Johnson & Johnson

Principal Scientist, Biopharmaceutics

Johnson & Johnson$120K — $150K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. in Pharmaceutical Sciences, Chemical Engineering, or PharmD in Pharmacy required
  • Minimum of 3 years in biologics product development
  • Experience with PK and PBPK modeling preferred
  • Familiarity with IVIVC or similar approaches preferred
  • Understanding of biologics formulation principles preferred
  • Experience with drug-device integration preferred
  • Excellent verbal and written communication skills

Responsibilities

  • Design and execute studies on SC absorption and bioavailability
  • Develop IV-to-SC and SC-to-SC bridging strategies
  • Support biocomparability assessments for Drug Substance or Drug Product changes
  • Drive innovation in formulations and delivery devices
  • Collaborate with Drug Delivery Systems on combination product development
  • Develop in vitro and in silico tools for formulation selection
  • Represent Biopharmaceutics on product development teams

Benefits

  • Hybrid work model
  • Opportunity for mentorship and technical excellence promotion
  • Involvement in innovative biopharmaceutics projects
  • Access to professional development resources
  • Collaboration with cross-functional teams
Full Job Description
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 Job Description: Johnson & Johnson Innovative Medicine R&D is recruiting for a Principal Scientist, Biopharmaceutics.  This position is a hybrid role and will be located in Malvern, PA. We are seeking a highly motivated Principal Scientist to join the Biopharmaceutics team in the Drug Product Development and Delivery (DPD&D) organization, focusing on biologics biopharmaceutics (monoclonal antibodies, multispecifics, antibody drug conjugates (ADCs), fusion proteins, and other therapeutic protein modalities).  This role will lead scientific strategies and experimental programs on bridging approaches (e.g., IV-to-SC and SC-to-SC), drug delivery platforms, combination products, and targeted delivery.  This individual will apply expertise in pharmacokinetics, biopharmaceutics, and formulation science to advance biologics from early development through clinical phases. Principal Responsibilities: - Design and execute studies to characterize SC absorption and bioavailability of biologics including the development and validation of in vitro-in vivo correlation (IVIVC) tools and models. - Develop intravenous-to-subcutaneous (IV-to-SC) and SC-to-SC bridging strategies to support clinical development and regulatory submissions. - Support biocomparability assessments for Drug Substance (DS) or Drug Product (DP) changes. - Drive Innovation in large-volume, high viscosity, high-concentration, novel formulations and delivery devices to enable high dose SC delivery. - Collaborate with Drug Delivery Systems (DDS) team on combination product development. - Develop in vitro and in silico tools and models to support formulation selection and clinical translation. - Apply pharmacokinetic (PK) modeling to support formulation and drug product presentation decision and bridging strategies. - Advance targeted delivery strategies, including blood-brain barrier (BBB), intratumoral, and other innovative delivery approaches, supported by development of relevant in vitro and in silico models. - Use prior knowledge and predictive tools to define control strategies and design space that are scientifically justified, regulatory-aligned, and patient-focused. - Represent Biopharmaceutics on product development teams and support the biologics portfolio. - Mentor and promote technical excellence across the organization. - Author technical reports, publications, and regulatory submissions. Qualifications: - A minimum of a Ph.D. in Pharmaceutical Sciences or Chemical Engineering, or a PharmD in Pharmacy or a related discipline is required. - A minimum of 3 years of experience in biologics product development is required. - Experience applying PK, PBPK, and other model-informed approaches to support IV-SC, SC-SC bridging strategies and inform formulation and drug product presentation strategies is preferred. - Familiarity with IVIVC or IVIIVC-like approaches to assess the impact of formulation or delivery systems on absorption and exposure is preferred. - Understanding of biologics formulation principles and their relevance to PK and clinical performance is preferred. - Experience with drug-device integration and bridging strategies for combination products is preferred. - Experience with biocomparability assessments is preferred. - Must have excellent verbal and written communication skills. - Must have strong organizational skills. - Must be creative with a strong scientific mindset. - The ability to collaborate effectively with cross-functional teams is required. #LI-Hybrid   Required Skills:     Preferred Skills: Analytical Reasoning, Biochemistry, Biotechnology, Chemistry, Manufacturing, and Control (CMC), Clinical Research and Regulations, Clinical Trial Designs, Coaching, Critical Thinking, Drug Discovery Development, Emerging Technologies, Molecular Diagnostics, Organizing, Pharmacovigilance, Presentation Design, Process Improvements, Productivity Planning, Scientific Research

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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