CQV Engineer

About the Position

We are seeking a CQV Engineer for a 9-month contract in Dublin to join Pfizer's DS2 Project, focusing on commissioning and qualification of process equipment.

Responsibilities

• Perform shakedown and commissioning and qualification of systems.
• Participate in construction system completion walkdowns.
• Generate CQV documents at project level and for specific equipment/systems.
• Liaise with Quality, Engineering, and CQV to align on Critical parameters and document content.
• Track and confirm closure of action items identified from walkdowns, FAT, HAZOP, Design Qualification, and other reviews.
• Maintain a strong interface with the Automation and Engineering teams to ensure that the information flow meets the needs of the Automation and Engineering teams, resolving issues as they arise.

Requirements

• B.Sc. /B.Eng. degree in engineering discipline, with particular emphasis on mechanical or process engineering.
• Minimum of 4 years’ experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment.
• Demonstrated ability to work on own initiative and proactively respond to business needs.
• Excellent interpersonal and communication skills.
• Familiar with Delta-V & Navisworks is an advantage.

We Offer

• Opportunity to work on a large-scale Cell Culture facility project.
• Collaborate with a leading pharmaceutical company, Pfizer.
• Competitive contract terms.

About the Company

Pfizer is a global leader in biopharmaceuticals, vaccines, and consumer healthcare products. The DS2 Project is a significant initiative to double existing site capacity to meet forecasted demand of licensed and pipeline products.

Application

Interested candidates are encouraged to apply now for this exciting opportunity to be part of a critical project at Pfizer.