A leading services supplier in Barceloneta is seeking a Validation Specialist to coordinate and execute all Commissioning, Qualification, and Validation activities for Cleaning-In-Place systems. Candidates should have a Bachelor’s degree in engineering and at least 7–10 years of experience in CQV within biotech or pharmaceutical sectors. Bilingual proficiency in English and Spanish is required, along with strong knowledge of cleaning validation and compliance with FDA/EMA standards. This is a unique opportunity to contribute to improving healthcare outcomes.
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 and functional design specifications.
Responsibilities
Plan and coordinate all Commissioning, Qualification, and Validation activities.
Generate and review URS, FAT/SAT, IOQ, and PQ documentation.
Collaborate with Process Engineers and QA to ensure integration of CIP/SIP operations.
Skills
Cleaning validation
Sterilization principles
Project management
Data integrity
Bilingual (English / Spanish)
Education
Bachelor’s degree in Chemical, Mechanical, or Biochemical Engineering
Tools
DeltaV
SCADA
PLC systems
Kneat
ValGenesis
Job description
A leading services supplier in Barceloneta is seeking a Validation Specialist to coordinate and execute all Commissioning, Qualification, and Validation activities for Cleaning-In-Place systems. Candidates should have a Bachelor’s degree in engineering and at least 7–10 years of experience in CQV within biotech or pharmaceutical sectors. Bilingual proficiency in English and Spanish is required, along with strong knowledge of cleaning validation and compliance with FDA/EMA standards. This is a unique opportunity to contribute to improving healthcare outcomes.