This is a highly visible scientific leadership role for an experienced pathogen safety professional who can work independently, solve complex problems, and influence decisions across a cross-functional organization.

You will serve as the senior pathogen safety scientific representative for the assigned site, partnering with Operations, Quality, Regulatory, MS&T, and Global Pathogen Safety to assess and resolve complex scientific and operational matters.

The work is varied and may include evaluating deviations and changes, assessing emerging pathogen risks and potential product impact, supporting contamination control strategies, responding to regulatory requests, and providing scientific guidance on complex manufacturing and product-related issues.

You will operate with a high degree of independence while remaining connected to the broader Global Pathogen Safety organization and contributing to global scientific standards and best practices.

• Serve as the senior pathogen safety scientific expert and primary interface for the assigned site.
• Independently assess and resolve complex pathogen safety matters throughout the product lifecycle.
• Provide expertise for risk assessments, deviations, changes, product complaints, pharmacovigilance investigations, contamination control strategies, audits, inspections, and regulatory requests.
• Partner with Operations, Quality, Regulatory, MS&T, and other functions to provide scientific recommendations and drive resolution.
• Evaluate emerging pathogens and assess potential impact to products and operations.
• Influence decisions and drive alignment across functions and sites without direct authority.
• Contribute to global Pathogen Safety initiatives, standards, best practices, and knowledge sharing.
• Provide scientific coaching, technical guidance, and pathogen safety training.
• Support continuous improvement of pathogen safety processes, risk assessments, and tools.
• Ensure activities meet applicable regulatory requirements and internal quality standards

• Postgraduate degree, preferably PhD, in Virology, Biology, Microbiology, Immunology, or a related life sciences discipline.
• 5+ years of relevant biopharmaceutical industry experience, with significant experience in pathogen safety, viral safety, biologics manufacturing support, or a related discipline.
• Strong expertise in pathogen safety, including virus and prion safety.
• Demonstrated ability to independently lead complex scientific assessments and solve problems.
• Experience working cross-functionally in a matrix organization and influencing without direct authority.
• Strong stakeholder management and communication skills.
• Ability to communicate complex scientific concepts and recommendations to both technical and senior business audiences.
• Experience working across functions, cultures, and/or international locations is preferred.

Success in this role means becoming a trusted scientific authority for pathogen safety at the site. You will bring independent scientific judgment to complex situations, provide practical recommendations, influence cross-functional decisions, and serve as a strong connection between the local manufacturing site and the global Pathogen Safety organization.

This role offers the opportunity to take on a highly visible senior scientific position while remaining on a scientific career path. You will have significant autonomy, broad exposure across Operations, Quality, Regulatory and MS&T, and the opportunity to work on a wide variety of scientific and manufacturing challenges. You will also be part of a global Pathogen Safety network, giving you the opportunity to exchange expertise across international sites, contribute to global practices, and represent the organization at relevant scientific and industry forums.

Hybrid schedule with three days per week on site.

Ability to manage multiple priorities in a fast-paced, matrixed environment.

May occasionally require meetings outside standard business hours due to global collaboration.

Some travel to manufacturing/development sites, partners, meetings, or conferences may be required.

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