Validation Engineer

Ardena

Ghent, Belgium
Not specified; benefits: flexible working hours; 3...
On-site
Gmp quality system knowledge
Equipment qualification protocols
Computerized systems validation
Ardena is seeking a Validation Engineer for their Gent location in Belgium, focusing on supporting equipment and computerized systems validation within a pharmaceutical manufacturing environment. The ideal candidate should have experience in GMP compliance, strong technical skills, and the ability to manage multiple projects

Job Summary

  • The Validation Engineer is responsible for day-to-day support regarding equipment issues and implementing the Validation Master Plan.
  • Ardena partners with pharmaceutical companies to turn scientific ideas into real treatments while maintaining the highest quality standards.
  • The role offers a true learning environment with flexible working hours and an attractive remuneration package including 32 days of holiday.

Matching Summary

Match Score: 85

Ardena is seeking a Validation Engineer for their Gent location in Belgium, focusing on supporting equipment and computerized systems validation within a pharmaceutical manufacturing environment. The ideal candidate should have experience in GMP compliance, strong technical skills, and the ability to manage multiple projects.

Salary

Not specified; Benefits: Flexible working hours; 32 days holiday a year; Attractive remuneration package

Skills & Requirements

Must-have

  • GMP quality system knowledge
  • Equipment qualification protocols
  • Computerized systems validation
  • Pharma industry experience
  • Procedure and report drafting

Nice-to-have

  • Solution driven mindset
  • Strong communication skills
  • Continuous improvement focus
  • Project management ability
  • Documentation organization preference

Key Requirements

  • Experience in pharma essential
  • Hands-on laboratory or production experience
  • Willingness to join rotating on-call duty

Work Rights

Not specified

Tailored Resume

Cover Letter