Johnson & Johnson Innovative Medicine
Global Head, Life Cycle Management ATSC MSAT
Johnson & Johnson Innovative Medicine, Raritan, New Jersey, us, 08869
Global Head, Life Cycle Management ATSC MSAT
Johnson & Johnson Innovative Medicines is recruiting for the Advanced Therapies Manufacturing Science and Technology (MSAT) organization. This role is part of the Global Head, Life Cycle Management for ATSC MSAT, where you will work to scale high‑quality cell and gene therapy products worldwide.
Job Function:
Supply Chain Engineering Job Sub Function:
Manufacturing Engineering Job Category:
People Leader
Locations:
Raritan, New Jersey; Spring House, Pennsylvania
Requisition Numbers:
United States – R-031792; Belgium – R-032748
Apply today for this exciting opportunity to be part of the team! The role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. We invite candidates from any location to apply.
Responsibilities
Own the advanced therapies product technology roadmaps; lead cross‑functional and cross‑sector teams in the strategic development of high‑value solutions required to achieve goals in technology, science, facilities, processes and products.
Lead product roadmap business planning strategies in partnership with value chain and manufacturing platforms across a matrix of functions to define and advance business process models, leading change with positive energy.
Lead a team of technical product owners to ensure deep product and process understanding is scaled across advanced therapies platform and that robust and reliable manufacturing processes are in place across the advanced therapies manufacturing network.
Translate strategic product roadmaps to detailed execution plans for programs in order to deliver on target outcomes and enhance the lifecycle of the product.
Oversee implementation in partnership with DPDS of life cycle management, new technology and automation projects across manufacturing sites to improve robustness, scalability and cost of goods/cycle time/right‑first‑time for products, delivering measurable impact.
Ensure technical and manufacturing requirements are addressed throughout the lifecycle of new solutions.
Drive continuous improvement and foster an operational excellence culture to enhance productivity and efficiency of operations.
Proactively align decision making with enterprise‑wide strategy, evaluating short‑and long‑term goals against potential consequences.
Champion data solutions throughout the organization to ensure robust products and processes throughout the lifecycle of the products.
Devise strategies and solutions to deliver on rapid growth ambitions, including enhancing reliability, compliance, and efficiency of product value chains end‑to‑end.
Establish organizational capability build roadmap – defining current state to ideal state process, systems, data, and performance measures and ensure execution of fit‑for‑purpose training and learning across the advanced therapies platform.
Maintain a robust technical support network related to lifecycle management, new technologies, automation, comparability, change management, and tech transfers for products, including material science assessments, sourcing strategies, and critical to quality processes.
Qualifications
University/Bachelor’s Degree in Science/Engineering or Equivalent with 12–14 years Biotech/Pharmaceutical experience or Masters/PhD degree in Engineering, with 10+ years Biotech/Pharmaceutical experience or equivalent industry experience.
Hands‑on experience in Manufacturing Operations and/or R&D in a biopharmaceutical manufacturing setting (e.g., cell/gene therapy products, vaccines, or any other advanced therapy products).
Experience leading technology transfer activities and technical services for cell/gene therapies.
Excellent technical skills and problem‑solving skills.
Knowledgeable in manufacturing sciences, cGMP compliance, change management methodology, and advanced therapies product regulatory and validation requirements.
Knowledge of data analytics/statistics and process automation.
Ability to lead and influence multidisciplinary, cross‑functional teams in an international environment.
Project‑dependent travel.
Compensation expectations for this role: $173,000 – $299,000.
Johnson & Johnson is an 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, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.
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Job Function:
Supply Chain Engineering Job Sub Function:
Manufacturing Engineering Job Category:
People Leader
Locations:
Raritan, New Jersey; Spring House, Pennsylvania
Requisition Numbers:
United States – R-031792; Belgium – R-032748
Apply today for this exciting opportunity to be part of the team! The role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. We invite candidates from any location to apply.
Responsibilities
Own the advanced therapies product technology roadmaps; lead cross‑functional and cross‑sector teams in the strategic development of high‑value solutions required to achieve goals in technology, science, facilities, processes and products.
Lead product roadmap business planning strategies in partnership with value chain and manufacturing platforms across a matrix of functions to define and advance business process models, leading change with positive energy.
Lead a team of technical product owners to ensure deep product and process understanding is scaled across advanced therapies platform and that robust and reliable manufacturing processes are in place across the advanced therapies manufacturing network.
Translate strategic product roadmaps to detailed execution plans for programs in order to deliver on target outcomes and enhance the lifecycle of the product.
Oversee implementation in partnership with DPDS of life cycle management, new technology and automation projects across manufacturing sites to improve robustness, scalability and cost of goods/cycle time/right‑first‑time for products, delivering measurable impact.
Ensure technical and manufacturing requirements are addressed throughout the lifecycle of new solutions.
Drive continuous improvement and foster an operational excellence culture to enhance productivity and efficiency of operations.
Proactively align decision making with enterprise‑wide strategy, evaluating short‑and long‑term goals against potential consequences.
Champion data solutions throughout the organization to ensure robust products and processes throughout the lifecycle of the products.
Devise strategies and solutions to deliver on rapid growth ambitions, including enhancing reliability, compliance, and efficiency of product value chains end‑to‑end.
Establish organizational capability build roadmap – defining current state to ideal state process, systems, data, and performance measures and ensure execution of fit‑for‑purpose training and learning across the advanced therapies platform.
Maintain a robust technical support network related to lifecycle management, new technologies, automation, comparability, change management, and tech transfers for products, including material science assessments, sourcing strategies, and critical to quality processes.
Qualifications
University/Bachelor’s Degree in Science/Engineering or Equivalent with 12–14 years Biotech/Pharmaceutical experience or Masters/PhD degree in Engineering, with 10+ years Biotech/Pharmaceutical experience or equivalent industry experience.
Hands‑on experience in Manufacturing Operations and/or R&D in a biopharmaceutical manufacturing setting (e.g., cell/gene therapy products, vaccines, or any other advanced therapy products).
Experience leading technology transfer activities and technical services for cell/gene therapies.
Excellent technical skills and problem‑solving skills.
Knowledgeable in manufacturing sciences, cGMP compliance, change management methodology, and advanced therapies product regulatory and validation requirements.
Knowledge of data analytics/statistics and process automation.
Ability to lead and influence multidisciplinary, cross‑functional teams in an international environment.
Project‑dependent travel.
Compensation expectations for this role: $173,000 – $299,000.
Johnson & Johnson is an 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, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.
#J-18808-Ljbffr