A leading engineering group is seeking a Validation Specialist focusing on Cleaning-In-Place (CIP) systems. This role requires expertise in commissioning, qualification, and validation within a biotech setting, ensuring compliance with industry standards. Key responsibilities include reviewing protocols, executing testing, and collaborating with engineering and QA teams. The ideal candidate has a Bachelor's degree in Engineering and 7–10 years of relevant experience, is bilingual, and is ready to contribute to transformative projects in healthcare technology.
Qualifications
Minimum 7–10 years of experience in CQV within biotech or pharmaceutical manufacturing environments.
Experience in generating and executing documentation for CQV activities.
Proficiency in reviewing P&IDs, piping isometrics, and functional design specifications.
Responsibilities
Plan, coordinate, and execute all Commissioning, Qualification, and Validation (CQV) activities.
Review and approve vendor FAT/SAT protocols for CIP/SIP equipment.
Collaborate with Process Engineers and QA for successful integration of CIP/SIP operations.
Skills
Cleaning validation
Sterilization principles
Automation integration
Bilingual (English/Spanish)
Education
Bachelor’s degree in Chemical, Mechanical, or Biochemical Engineering
Tools
DeltaV
SCADA
PLC systems
Job description
A leading engineering group is seeking a Validation Specialist focusing on Cleaning-In-Place (CIP) systems. This role requires expertise in commissioning, qualification, and validation within a biotech setting, ensuring compliance with industry standards. Key responsibilities include reviewing protocols, executing testing, and collaborating with engineering and QA teams. The ideal candidate has a Bachelor's degree in Engineering and 7–10 years of relevant experience, is bilingual, and is ready to contribute to transformative projects in healthcare technology.