CIP/SIP CQV Validation Engineer — Biotech Pharma

Veg Group; Juncos (PR); On-site; USD 80,000 - 100,000; Full time

Job summary

A leading services supplier in healthcare is seeking a Validation Specialist for Commissioning, Qualification, and Validation activities related to Cleaning-In-Place systems. Ideal candidates should have a Bachelor’s degree in relevant engineering fields and 7–10 years of experience in biotech or pharmaceutical environments. The role requires knowledge of cleaning validation, automation integration, and familiarity with various systems. This position offers a chance to make a significant difference in healthcare.

Qualifications

• Minimum 7–10 years of experience in CQV within biotech or pharmaceutical manufacturing environments.
• Strong knowledge of cleaning validation, sterilization principles, and automation integration.
• Experience in generating and executing documentation for CQV activities.

Responsibilities

• Planning, coordinating, and executing all CQV activities related to Cleaning-In-Place (CIP) systems.
• Reviewing and approving vendor FAT/SAT protocols.
• Generating and reviewing URS, FAT/SAT, IOQ, and PQ documentation.

Skills

Cleaning validation principles

Bilingual (English / Spanish)

Process validation

Data integrity

Education

Bachelor’s degree in Chemical, Mechanical, or Biochemical Engineering

Tools

DeltaV

SCADA

PLC systems

Job description

A leading services supplier in healthcare is seeking a Validation Specialist for Commissioning, Qualification, and Validation activities related to Cleaning-In-Place systems. Ideal candidates should have a Bachelor’s degree in relevant engineering fields and 7–10 years of experience in biotech or pharmaceutical environments. The role requires knowledge of cleaning validation, automation integration, and familiarity with various systems. This position offers a chance to make a significant difference in healthcare.