Jobs · Pennsylvania

Senior Scientist, Biotherapeutics R&D

Johnson & Johnson Innovative Medicine · Malvern, PA · 4 days ago
HybridFull-time

About the role

This position is a hybrid role and will be located in Malvern, PA. The Senior Scientist, Biotherapeutics R&D will manage, negotiate, and execute license and business continuity agreements for cell lines and critical reagents.

Responsibilities

  • Independently hypothesize, design and execute projects or analysis with hands-on involvement.
  • Ensure the availability of cell lines and critical reagents governed by contract.
  • Guide the examination of standard procedures and improve current approaches.
  • Engage with Legal to confirm Freedom to Operate and status of Intellectual Property.
  • Manage historical contract knowledge and optimize contract tracking and payment.
  • Communicate regularly with business functions responsible for contract generation and maintenance including Procurement, Contracting, Totality and others.
  • Collaborate across research groups to share results.
  • Leverage the work of project members to meet project checkpoints and accomplish team objectives on time and within budget.

Qualifications

  • A minimum of a Bachelor's degree in Biology, Pharmacology, Immunology, Biochemistry, or other relevant scientific discipline is required.
  • An advanced degree (Master’s, Ph.D.) in Biology, Pharmacology, Immunology, Biochemistry, or other relevant scientific discipline is preferred.
  • A minimum of 5 years of relevant industry experience with a Bachelor’s degree; a minimum of 3 years of relevant industry experience with a Master's degree; or a minimum of 1 year of relevant industry experience with a Ph.D. is required.
  • Experience with method development is required.
  • Understanding of the critical components for method development is required.
  • Understanding of cell lines and critical reagent methods is preferred.
  • Knowledge of the requirements and obligations for analytical method components for use in the release of clinical and commercial products is preferred.
  • Knowledge of execution of scientific contracts and licenses is preferred.
  • Demonstrated ability to collaborate with internal and external stakeholders is required.
  • Excellent verbal and written communication skills are necessary.
  • A strong attention to detail and organizational skills are essential.
  • Strong problem-solving skills are required.
  • The ability to work independently with minimal supervision to meet tight deadlines is required.
  • The ability to engage with cross-functional teams and Business and Quality groups to drive the execution of agreements is required.

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