Quality Assurance Validation Specialist

Fortil Group

Lazio, Italy
On-site
Iq oq pq qualification approval
Process validation oversight
Gmp sterile environment experience
Fortil Group is seeking a Quality Assurance Validation Specialist for a pharmaceutical project in Lazio, Italy. The ideal candidate should have 1-2 years of experience in quality assurance within a GMP environment, with a strong understanding of process validation and qualification

Job Summary

  • The role involves supervising and approving qualification activities (IQ/OQ/PQ) for manufacturing plants and equipment.
  • Candidates will support process validation activities including critical and sterile processes while collaborating daily with Production, Engineering, and QC teams.
  • Fortil offers a unique opportunity to become a shareholder and participate in personal development initiatives within an international engineering group.

Matching Summary

Match Score: 85

Fortil Group is seeking a Quality Assurance Validation Specialist for a pharmaceutical project in Lazio, Italy. The ideal candidate should have 1-2 years of experience in quality assurance within a GMP environment, with a strong understanding of process validation and qualification.

Skills & Requirements

Must-have

  • IQ OQ PQ qualification approval
  • Process validation oversight
  • GMP sterile environment experience
  • Deviation CAPA management
  • Regulatory audit support

Nice-to-have

  • Cross-functional collaboration skills
  • Risk assessment expertise
  • On-floor production support
  • Continuous improvement mindset

Key Requirements

  • 1-2 years of relevant experience
  • Experience in GMP sterile environments
  • Knowledge of process validation and qualification

Work Rights

Not specified

Tailored Resume

Cover Letter