• Distinguished Scientist, Protein Conjugates

    J&J Family of Companies (Malvern, PA)


    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:

    Discovery & Pre-Clinical/Clinical Development

    Job Sub** **Function:

    Biotherapeutics R&D

    Job Category:

    Scientific/Technology

    All Job Posting Locations:

    Malvern, Pennsylvania, United States of America, Spring House, Pennsylvania, 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 a Distinguished Scientist, Protein Conjugates to be located in** **Malvern, PA or Spring House, PA,

    Purpose:

    Within the CMC group, you will lead multiple CMC Teams spanning from pre-NME through post-Approval, including Life Cycle Management (LCM). You will be the CMC point of contact with the Compound Development Team(s) (CDT) and Value Stream Teams (VST).

    You will be responsible for:

    + the creation and implementation of the development strategy, the adherence to the CMC 12 Stage process, approval by governance bodies, the identification and mitigation of CMC risks, the completion of required CMC regulatory documents and responses, creation and adherence to budget and timelines, and the delivery of clinical and launch drug supplies in accordance with development plans.

    + seeing opportunities for team or product development improvements across the TDS organization. They may also support or lead teams in implementing initiatives to deliver organizational or process improvements.

    + demonstrating behaviors consistent with the current Leadership Imperatives and will be mentoring and coaching CMC Team Members to improve their skills and contributions to the organization in collaboration with line management.

    + focusing on development projects which may span multiple Therapeutic Areas (TAs) and/or Innovative Medicine Supply Chain (IMSC) and stages of development.

    + working in a multi-disciplinary, complex and innovative environment, with evidence of delivering results in this setting, including in-depth experience and technical knowledge of the Large Molecule CMC protein and Bioconjugates (include Antibody Drug Conjugates and radio-ligand therapy) development process, preferably including an understanding of early, late and LCM development.

    Qualifications / Requirements:

    Education:

    + a minimum of a Bachelor’s degree in life science or related field is required

    + a Master's degree or Ph.D in life science or related field is highly preferred

    Required:

    + a minimum of 10 years relevant experience is required. A combination of industry & post doc experience is acceptable

    + Large Molecule CMC experience is required.

    + Excellent communication skills, both oral and written, as well as proven conflict management and negotiation skills are required

    + Excellent interpersonal skills with the ability to adapt effectively to a constantly evolving organization issues, structures and dynamics is required

    + Experience in setting development and regulatory strategies for products in development is required

    + Demonstrated capability to manage multiple projects is required.

    + Ability to make difficult decisions in a timely fashion along with excellent follow through and organizational skills to assure team and organizational alignment to these decisions is required

    Preferred:

    + Experience in developing antibody drug conjugates or radio-ligand therapy is highly preferred

    + Influencing ability without line authority is preferred

     

    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 ( [email protected] ) or contact AskGS to be directed to your accommodation resource.