12 month contract for an experienced CQV Engineer with knowledge of upstream equipment and bioreactors €55-€60 per hour - Leinster.

The Position

As a key member of the site CQV project team you will be involved in leading and supporting all aspects of downstream commissioning and validation for the site. This is a challenging position and will require flexibility and creative problem solving.

• Working on a team of experienced professionals; engineers and senior specialists across the site. You will work closely within this group and liaise with on-site teams to support the operational readiness plan from a CQV perspective.
• Be involved with the detailed design of validation solutions for the site around equipment implementation and networking.
• Be a go-to expert on bioreactors, single-use equipment.
• Support FAT's and complete SAT's, IQ and OQ Protocols.
• You will support the resolution of deviations; running investigations across equipment and process deviations, system failures and under-performance ensuring root cause analysis is carried out, a solution is delivered, and corrective actions are implemented across systems and equipment.

The Person

• All applications must have a Degree in Engineering with a minimum of 5 years' experience within a project-based environment.
• The right person will have experience within a highly regulated GMP manufacturing operation - Pharmaceutical or Bio-tech.
• A strong portfolio of CQV work is required and proven skill in this area.
• Flexible approach to work and a positive attitude will be a good fit with the team dynamic
• Be collaborative in your approach to work and be an effective communicator.
• Autonomous with ability to work on your own initiative.

The Benefits

• Competitive hourly rate on offer

To discover more about this opportunity, apply now or contact Aisling Clements at HRM on +353 87 7521041 for a confidential discussion.