Director, Injectable Device Programs Lead

Viatris; Dublin; On-site; EUR 110,000 - 150,000; Full time

Benefits offered by this job

Health insurance

Bonus scheme

Pension

Diversity & Inclusion

Work-life balance

Job summary

Viatris seeks a Director, Device Project Management to lead cross-functional teams in the development and transfer of injectable drug-device technologies (autoinjector, prefilled pen, PFS, vial-kit).

You will drive strategic direction, manage milestones, risks, budgets and resources, mentor program leads, and collaborate with global device development teams to ensure timely delivery of robust device CMC programs for global registrations.

Qualifications

• Degree in a pharmaceutical science or engineering, or equivalent.
• MSc, PhD or MBA is desirable.
• 10+ years experience in medical device or combination product engineering, with at least 5 in a leadership role.
• Proven track record of managing programs and leading complex cross functional program teams.
• Experience of leading a drug delivery device programme through development to product scale-up and launch.

Responsibilities

• Provide technical program management leadership during the development and transfer of injectables products.
• Develop and execute strategic workplan for the Injectables Portfolio.
• Drive progress of allocated programs, developing a holistic summary of key milestones, program risks, budget and resource.
• Lead and mentor Program Leads on the development of Combination Products.
• Deliver technical project plans linked goals on time and within resource and expenditure budgets.

Skills

Program management

Cross-functional leadership

Stakeholder management

Communication skills

Leadership

Education

Bachelor's degree in pharmaceutical science or engineering

MSc/PhD/MBA desirable

Tools

MSP

Job description

Viatris seeks a Director, Device Project Management to lead cross-functional teams in the development and transfer of injectable drug-device technologies (autoinjector, prefilled pen, PFS, vial-kit).

You will drive strategic direction, manage milestones, risks, budgets and resources, mentor program leads, and collaborate with global device development teams to ensure timely delivery of robust device CMC programs for global registrations.