
Project Mgr, PMO
- Marsa, Malta Island
- Permanent
- Full-time
- Provide business and technical leadership for a significant program within the Infusion Therapies and Technologies (ITT). The ITT business is a core growth area providing infusion pumps, intravenous drugs, and administration and pharmacy preparation devices.
- Lead cross functional scientific and technical teams in all aspects of project initiation, planning, execution, monitoring and closure for a compliance program.
- Provide leadership within the ITT business and manage stakeholder expectations with regard to deliverables during the program
- Lead teams in timely resolution of problems, including development of technical solutions, project plans, resourcing plans and budgets
- Develop core team and project management capabilities across the organization.
- Comfortable communicating with senior leaders inside and outside the business unit.
- Work within the guidelines of project management, standard performance metrics, and regulatory guidelines to apply best practice Project Management skills, methodologies and standards (such as PMBOK).
- Establish, track and communicate project risks
- Manage all financial aspects of assigned projects, from initiation through close, which may include capital expenditures, functional expenses, and program positioning.
- Bachelor’s Degree - Life sciences, chemical engineering or biotech disciplines preferred with 8+ years total combined experience or Masters with 5+ years
- 3+ years of experience in project management
- Demonstrated success leading cross-functional global teams in the medical industry (pharma or biotech)
- Experience across the full project lifecycle (discovery, requirements definition, development, launch and sustaining)
- Knowledge of regulatory pathways for drugs, biologics or combination devices
- Strong business acumen
- Effective communication and presentation skills
- Demonstrated self-starter who can quickly and efficiently manage continuous change; willing to challenge the norm when needed and drive to decisions
- Understanding and experience in good manufacturing procedures, good laboratory and product development process requirements
- Ability to work within a global team to understand project requests and translate requirements to the final project deliverables.
- Experience in creating and maintaining project deliverables (such as project timelines, meeting minutes, status reports)
- Knowledge of device and drug regulatory requirements
- PMP certification or equivalent
- Experience leading global R&D teams
- Master’s degree