Senior Project Manager R&D PMO at Hollister Incorporated in Ballina, MY, IE, F26 F3X5

Job description

• This Senior role leads cross-functional teams in the development and commercialization of new products within the New Product and Process Development (NPPD) process. The Senior Project Manager will be responsible for planning, executing, and delivering integrated business cases, ensuring alignment with organizational strategy.
• They will build strong relationships with senior stakeholders, support a high-performance culture, and, at Senior level, provide mentorship and guidance to other project managers. Collectively, these roles are accountable for delivering high-quality, market-aligned outcomes and driving continuous improvement across the product development lifecycle.

Responsibilities

• • Lead cross-functional core teams through all phases of product development and commercialization.
• • Develop integrated business and commercialization plans supporting global product launch strategies.
• • Plan, schedule, and manage project activities to meet objectives and compliance requirements.
• • Track and manage project budgets, schedules, and ROI targets.
• • Build strong partnerships with functional leaders and key stakeholders.
• • Promote a culture of innovation, accountability, and results.
• • Provide strategic guidance, structured thinking, and clear delegation to project teams.
• • Mentor and coach project managers, core team leaders, and team members.
• • Drive process adherence, best‑practice project management, and continuous improvement initiatives.
• • Facilitate effective decision making using sound judgment and scenario evaluation.
• • Provide input to annual planning regarding resource needs for development initiatives.

Requirements

• Bachelor’s Degree with 8-12 years of related experience
• • Technical Bachelor’s degree required.
• • 8–10 years of experience managing complex product development projects, preferably in medical devices.
• • Minimum 5 years leading projects or cross‑functional teams.
• • Experience with product development, commercialization, and enterprise‑level process initiatives.
• • Knowledge of regulatory environments, including 21 CFR, QSR 830, ISO 13485, and ISO 14971.
• • Master’s degree (e.g., MS, MBA, Engineering) preferred.
• • PMP certification preferred.
• • Experience in risk management, quality systems, and enterprise‑wide process improvement.
• • Experience in matrixed environments with multiple stakeholder groups.

Skills

Required

• Project management
• Cross-functional team leadership
• Strategic planning
• Budget management
• Stakeholder management
• Process improvement
• Risk management
• Quality systems
• Decision-making
• Resource allocation
• Time management
• Mentoring and coaching

Preferred

• PMP certification
• Experience in medical devices
• Experience in matrixed environments