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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.

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We are searching for the best talent for a Scientific Director Discovery Pharmaceutics to be located in Spring House PA.

Purpose: Global Discovery Pharmaceutics is part of the Pharmaceutical Development & Supply (PPDS) organization within the Discovery Product Development and Supply (DPDS) division of Johnson & Johnson Innovative Medicine (JJIM). The group supports drug discovery programs from hit-to-lead through candidate selection with a focus on the Synthetics Modalities portfolio including small molecules degraders peptides oligonucleotides and conjugates.

As the Scientific Director you and your team will provide expert scientific leadership to enable informed molecule design and developability decisions. You will collaborate in close partnership with chemistry biology pharmacokinetics and pre-clinical safety.

As head of the team you will provide scientific strategic and people leadership while driving the CMC deliverables for discovery programs. Your responsibilities include physical characterization biopharmaceutical evaluation and preclinical formulation support across diverse routes of administration - including oral parenteral and intra-organ - and may include other advanced drug delivery strategies as required.

You will be responsible for:

• Leading and developing a multidisciplinary scientific team building technical depth mentoring talent fostering a culture of collaboration innovation and continuous improvement.
  
• Developing innovative screening tools and formulation approaches with the capability of meeting rapid cycle times and miniaturization to influence and enable early discovery. Collaborating with academia and industry experts.
  
• Enhancing digital tools data analytics and computational approaches to support developability assessments and improve the quality and speed of decision making in discovery programs.
  
• Enabling and overcoming exposure challenges for critical tool compounds or non-optimized leads with enabling formulations in support of PK PK/PD translational pharmacology and tolerability studies.
  
• Influencing compound design early to ensure lead candidates have the desired properties for specific drug delivery platforms and technologies to ensure patient convenience and compliance.
  
• Portfolio delivery and accelerating the transition from discovery to development through collaboration with key development functions to support the GLP toxicology studies formulation strategy and dosage form design for clinical studies.
  
• Influencing risk management and mitigation.

Qualifications / Requirements

Education:

• A PhD in Pharmaceutical Sciences Chemistry Chemical Engineering or a related field with 12 years of relevant experience OR a Masters degree with 18 years of relevant experience is required.
  

Experience and Skills:

• Demonstrated people leadership and talent development including technical and non-technical coaching and mentoring is required.
  
• Ability to drive and get results through leading others is required.
  
• Strong understanding of Discovery and Pharmaceutical Development including ADME Preclinical Safety evaluation and Drug Development is required.
  
• Proven experience in developability assessments for synthetic modalities in the area of molecular design interpretation of pharmaceutical properties in relation to exposure and toxicology data setting formulation strategies is required.
  
• Track record of scientific contributions is required.
  
• Excellent communication critical thinking and problem solving skills are required.
  
• Strong collaboration and networking capabilities are required.
  
• Willingness to take informed risks or leave appropriate knowledge gaps as needed to maintain speed and program progression.
  

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 & 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 external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource.

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