MSAT Validation Engineer — Biopharma Process Excellence

Panda International

Leiden

On-site

EUR 83,000 - 124,000

Full time

14 days+
Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

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.
Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

MSAT Validation Engineer — Process Excellence in GMP
MSAT Validation Engineer — Process Excellence in GMP

Adryan • Leiden

On-site
EUR 45,000 - 60,000
Process Validation Engineer- MSAT
Process Validation Engineer- MSAT

Adryan • Leiden

On-site
EUR 45,000 - 60,000
Engineer MSAT Validation
Engineer MSAT Validation

Panda International • Leiden

On-site
EUR 83,000 - 124,000
Competitive hourly rate
Full-time position
MSAT Process Engineer - Biopharma, Amsterdam (Flexible)
MSAT Process Engineer - Biopharma, Amsterdam (Flexible)

WACKER • Amsterdam

On-site
EUR 60,000 - 85,000
Attractive salary
Holiday allowance
Home-office travel allowance
+2
MSAT Process Engineer
MSAT Process Engineer

Walker Cole International • Hoofddorp

On-site
USD 69,824 - 116,374
GMP Validation Engineer — Biotech CQV Specialist
GMP Validation Engineer — Biotech CQV Specialist

Panda International • Leiden

On-site
EUR 60,000 - 80,000
Senior MSAT Validation & Lifecycle Specialist
Senior MSAT Validation & Lifecycle Specialist

Bristol-Myers Squibb Co • Leiden

Hybrid
EUR 90,000 - 110,000
MSAT Validation & LCM Manager – Cell Therapy (Hybrid)
MSAT Validation & LCM Manager – Cell Therapy (Hybrid)

Bristol-Myers Squibb Co • Leiden

Hybrid
EUR 110,000 - 140,000
Senior MSAT Validation & Lifecycle Lead
Senior MSAT Validation & Lifecycle Lead

Bristol Myers Squibb • Leiden

On-site
EUR 90,000 - 120,000
MSAT - Process Engineer
MSAT - Process Engineer

WACKER • Amsterdam

On-site
EUR 60,000 - 85,000
Attractive salary
Holiday allowance
Home-office travel allowance
+2