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Senior Medical Science Liaison-Autoantibody
Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
People Leader
All Job Posting Locations:
Boston, Massachusetts, United States of America, White Plains, New York, United States
Job Description:
Johnson & Johnson Innovative Medicine is searching for the best talent for a Senior Medical Science Liaison- Autoantibody Pipeline for the Northeast region. This is a field-based position located in the Northeast region, the ideal location is the New York or Boston area. The territory covers Massachusetts, Connecticut, Rhode Island, Maine, New Hampshire, Vermont, and New York City.
About Immunology
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses. You can influence where medicine is going by restoring health to millions of people living with immune diseases. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine
The Senior Medical Science Liaison (Sr. MSL) is responsible for providing fair balanced, objective, scientific information and education to opinion leaders (OLs), health care professionals, and to internal partners as required by scientific and business needs.The Sr. MSL is considered an established scientific and clinical knowledge lead on current and future J&J Innovative Medicine products per Therapeutic Area (TA) alignment.The Sr. MSL is responsible for staying abreast of current scientific and treatment landscape trends in their therapeutic areas of interest.The Sr. MSL provides research support for company and investigator-initiated research.The Sr MSL will function with high integrity and follow credo values.
The Sr. MSL is responsible for building external relationships with identified OLs and health care providers (MD, DO, PhD, PA, NP, RN, Pharm.D., bio coordinators) and developing and managing a geographical territory. These relationships and engagements can include both virtual & in-person, with a prioritization of in-person engagements when appropriate.
Johnson & Johnson Military – SkillBridge Internship (Future Opportunity)
Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
SkillBridge
Job Category:
Career Program
All Job Posting Locations:
Cincinnati, Ohio, United States of America, Danvers, Massachusetts, United States of America, El Paso, Texas, United States of America, Horsham, Pennsylvania, United States of America, Irvine, California, United States of America, Jacksonville, Florida, United States of America, Malvern, Pennsylvania, United States of America, New Brunswick, New Jersey, United States of America, Palm Beach Gardens, Florida, United States of America, Raritan, New Jersey, United States of America, Raynham, Massachusetts, United States of America, San Angelo, Texas, United States of America, Santa Clara, California, United States of America, Spring House, Pennsylvania, United States of America, Tampa, Florida, United States of America, Titusville, New Jersey, United States of America
Job Description:
Ready to Continue Your Leadership Journey? We believe people with military experience already possess many of the qualities that make for success in business settings. You know how to build consensus. You’ve demonstrated adaptiveness and agility in challenging environments. And you’ve put your skills and experience to the test in a variety of situations. With the power of the world’s largest and most broadly based healthcare company behind you, you can continue your leadership journey—and make an impact that touches the lives of people everywhere.
Launched in 2021, the Johnson & Johnson SkillBridge Program is our latest military-connected talent pipeline program. As an approved provider with the U.S. Department of Defense, we’re offering a best-in-class internship-to-hire pathway specifically designed to support career transitions for separating military service members. You’ll learn firsthand how teams at Johnson & Johnson are rising to the occasion, innovating and delivering global healthcare solutions in response to the most complex and urgent challenges of our time. In the course of the immersive program, you’ll continue your leadership journey while building highly in-demand skills to help support your successful transition to a civilian career.
Principal Data Scientist
Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science
Job Category:
Scientific/Technology
All Job Posting Locations:
Titusville, New Jersey, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Principal Data Scientist to be located in Titusville, NJ.
Purpose:
The Commercial Data Sciences & Data Insights team within Johnson & Johnson Innovative Medicine Business Technology organization is looking for an extraordinary Data Scientist who is passionate about crafting, developing, and fielding data science solutions that drive impact for patients and for Johnson & Johnson. There are many ways to explore and analyze data, and this powers the excitement and passion of data scientists at Janssen as many business units are eager to use the data to build business value.
