Johnson & Johnson Innovative Medicine
Project Manager, Site Material Logistics, CAR-T
Johnson & Johnson Innovative Medicine, Raritan, New Jersey, us, 08869
Overview
Project Manager, Site Material Logistics, CAR-T – onsite position located in Raritan, NJ. Johnson & Johnson Innovative Medicines and Legend Biotech have a global collaboration to develop, manufacture, and commercialize CAR-T therapies. This role leads cross-functional CAR-T initiatives within the Advanced Therapies division, with strong program governance, end-to-end planning, and the ability to translate complex manufacturing needs into actionable projects across functions.
Responsibilities
Lead cross-functional project teams in a matrix environment to plan, execute, and deliver CAR-T initiatives including manufacturing, tech transfers, warehousing and logistics, cryopreservation, and related programs.
Own project charters, governance structures, milestones, budgets, resource plans, and risk management; ensure on-time, within-scope, and within-budget delivery aligned with site and enterprise objectives.
Develop and maintain up-to-date project timelines with critical milestones, interdependencies, financial commitments, and resource constraints using appropriate scheduling techniques.
Monitor project status and execution; report updates via project templates and dashboards; prepare agendas, minutes, and metrics for teams.
Provide transparent verbal and written communication to teams, stakeholders, and appropriate levels of the organization.
Lead After Action Reviews, share lessons learned, and integrate improvements into processes, tools, and templates.
Assist in regulatory inspections, safety and quality audits; follow GMP and safety guidelines and regulations.
Qualifications Education:
Bachelor’s degree required; MBA, MS, or related field preferred.
Experience and Skills
Required:
Minimum 8 years of experience in supply chain, logistics, or manufacturing operations.
Proven record of project management leading multi-functional and cross-functional teams.
Excellent verbal and written communication and presentation skills.
Strong project management, strategic thinking, financial acumen, and problem-solving capabilities.
Solid understanding of GMP/regulatory requirements and site quality systems; exposure to audit processes is a plus.
Preferred:
Minimum 3 years in roles supporting regulated GMP and/or cell/gene therapy environments.
PMP, FPX, Lean Six Sigma, or other PM certifications; supply chain/operations certifications (e.g., APICS CPIM/CSCP) are a plus.
Travel up to 10% domestically and/or internationally may be required.
Other
Location: Raritan, New Jersey. This position may require travel.
Equal Opportunity Employer. All qualified applicants will receive consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by law. See company accessibility resources and benefits for details.
Note: This description retains the core job information and expectations from the original posting while removing extraneous site-navigation elements and repetitive UI prompts.
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Responsibilities
Lead cross-functional project teams in a matrix environment to plan, execute, and deliver CAR-T initiatives including manufacturing, tech transfers, warehousing and logistics, cryopreservation, and related programs.
Own project charters, governance structures, milestones, budgets, resource plans, and risk management; ensure on-time, within-scope, and within-budget delivery aligned with site and enterprise objectives.
Develop and maintain up-to-date project timelines with critical milestones, interdependencies, financial commitments, and resource constraints using appropriate scheduling techniques.
Monitor project status and execution; report updates via project templates and dashboards; prepare agendas, minutes, and metrics for teams.
Provide transparent verbal and written communication to teams, stakeholders, and appropriate levels of the organization.
Lead After Action Reviews, share lessons learned, and integrate improvements into processes, tools, and templates.
Assist in regulatory inspections, safety and quality audits; follow GMP and safety guidelines and regulations.
Qualifications Education:
Bachelor’s degree required; MBA, MS, or related field preferred.
Experience and Skills
Required:
Minimum 8 years of experience in supply chain, logistics, or manufacturing operations.
Proven record of project management leading multi-functional and cross-functional teams.
Excellent verbal and written communication and presentation skills.
Strong project management, strategic thinking, financial acumen, and problem-solving capabilities.
Solid understanding of GMP/regulatory requirements and site quality systems; exposure to audit processes is a plus.
Preferred:
Minimum 3 years in roles supporting regulated GMP and/or cell/gene therapy environments.
PMP, FPX, Lean Six Sigma, or other PM certifications; supply chain/operations certifications (e.g., APICS CPIM/CSCP) are a plus.
Travel up to 10% domestically and/or internationally may be required.
Other
Location: Raritan, New Jersey. This position may require travel.
Equal Opportunity Employer. All qualified applicants will receive consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by law. See company accessibility resources and benefits for details.
Note: This description retains the core job information and expectations from the original posting while removing extraneous site-navigation elements and repetitive UI prompts.
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