Principal Scientist, Pharma Product R&d

Johnson & Johnson Johnson & Johnson · Pharma · Beerse, Antwerp, Belgium

The Principal Scientist, Scientific Integrator Pharmaceutical Product Development & Supply role at Johnson & Johnson is responsible for integrating Drug Product Development activities for synthetic drug candidates. This includes developing and delivering robust clinical and commercial formulations and scalable manufacturing processes, ensuring compliance with scientific, quality, and regulatory standards, and leading cross-functional teams to deliver project milestones within established cost, time, and quality targets. The role acts as the PPDS representative on CMC new product development teams and collaborates with various internal and external partners.

What you'd actually do

  1. Implements the Drug Product development strategy for synthetic drug candidates across all clinical phases including regulatory submissions in major and regional markets, and transition to supply chain operations.
  2. Develops and delivers robust clinical and commercial formulations and scalable manufacturing processes, informed by a deep understanding of compound properties and the Target Product Profile (), to achieve required performance and cost targets.
  3. Acts as matrix leader to drive project delivery through collaboration within PPDS and cross-functional partnership within the CMC teams, CDT (preclinical and clinical) teams, and the commercial organization.
  4. Ensures compliance with applicable scientific, quality and regulatory standards throughout development and transfer activities
  5. Serves as the PPDS representative on the CMC core team, facilitating critical interactions with API and analytical integration partners, supply chain, Quality Assurance, CMC Regulatory Affairs, and external consultants and vendors

Skills

Required

  • Master's degree or PhD in Chemistry, Pharmacy, Biochemical Engineering, Chemical Engineering, or a related field
  • Minimum of three years’ relevant professional experience
  • Scientific and technical competence across drug product development
  • Process scale-up experience
  • Technical transfer experience
  • Leadership in coordinating integrated activities
  • Cross-functional team collaboration
  • Communication skills
  • Decision-making skills
  • Organizational oversight
  • Influencing stakeholders
  • Conflict management
  • Negotiation skills

What the JD emphasized

  • minimum of three years’ relevant professional experience
  • Demonstrated high level of scientific and technical competence
  • Consistent track record in process scale-up
  • Established leadership in coordinating integrated activities
  • Outstanding communication skills
  • Decisive, with the ability to make prompt, well-reasoned decisions
  • Ability to influence stakeholders and secure alignment in a matrix environment without direct line authority.
  • Excellent written and oral communication skills