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Director of Sterile Manufacturing Technical Capability & Training

Job in Boise, Ada County, Idaho, 83701, USA
Listing for: Viatris
Full Time, Apprenticeship/Internship position Listed on 2026-11-13
Job specializations:
Salary/Wage Range or Industry Benchmark: 159000 - 239000 USD Yearly USD 159000.00 239000.00 YEAR

Job Description & How to Apply Below

Location:

France;
Germany;
Ireland;
United Kingdom

Generics [U.K.] Ltd.

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.

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…
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