. Mit der Mission, Menschen weltweit zu befähigen, in jeder Lebensphase gesünder zu leben, bieten wir Zugang in großem Maßstab, liefern derzeit jährlich etwa 1 Milliarde Patienten weltweit hochwertige Medikamente und berühren alle Lebensmomente – von der Geburt bis zum Lebensende, von akuten Erkrankungen bis hin zu chronischen Krankheiten. Wir wurden auf zahlreiche Auszeichnungslisten aufgenommen, die die Wirkung zeigen, die wir erzielen.

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. Purpose of Role: We are seeking an experienced leader to drive the development of technical capability across our global sterile manufacturing network.

As Director of Sterile Manufacturing Technical Capability & Training, you will lead the design and implementation of a global training and competency strategy that strengthens expertise in sterile manufacturing, sterility assurance and contamination control, while supporting regulatory compliance, operational excellence and inspection readiness. The Role & What You Will Be Doing Every day, we rise to the challenge to make a difference and here’s how the Director of Sterile Manufacturing Technical Capability & Training role will make an impact:

  • Develop and execute a global technical training and capability strategy for sterile manufacturing and contamination control.
  • Build role-based learning pathways, competency frameworks and qualification programmes across Manufacturing, Quality, Engineering, Microbiology and Validation.
  • Lead the creation and delivery of engaging technical training, workshops and capability-building initiatives.
  • Partner with global and site SMEs to translate complex scientific, engineering and regulatory concepts into practical learning.
  • Establish a network of site Technical Training SPOCs to drive consistent capability development across the organisation.
  • Support inspection readiness by embedding regulatory expectations and organisational learning into training programmes.
  • Use audit findings, investigation trends and performance data to identify capability gaps and drive continuous improvement.
  • Promote best practice sharing and harmonisation across a global manufacturing network.
  • Explore innovative learning solutions, including digital and immersive technologies, to enhance technical capability development. About Your Skills & Experience For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:
  • Bachelor's degree in Microbiology, Pharmaceutical Sciences, Engineering, Biotechnology or a related discipline; advanced qualifications are desirable.
  • Significant experience in sterile or aseptic pharmaceutical manufacturing, Sterility Assurance, Microbiology, Engineering or a related technical field.
  • Deep knowledge of contamination control, aseptic processing, sterile manufacturing and global GMP requirements, including EU GMP Annex 1.
  • Proven experience developing and delivering technical training, competency programmes or capability-building initiatives.
  • Strong ability to communicate complex technical concepts and influence stakeholders across a global organisation.
  • Recognised technical credibility with excellent coaching, facilitation and mentoring skills.
  • Experience supporting regulatory inspections, remediation programmes and multi-site manufacturing environments is highly desirable.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, we still encourage you to apply. You may just be the right candidate for this or other roles. Why 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. You will also have the opportunity to access excellent career progression opportunities and work-life balance initiatives.

Arbeitgeber

Mehr Stellen finden

Ähnliche Stellen bei anderen Arbeitgebern

Arbeitgeber mit ähnlichen Stellen

Verwandte Fachgebiete