Ingenieur Qualifizierung / Validierung Pharmaanlagen (m/w/d)
On-site
Core
Planning, coordinating, documenting, and implementing qualification of production equipment and cleanrooms, along with sterilization validations in compliance with GMP regulations.
Role type
Validation Engineer (Pharmaceutical Manufacturing)
Builds
Qualified production equipment, cleanrooms, and validated sterilization processes for pharmaceutical products.
Domain
Pharmaceutical manufacturing / GMP compliance
Required skills
GMP regulations knowledge, risk analysis, root cause analysis, CAPA implementation, change control management, SOP development, cleanroom measurement, training delivery
Preferred skills
Analytical thinking, structured work approach, initiative, teamwork
Technologies
GMP, CAPA, Change Control, SOPs, Cleanroom measurement tools
