MSAT Validation Engineer — Biopharma Process Excellence

Panda International

Leiden

On-site

EUR 83,000 - 124,000

Full time

14 days+

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Benefits offered by this job

Competitive hourly rate
Full-time position

Job summary

A leading recruitment firm in biotechnology is seeking a Recruitment Consultant to support technical operations leaders in building high-performing biopharma teams. This mid-senior level position focuses on validation processes and ensuring compliance in a manufacturing science environment. The ideal candidate holds a Bachelor’s degree and has a minimum of 4 years in the (bio)pharmaceutical industry. Strong skills in writing validation protocols and knowledge of regulatory standards are essential. Join this dynamic team in Leiden and drive improvements in patient care.

Qualifications

  • Minimum of 4 years of relevant experience in the (bio)pharmaceutical industry.
  • Experience in cleaning validation, mixing validation, sterilization qualification, or holding time studies.
  • Strong stakeholder management and communication skills.

Responsibilities

  • Drive process improvements and new technology deployment.
  • Plan and execute validation activities while maintaining compliance.
  • Ensure audit readiness through rigorous documentation.

Skills

Writing and reviewing validation protocols/reports
Knowledge of regulatory requirements (FDA, EMA, ICH)
Understanding of risk management and root-cause problem solving

Education

Bachelor’s degree in a Science, Engineering, or Technical subject

Tools

6-Sigma/Lean methodologies

Job description

A leading recruitment firm in biotechnology is seeking a Recruitment Consultant to support technical operations leaders in building high-performing biopharma teams. This mid-senior level position focuses on validation processes and ensuring compliance in a manufacturing science environment. The ideal candidate holds a Bachelor’s degree and has a minimum of 4 years in the (bio)pharmaceutical industry. Strong skills in writing validation protocols and knowledge of regulatory standards are essential. Join this dynamic team in Leiden and drive improvements in patient care.
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