Job Information
J&J Family of Companies Associate Director, Temperature Strategy & Execution in Titusville, New Jersey
Associate Director, Temperature Strategy & Execution - 2406177829W
Description
Johnson & Johnson Innovative Medicine Research & Development (JJIM R&D), part of the Johnson & Johnson Family of Companies, is recruiting for an Associate Director, Temperature Strategy & Execution within Clinical Supply Chain (CSC). The position can be located in Horsham, PA, Titusville, NJ, or Beerse, BE.
Within JJIM R&D, CSC holds the global responsibility for delivering all clinical supplies (Devices, API, Drug Product, Finished Kits) in the R&D portfolio. Our activities include all in-house and outsourced manufacturing, demand forecasting, supply planning, and global distribution of supplies to more than 145,000 patients in over 85 countries in more than 400 clinical trials every year.
As the Associate Director, Temperature Strategy & Execution, you will be responsible for leading a team, setting the strategic direction and the operational management of temperature-related matters for the worldwide distribution activities of clinical supplies for synthetics, biologics, vaccines and advanced therapies during all phases of clinical trials, consistent with GxP guidelines. You will develop and implement new solutions and make improvements to existing solutions and processes.
Key Responsibilities:
Lead the Temperature Strategy & Execution (TS&E) team, modelling conscious inclusion and J&J Leadership Characteristics.
Develop and recruit diverse talents.
Accountable for TS&E processes, including Audits & Inspections, Temperature Excursion Assessment, and Temperature related base business escalations.
Oversee TS&E governance within Clinical Supply Chain (CSC) and within partner organizations (i.e. Quality, Drug Product Development, Analytical Development, Global Clinical Operations).
Ensure TS&E activities are consistent with all Standard Operating Procedures (SOP) and GxP, Quality, and Regulatory guidelines, contributing to successful subject dosing within Pharma R&D
Develop and lead future-state strategy for TS&E focused on enhanced processes, governance, and technology, in alignment with cross-functional stakeholders.
Own requirements on how Clinical Supplies should be monitored and controlled during transit to and storage at Investigational Sites and Depots
Accountable for passive shipper and temperature monitoring device strategy in CSC, including requirements, performance standards, evolution, and day to day oversight.
Conduct TS&E as a center of excellence, addressing temperature management requirements for storage and transit of study drug.
Develop strong internal collaboration with and influence functional and cross-functional stakeholders (including CSC, Commercial Quality, Deliver, Global Development, Drug Product Development, Analytical Development, Compliance, CSC QA) to ensure base business execution and anticipate upcoming needs and drive synergies when developing new capabilities.
Support changes to the portfolio including new trials, strategies, modalities, licensing & acquisitions, and business integrations.
Proactively apply data and metrics to drive continuous improvement and sponsor continuous improvement initiatives across the end-to-end logistics’ team.
Qualifications
Qualifications
Education:
A minimum of a Bachelor’s degree is required with a focus in engineering, business, supply chain or technical sciences.
A Master's degree as well as other certifications including APICS, Project Management (PMP, FPX), Six Sigma or Lean are preferred
Required:
A minimum of 8 years of relevant professional experience in pharma/life sciences.
Experience with minimum one the following functions: clinical operations, logistics, distribution, operations, temperature management, temperature monitoring devices, quality assurance, supply chain planning, and/or analytical development.
Demonstrated people leadership and talent development experience.
Experience in defining a vision, strategy and driving its execution
Demonstrated ability to improve processes end-to-end
Ability to work in a fast-paced global environment both independently and collaboratively at various levels across the organization and with external service providers
Strong interpersonal skills and demonstrated ability for strong collaboration
Ability to work in a highly regulated environment.
Preferred:
Knowledge of Clinical Supply Distribution, Clinical Study Execution, and GxP principles.
Solid understanding of ambient, cold, frozen and/or deep frozen (cryo) distribution requirements
Experience with clinical supply management tools preferred
Experience with quality system tools preferred
Intermediate to advanced software skills preferred (e.g., Microsoft Excel, PowerPoint)
The anticipated compensation for this role is $135,000-$232,300.
The compensation information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be
eligible for compensation and benefits in accordance with their local market.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability
Primary Location NA-US-Pennsylvania-Horsham
Other Locations Europe/Middle East/Africa-Belgium-Antwerp-Beerse, NA-US-New Jersey-Titusville
Organization Janssen Research & Development, LLC (6084)
Job Function Clinical Supply Operations
Req ID: 2406177829W