Senior Associate, Quality Systems Risk Management

J&J FAMILY OF COMPANIES

Leiden, South Holland, Netherlands
Base: eur 64,000 to eur 103,040 annually; bonus/eq...
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Bachelor's degree in life sciences
5 years fda/ema regulated experience
Gmp and quality systems knowledge
** Johnson & Johnson is seeking a Senior Associate in Quality Systems Risk Management, responsible for overseeing quality systems with an emphasis on risk management for clinical trial supplies. The role requires a strong background in GMP, quality governance, and the ability to collaborate with cross-functional teams in a regulated environment. **

Job Summary

  • The role ensures compliance with GMP, quality, regulatory, and internal compliance requirements while supporting clinical trial supplies.
  • Candidates will leverage digital and AI-enabled tools to support trend analysis, risk identification, and data review.
  • This position offers exposure to multiple Quality Centers of Excellence including NC/CAPA, Change Control, and Audits.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Senior Associate in Quality Systems Risk Management, responsible for overseeing quality systems with an emphasis on risk management for clinical trial supplies. The role requires a strong background in GMP, quality governance, and the ability to collaborate with cross-functional teams in a regulated environment. **

Salary

Base: EUR 64,000 to EUR 103,040 annually; Bonus/Equity: Not specified; Benefits: 8% holiday allowance

Skills & Requirements

Must-have

  • Bachelor's degree in Life Sciences
  • 5 years FDA/EMA regulated experience
  • GMP and quality systems knowledge
  • Risk management and CAPA processes
  • Digital and AI-enabled tools familiarity

Nice-to-have

  • Experience with COMET or SUMMIT systems
  • Data-driven quality environment background
  • Matrix cross-functional global collaboration
  • R&D experience in clinical manufacturing
  • Strong analytical problem-solving skills

Key Requirements

  • Bachelor's degree in Life Sciences
  • Minimum 5 years pharmaceutical/biotech experience
  • Knowledge of FDA and EMA regulations
  • Proficiency in GMP and quality governance

Work Rights

Not specified

Tailored Resume

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