You will be responsible for:
In this role you will be someone who stays on the cutting edge of artificial intelligence, data science and advanced analytics research through novel project execution and development of algorithms that influence decisions at various levels in the organization, including but not limited to sales and marketing optimization, patient/payer analytics, commercial strategy, and relate commercially-focused model development. The role requires both a broad knowledge of existing AI-type algorithms and the creativity to invent and customize when necessary. You will lead and deliver projects and develop solutions that in turn deliver insights. You will lead and work with matrixed teams across business and technology, and be part of a dynamic, accomplished organization that will support multiple therapeutic areas and commercial functions.
Qualifications / Requirements:
- Ph.D. with 3 years of experience, or M.S. with 5+ years of relevant pharma sales & marketing experience, in Computer Sciences, Statistics, Machine Learning & Artificial Intelligence, Physics, Molecular Biology, Bioinformatics, Computational Informatics, Medical Informatics, Computational Biology or a related discipline.
- Strong working knowledge of machine learning platforms/environments.
- Strong working knowledge of AI-type algorithms, including machine learning techniques such as regression, decision trees, probability networks, association rules, clustering, neural networks, and/or Bayesian models.
- Familiarity with large datasets, handling of healthcare relevant datasets and understanding of data analysis workflows.
- Proficiency with one or more programming language such as Python, R, SAS or Java.
- Proficiency with SQL.
- Experience with Pyspark.
- Experience delivering on data science projects using predictive technologies, data mining and/or text mining.
- Familiarity with working in a cloud-based technology stack.
- Familiarity with usage of Generative and Agentic AI for productivity improvement.
- Strong communication skills and ability to communicate complex methods and results to diverse audiences.
Preferred Qualifications:
- Experience in the commercial pharmaceuticals business.
- Experience with sales and marketing best practices, processes, and related technology.
- Working knowledge of commercially available healthcare data sets.
- Working knowledge of machine learning platforms/environments and experience implementing AI driven solutions (nice to have)
- Building end-to-end LLM powered solutions that drive business value
- Evaluation, validation, and refinement of LLM frameworks and generative AI applications
- Continual learning, prompting, and LLM fine tuning/PEFT
- Familiarity with open-source and gated/paid model landscape
Associate Medical Director US Medical Affairs -Gastroenterology
Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Affairs – MD
Job Category:
Scientific/Technology
All Job Posting Locations:
Horsham, Pennsylvania, United States of America
Job Description:
We are searching for the best talent for Associate Medical Director, US Medical Affairs -Gastroenterology based in Horsham, PA.
About Immunology
Our expertise in Innovative Medicine is informed and inspired by patients and healthcare professionals, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses. You can influence where medicine is going by restoring health to millions of people living with immune diseases.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Purpose:
J&J Innovative Medicine is seeking an Associate Medical Director, US Medical Affairs -Gastroenterology to be a key member of the US Medical Affairs Immunology team, where you will influence product development, scientific communication, and evidence generation efforts, ensuring alignment with business objectives and regulatory standards.
This position resides in the Medical Affairs Gastroenterology Therapeutic Area (TA) Team which is responsible for developing, coordinating and executing the Therapeutic Area strategic plan for Medical Affairs. This therapeutic area strategic plan seeks to identify and address key stakeholders’ knowledge gaps through data dissemination, data generation and education. The Medical Affairs Therapeutic Area (TA) teams are also responsible for designing and executing registries, Phase IIIb/IV trials and any post-marketing requirements within the areas of J&J Innovative Medicine Immunology’s current or emerging gastroenterology assets in both adult and pediatric US indications. The Therapeutic Area (TA) team includes Medical Affairs Physicians, Research Scientists, Integrated Evidence Team (IET) Leaders, and Medical Affairs Operations members.
