Ensures right first time, inspection-ready User Interface deliverables.
Maintains close partnerships with relevant global business owners through collaborative engagement with key stakeholders and establishing advocates in stakeholder teams.
Oversees external vendors and study execution, ensuring methodological rigor, compliance, and timely delivery of Human Factors evidence.
About You
Degree in Pharmaceutical Science, Medical Device/Product Design, or equivalent.
Extensive experience in Pharmaceutical Development, Human Factors Engineering, or Medical Device/Combination Product Engineering, including several years in a leadership role.
Proven track record leading development strategy and program execution.
Knowledge of drug delivery technologies — e.g. pen injectors, autoinjectors, vial kits, inhaler technologies, and prefilled syringes.
Detailed knowledge of key industry standards, including EU MDR, ISO 13485, ISO 14971, ISO 62366, and 21 CFR Part 820.
MSc, PhD, or MBA, and experience with both NCE and Generic product development are a plus.
At Viatris, we're building a truly diverse, inclusive, and authentic workplace. If you're excited about this role but your experience doesn't fully align with every requirement, we still encourage you to apply.
Benefits at Viatris
Excellent career progression opportunities
Work-life balance initiatives
Bonus scheme
Health insurance
Pension
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.
Viatris is an Equal Opportunity Employer.