**Role**:
- Manage a team of Project Managers supporting all client projects in the facility, overseeing project activities from kick-off to project closure; Drive the implementation of new projects into the operations via a collaborative oversight of the cross-functional project management efforts;
- Develop a baseline project implementation/execution strategy as part of initial qualification process for new business; Support the business development activities of evaluating and assessing strategic fit for new projects into the facility, via business analysis, resources analysis, and capability fit;
- Ensure project deliverables are client focused, results oriented, performance driven, and in compliance with all applicable internal and external requirements;
- Effectively work with management to ensure on time delivery of all client projects in the facility and identify risk mitigation plans, when applicable;
- Project Management Team and Leadership Development
- NPIx Gate Review Management
- NPI Ship Date and Revenue Forecasting
- QuickBase Management
- Customer Temperature Management
- On Time Product Development Deliverables (pre-clinical, clinical, process validation)
- Project Planning Aptitude
- Timeline Management
- Project Risk Management
- Escalation Communication Management
- Project Governance and Communication Templates
- Development Revenue Forecasting Accuracy
- Stakeholder & Communication Management Support aligned, metrics-based reporting of site product development performance at business unit-level and company-level report outs.
**Education**:
- Master's Degree/Ph.D.
in a scientific discipline, Management, or related field
- M.B.A. (nice to have)
- PMP (nice to have)
**Experience**:
- 10+ years of in Management positions and or Project Management leadership experience in a biotechnology or related field
- Demonstrated, proficient customer experience/customer service management
- Experience working in contract development and manufacturing space, beneficial
- Demonstrated mastery of Project Management theories and principles
- Project development
- Project execution
- Project monitoring & controlling
- Project close out
- Working knowledge in the use of a wide variety of equipment and data systems in support of development tech transfer and validation strategies.
- Working knowledge and hands-on experience with biological manufacturing and validation concepts and procedures in a GMP environment.
- Previous experience in performance management, developing staffing plans, and mentoring team members.
**Location**: Anagni
**Catalent offers rewarding opportunities to further your career!
** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.
Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us.
Join us in making a difference.
Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.
As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone's safety.
The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.
personal initiative.
dynamic pace.
meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
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