CQV Engineer - Excellent Daily Rates - Long Term Contract

Optimus Search; Ballysadare; On-site; EUR 50,000 - 70,000; Full time

Job summary

A leading recruitment agency is looking for a CQV Engineer for a biopharma project in Ballysadare, Ireland. The role involves generating and executing qualification protocols and managing technical documentation within a collaborative team. Ideal candidates will have strong experience in CQV and a hands-on background with bioreactors and clean utilities. This is an on-site position requiring availability 5 days a week, offering an opportunity to contribute to significant project milestones.

Benefits

High-profile biotech project

Collaborative work environment

Opportunity for key project milestones

Qualifications

• Strong CQV experience within biopharma/biotech environments.
• Hands-on background with bioreactors and clean utilities.
• Ability to produce high-quality qualification documentation.
• Effective communicator for vendor and client interactions.
• Must be available for on-site work, 5 days per week.

Responsibilities

• Generate and execute IOQ protocols.
• Prepare and manage technical documentation.
• Interface with vendors and client representatives.
• Support qualification activities within scope.

Skills

CQV experience

Effective communication

Hands-on experience with bioreactors

Knowledge of clean utilities

Job description

Contract CQV Engineer – Bioreactors & Clean Utilities

📍 Location: Ballysadare (Fully On-Site, 5 days/week)

📅 Contract: Ongoing – Immediate Start

We are seeking CQV Engineers to join a growing project team in Ballysadare, supporting bioreactors and clean utilities (WFI, clean steam, etc.). With two CQV engineers already on-site, we are scaling up the team to meet project demands. Our client is a brilliant US company who have opened a new office and are looking to rapidly expand.

Role Responsibilities

• Generate and execute IOQ protocols
• Prepare and manage technical documentation
• Interface with vendors and client representatives
• Support qualification activities within scope (no troubleshooting required at this stage)

Requirements

• Strong CQV experience within biopharma/biotech environments
• Hands‑on background with bioreactors and clean utilities
• Ability to produce high-quality qualification documentation
• Effective communicator for vendor and client interactions
• Must be available for on‑site work, 5 days per week

Why Join?

• Be part of a high-profile biotech project
• Work with an established CQV team on critical systems
• Opportunity to deliver key project milestones in a collaborative environment

Please send your CV ASAP to be considered. Optimus Search have multiple CQV roles all over Europe and the world so get in touch if you are looking or need help in finding freelance staff.