Engineer Msat Lm Validation

Johnson & Johnson MedTech

Leiden, South Holland, Netherlands
Base: 44,700.00 - 80,300.00 eur annually including...
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Process validation of pharmaceutical equipment
Good manufacturing practices (gmp) compliance
Data integrity principles adherence
** Johnson & Johnson MedTech is seeking a Validation Engineer for its Manufacturing Science & Technology (MSAT) team in Leiden, Netherlands. The role focuses on the validation of biotherapeutic drug substances and requires a strong foundation in GMP and validation processes within the pharmaceutical industry. **

Job Summary

  • The Manufacturing Science & Technology (MSAT) department is the leading partner in supporting process validation and deploying sophisticated technologies to enable the best value for patients.
  • The Validation Engineer will assess, plan, and coordinate execution of SPV activities and act as a subject matter expert for validation categories.
  • Johnson & Johnson provides an inclusive work environment respecting diversity and dignity, committed to innovation in healthcare solutions.

Matching Summary

Match Score: 75

** Johnson & Johnson MedTech is seeking a Validation Engineer for its Manufacturing Science & Technology (MSAT) team in Leiden, Netherlands. The role focuses on the validation of biotherapeutic drug substances and requires a strong foundation in GMP and validation processes within the pharmaceutical industry. **

Salary

Base: 44,700.00 - 80,300.00 EUR annually including 8% holiday allowance; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Process validation of pharmaceutical equipment
  • Good Manufacturing Practices (GMP) compliance
  • Data integrity principles adherence
  • Risk management and root cause problem solving
  • Technical product ownership in manufacturing
  • Support audits and inspections

Nice-to-have

  • Experience with mixing validation and sterilization
  • 6-Sigma/Lean continuous improvement methodology
  • Effective communication and documentation skills
  • Mentoring and training team members
  • Knowledge of regulatory guidelines (FDA, EMEA, ICH)

Key Requirements

  • Relevant MS/MBA or bachelor’s degree with experience
  • 0-2 years relevant pharmaceutical or academic experience
  • English proficiency required; Dutch is a plus

Work Rights

Not specified

Tailored Resume

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