Johnson & Johnson Titusville , FL 32781
Posted 3 weeks ago
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At the Janssen Pharmaceutical Companies of Johnson & Johnson we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com and follow us @JanssenGlobal.
The ATSC New Site Project Leader is fully accountable from start to regulatory approval for leading the project team that will deliver a New Greenfield CART Manufacturing facility to be located in the USA (TBD). This plant will supply lifesaving medicines for patients for J&JIM.
The new site startup leader will be responsible for shaping the overall planning of the project, development of a new manufacturing site location including engineering, construction, equipment delivery, commissioning & qualification, hiring and training program for all new J&J employees, startup and FDA regulatory approval of the first product.
The plant will employ ~850 FTE when in full operation (80%/20% - JNJ vs Contractor) and will require approximately 1000 + engineers, equipment vendors and craftsman to design & build the facility. Overall schedule for new facility from CAR) to commercial FDA approval is 5 years.
Evaluate and recommend suitable sites for cell therapy facilities, considering factors such as location, infrastructure, regulatory compliance, and scalability.
Work closely with cross-functional teams, including scientists, regulatory affairs, and operations, to ensure alignment of engineering activities with business goals.
Collaborate with architects, contractors, vendors, and regulatory authorities to ensure compliance with relevant guidelines, codes, and regulations.
Develop project budgets and timelines, monitor progress, and manage resources to ensure timely and within-budget project completion.
Review engineering drawings, equipment specifications, and performance criteria to ensure the functional requirements of cell therapy manufacturing and research processes are met.
Coordinate with internal stakeholders and external consultants to optimize facility layout, infrastructure, utilities, HVAC systems, and cleanroom environments.
Collaborate with regulatory affairs and quality teams to manage inspections, audits, and any necessary corrective actions to maintain regulatory compliance.
Establish quality management systems and processes to support site build activities, ensuring documentation completeness and adherence to relevant regulations.
Foster a collaborative and inclusive work environment, promoting effective communication and teamwork.
Identify training and professional development opportunities for team members to enhance their skills and knowledge.
Additional Responsibilities:
Develop and align with the Sponsor on the Project Case and Final Project Objectives
Lead and facilitate Project / Site Leadership Alignment Meeting
Establish roles and responsibilities for all core team members.
Align and motivate core team members to feel fully accountable and engaged towards delivering their respective individual accountabilities.
Lead team to identify and manage risk throughout project.
Remove barriers to success and be available to support team.
Formally close project and recognize success including benchmarking.
Ensure required project financials and schedule controls. Cashflow management is essential.
Maintain budget, schedule, and ensure quality completion of deliverables.
Ensure occurrence of the Strategic Project Execution Planning session and confirm participation of the Sponsor and all Key Stakeholders
Manage communications with external regulatory authorities and the local community to ensure alignment with project objectives.
Manage relationship with J&J Corporate groups
The anticipated base range for this role is: $163,000-$282,900.
Johnson & Johnson