Sr Validation Scientist

• Commissioning and qualification of drug substance equipment such as tanks, bioreactors, computerized systems and analytical equipment, facilities, and utilities.
  
• Read a P and ID drawing.
  
• C and Q plan systems URS, Risk Assessments, and vendors documentation.
  
• Elaborate, handling and execute a testing protocol including the resolution of deviations.
  
• Handle a GMP document.
  
• Interact with system vendors during preparatory C and Q activities
  
• Participate when a problem resolution requires C and Q team members provide guidance
  

Requirements

• Doctorate or Masters degree and 3 years of directly related experience or Bachelors degree and 5 years of directly related experience or Associates degree and 10 years of directly related experience
  
• Bilingual (Spanish/English)(Written/Spoken)
  
• Computer Skills
  
• Technical Writing
• Advanced validation knowledge (equipment qualification, cleaning, sterilization).