Senior Regulatory Affairs Scientist

Johnson & Johnson

Raritan, New Jersey, United States
Base: $109,000 to $174,800; bonus: eligible for an...
Hybrid
Master's degree in scientific discipline
3 years regulatory affairs experience
Understanding of drug development process
Johnson & Johnson is seeking a Senior Regulatory Affairs Scientist to join their Innovative Medicine team in a hybrid work environment. The role involves supporting drug development programs and requires a strong understanding of regulatory processes in the pharmaceutical industry

Job Summary

  • This role supports global R&D initiatives by developing treatments and finding cures for complex diseases across multiple therapeutic areas.
  • The position offers a flexible rotational model to gain broad regulatory experience in early-to-late drug development and life-cycle activities.
  • Employees are eligible for competitive compensation including an annual performance bonus, comprehensive benefits, and long-term incentive programs.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Regulatory Affairs Scientist to join their Innovative Medicine team in a hybrid work environment. The role involves supporting drug development programs and requires a strong understanding of regulatory processes in the pharmaceutical industry.

Salary

Base: $109,000 to $174,800; Bonus: Eligible for annual performance-based cash bonus; Benefits: Medical, dental, vision, 401(k), paid time off, parental leave

Skills & Requirements

Must-have

  • Master's degree in scientific discipline
  • 3 years regulatory affairs experience
  • Understanding of drug development process
  • Knowledge of FDA and EMA guidelines
  • Experience in health regulated industry

Nice-to-have

  • Neuroscience therapeutic area experience
  • Life cycle management applications
  • Cross-functional team collaboration
  • Project management skills
  • Proactive issue resolution

Key Requirements

  • Minimum Master's degree required
  • 3 years relevant RA experience with Master's OR 2 years without
  • Prior experience in pharmaceutical or biotech industry
  • Understanding of regulatory submission and approval processes

Work Rights

Not specified

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