The Associate Medical Director US Medical Affairs -Gastroenterology will report to the Head, Gastroenterology US Medical Affairs- Immunology, and be an important part of the Gastroenterology TA team, working closely with the other Gastroenterology Medical Directors (and Associate Directors) as well as partners in Global Medical Affairs, Real World Value and Evidence (RWV&E), Population Health, Epidemiology, R&D, Biostatistics, and US and Global Commercial Team members supporting Immunology and Gastroenterology within the Johnson & Johnson organization. The Associate Medical Director, Gastroenterology will be responsible for leading the development and execution of Medical Affairs sponsored and supported clinical programs for company products in the Gastroenterology Therapeutic Area and will partner with other GI team members and cross-functional partners to formulate and execute scientific strategy on marketed products as well as address other medical questions and issues that arise from the field and experts in inflammatory bowel disease. The Associate Medical Director, Gastroenterology will also lead or contribute to development of related abstracts and manuscripts as either an author or reviewer.
You will be responsible for:
- Serve as the Study Responsible Physician (SRP) for one or more studies, responsible for the development and execution of these Medical Affairs sponsored and supported clinical programs for company products in the Gastroenterology TA, with mentorship and supervision. This will include study design, protocol development, regulatory communications, academic and community-based IBD HCP and investigator interactions, support of execution, and supervision of clinical studies of all types, including: Phase IIIb/IV, registries, real world evidence, and investigator-initiated studies and collaborations supported by US Medical Affairs within the TA.
- Contributes to US GI Medical Affairs strategy, working cross-functionally with partners within the GI Integrated evidence team (IET), including RWV&E, IET Leads, SCG, Marketing brand teams, as well as potentially IBD Disease Area Stronghold (DAS), R&D, Global Medical Affairs, Medical Science Liaison (MSL) and Global Commercial partners to promote and execute the GI TA Strategy for establishing access as well as evidence generation and dissemination.
- Contributes to the preparation of regulatory submissions and interactions with Health Authorities (and particularly the US FDA) and helps to ensure regulatory post-marketing commitments are efficiently satisfied with cost-effective, efficient, and scientifically rigorous methods.
- Contributes as a subject matter expert on previous and new data in support of US Immunology approved (or planned) GI drugs and indications, partnering particularly with respective marketing brand teams (as well as other commercial and IET partners, including RWVE, SCG, V&E Field and Med Info and other CAC partners)
- Actively partners with individuals in Gastroenterology TA and other groups inside and outside Medical Affairs (e.g. Biostats, GCO, Regulatory Affairs, QA and QC) to create Analysis Plans, safety data review for database locks and ensure compliance with study monitoring and other SOP/GCP requirements (and support audits, as needed).
- Contributes to or leads the development of abstracts and manuscripts related to J&J supported and sponsored studies, with a focus on IBD-related efficacy, outcomes, and safety/adverse event analyses.
- Builds and manages effective relationships with key opinion leaders and investigators related to Medical Affairs studies and strategic initiatives.
Qualifications /Requirements
- MD/DO degree (or international equivalent) is required. Current or prior Board Certification or Eligibility in Gastroenterology or Immunology is preferred
- Pharmaceutical industry interaction and/or experience and/or post-graduate clinical medical practice with experience in clinical immunology/gastroenterology and/or experience with clinical studies, registries, epidemiology or health outcomes required
- Experience in gastroenterology, particularly in inflammatory bowel disease highly preferred
- Experience with the planning and execution/writing of regulatory submissions, protocols, and/or scientific manuscripts preferred
- Experience with data analysis and review, and/or clinical study execution as either an investigator or a medical monitor or clinical scientist preferred
- Experience with the clinical use or clinical study of immunologic biologics and small molecules preferred
- Strong organizational, written, and verbal communication skills, including proficiency in effective and impactful oral presentations required
- Strong time management skills with the ability to be accountable for deliverables and timelines required
- The ability to work in a matrix environment, collaborating effectively with many cross functional partners and succeed in participating in and leading cross functional teams required
- Energy and enthusiasm, leadership skills and potential, and the ability and desire to embrace building new expertise are essential
- Approximately 10% to 20% annual travel is generally required (primarily domestic, occasionally international).
