A leading biopharmaceutical company is seeking a CQV Engineer to support the Commissioning, Qualification, and Validation of utilities, equipment, as systems at its South Dublin facility. This role is a 12-month contract with the possibility of extension.
Interviews and offer can happen this week so get in touch ASAP to discuss further!
Location: Onsite in South Dublin, Ireland (5 days/week).
Contract Duration: 12 months (with possibility of extension).
Work Hours: 40 hours per week.
Start Date: ASAP
Key Responsibilities
Lead commissioning, qualification, and validation (CQV) activities for utilities, new and existing equipment, and systems.
Main focus of validation efforts will be in utilities
Develop, execute, and report on validation protocols (IQ, OQ, PQ).
Review and approve vendor protocols to ensure compliance with project requirements.
Support troubleshooting, deviations, and change control related to equipment validation.
Work closely with cross-functional teams to ensure seamless project execution.
Candidate Requirements
Minimum 3 years of experience in a CQV role within the biopharmaceutical industry.
Strong background in equipment validation.
Strong background in utilities validation.
Experience with computer systems is a plus.
Excellent documentation and communication skills.
Interested? Send your CV to o.titelman@panda-int.com to discuss further!
#J-18808-Ljbffr