Specialist Quality Assurance - Qa Npd

Johnson & Johnson

Leiden, Netherlands
Base: 53,500.00 - 85,445.00; bonus/equity: not spe...
Not specified
Qa support for new product introduction
Quality oversight for technology transfer
Review quality investigations and non-conformances
Johnson & Johnson is seeking a Specialist Quality Assurance (QA) professional for their Leiden, Netherlands location, focusing on quality oversight for new product introductions and lifecycle transitions. The ideal candidate will have experience in a GMP-regulated environment and possess strong problem-solving and collaboration skills

Job Summary

  • Provides QA support to the introduction, launch, and lifecycle transition of new products to the Leiden manufacturing site.
  • Assesses and reviews Quality Investigations and non-conformances, supports investigation teams, ensures robust root cause analysis, and determines product impact and disposition based on GMP and compliance considerations.
  • Participates as Core Team Member in New Product Introduction projects and provides Quality oversight to the introduction of New Products to the site, including CTM, PPQ, and commercial readiness for routine manufacturing.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Specialist Quality Assurance (QA) professional for their Leiden, Netherlands location, focusing on quality oversight for new product introductions and lifecycle transitions. The ideal candidate will have experience in a GMP-regulated environment and possess strong problem-solving and collaboration skills.

Salary

Base: 53,500.00 - 85,445.00; Bonus/Equity: Not specified; Benefits: 8% holiday allowance

Skills & Requirements

Must-have

  • QA support for new product introduction
  • Quality oversight for technology transfer
  • Review quality investigations and non-conformances
  • Participate in risk assessments
  • GMP compliance in regulated environment

Nice-to-have

  • Foster strong quality culture
  • Customer-oriented attitude
  • Negotiation skills
  • Influence without formal authority

Key Requirements

  • Bachelor's degree or higher in Biochemistry, Biology, Pharmaceutical degree or relevant education
  • BSc 6 years or MSc 4 years of experience in a GMP regulated environment
  • Proficiency in English
  • Knowledge of cGMP/ICH/FDA/EMA guidelines

Work Rights

Not specified

Tailored Resume

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