- This position is located in Horsham, PA and follows a hybrid schedule of three days in the office and two days remotely per week
Sterilmed E2E Supply Chain Leader
Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Manufacturing
Job Sub Function:
Multi-Family Supply Chain Manufacturing
Job Category:
People Leader
All Job Posting Locations:
Plymouth, Minnesota, United States of America
Job Description:
Johnson & Johnson is currently recruiting for a Sterilmed E2E Supply Chain Leader to be based in Plymouth, MN.
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
Job Summary
- Accountable for the E2E Supply Chain performance of the Sterilmed platform and the development and execution of the overall Supply Chain strategy and framework, in alignment with Commercial and CSS Supply Chain strategies.
- Reports to the CSS Supply Chain Vice President and is part of the Sterilmed Leadership team.
- Direct reports to this position are the following Sterilmed functions: Research and Development, E2E Product Management, E2E Planning, External Manufacturing, and E2E Technical Life Cycle Management.
Responsibilities:
- Drive strategic, tactical, and operational responses to commercial needs and interface with other global/regional CSS/HMD and JJSC functions as appropriate.
- Provide supply chain leadership and serve as a CSS Supply Chain voice in the Sterilmed platform leadership team with accountability for building an integrated Sterilmed Supply Chain strategy while having oversight over Research and Development and all supply chain functions including E2E Planning, E2E Product Management, External Manufacturing, and E2E Technical Life Cycle Management.
- Develop and implement an E2E supply chain model for the Sterilmed platform to support commercial requirements, providing leadership in translating commercial insights and strategy into Sterilmed SC strategy and deliverables.
- Deliver Sterilmed’s supply chain objectives and deliverables, including Sterilmed’s supply chain dashboard and KPI results.
- Drive flawless execution in new product launches, integration of new plants, and network optimization while contributing to the improvement of gross profit.
- Collaborate with Quality organizations to drive the implementation of quality and reliability improvement strategies and programs.
- Collaborate with the R&D teams of Operating Companies to ensure successful product launches while driving Design-to-Value programs that contribute to gross profit improvement,
- Anticipate risks and develop corresponding contingency plans to proactively manage product opportunities throughout the product lifecycle.
- Proactively manage the team to address product issues and improvement opportunities through the product lifecycle.
- Create an environment of calculated risk-taking, innovation, and creativity to continuously improve processes and increase efficiency.
- Secure the funds through the financial process for the launch of new products and support the life cycle of existing products.
- Work across organizational boundaries through influence, negotiation, and partnership with internal and external partners.
- Leverage MedTech and CSS processes, capabilities, and competencies to improve operational and business performance.
- Implement the necessary talent management strategy to build E2E supply chain capabilities.
- Create an engaging Credo-based culture.
- Communicate business-related issues or opportunities to next management level in a timely manner
Qualifications:
Experience and Education
- A minimum of a bachelor’s degree, preferably in Engineering. MBA or Master’s Degree in Engineering are preferred.
- A minimum of 10 years of supply chain experience is required, preferably in Medical Devices.
- Experience in supply chain positions that span across multiple disciplines (e.g. Manufacturing, Planning, Supply Chain Management, Technical Service Support, New Product Introduction) is preferred.
- A minimum of 10 years of people-manager experience is preferred.
- A proven track record of building high-performing organizations and people management skills in a global environment (coaching, people development, strategic workforce planning) is preferred.
Knowledge, Skills, & Abilities
- In-depth knowledge of product life cycle optimization, and a proven track record in launching new products in a complex global environment is preferred.
- A deep understanding of supply chain capabilities including cost of services is preferred.
- Deep expertise in Product & Process Development is preferred.
- Strong written and oral communication skills are required.
- Strong business acumen including financial processes, business case development, P&L calculation, and Cost-of-Goods-Sold (COGS) is preferred.
- Demonstrated global collaboration across global/regional teams is preferred.
- Flexible hours to accommodate US, EMEA and APAC work schedules as required.





