CQV Engineer

PE Global (UK); Dublin; On-site; EUR 50,000 - 70,000; Full time

Job summary

A leading biotechnology firm in Dublin is seeking a CQV Engineer to manage commissioning and qualification of equipment and processes. The ideal candidate has over 3 years of experience in engineering with a solid understanding of GMP compliance. This is an initial 12-month contract role, and candidates must possess the correct visa to work in Ireland.

Qualifications

• 3+ years’ experience in Engineering or Commissioning and Qualification Management.
• Extensive knowledge in pharmaceutical/biotech projects preferred.
• Familiar with GMP and regulatory requirements.

Responsibilities

• Owns projects and equipment, drafting and executing protocols.
• Coordinates and supervises all C&Q activities.
• Ensures C&Q schedule is maintained.

Skills

Commissioning and Qualification Management

Communication skills

Leadership skills

Risk-based approach

Technical expertise in biotech

Education

Technical qualification in Engineering

Job description

PE Global is currently recruiting for a CQV Engineer on behalf of a leading biotech company based in Dublin South. This is an initial 12-month contract role.

Overview

• Owns projects, equipment, responsible for document drafting and protocol execution
• Single Use / Formulation / Equipment Commissioning and Qualification (C&Q) engineer for a capital project.
• Ensure the C&Q activities associated with the capital project are completed safely, as per schedule and in compliance with GMP and Quality Requirements.

Responsibilities

• Commissioning & Qualification of Single Use Systems / Formulation Equipment / Process equipment.
• Generation of all C&Q test documents (C&Q Plan/Set to Works/FAT/SAT/IV/FT/C&Q Summary Report
• Provide technical assistance during investigations and system design.
• Coordinates and Supervises all C&Q activities on their systems.
• Ensures the C&Q schedule is maintained.
• Manages Daily C&Q coordination meetings.
• Responsible for Tracking and Reporting of C&Q status and risks/issues.
• Ensures Startup of equipment/utilities is completed in a safe and coordinated manner.
• Assist in the development of User Requirement Specifications (URS’s) and Quality Risk Assessment for Equipment and Automated Systems (QRAES).

Education / Experience

• 3+ years’ experience in Engineering or Commissioning and Qualification Management
• Technical qualification at third level or equivalent in Engineering.
• Extensive knowledge and demonstrated experience managing Commissioning and Qualification for Pharmaceutical / Biotechnology projects preferred
• Knowledge of safety, GMP and environmental regulatory requirements.
• Demonstrated strong Communication and Leadership skills.
• Demonstrated ability to collaborate with senior stakeholders to achieve optimal outcomes.
• Strong understanding of a risk‑based approach to commissioning and qualification within the biotechnology industry
• Familiarity with paperless validation systems.

Interested candidates should submit an updated CV.

Please click the link below to apply, call Kellie on 0214297900 or alternatively send an up to date CV to [e-mail]

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***