QA Specialist

3 days ago


Dublin, Ireland PE Global (UK) Full time

PE Global is recruiting for a CQV Engineer on behalf of our biopharmaceutical client in Dublin. This is an initial 12-month contract role.

Duties of the role:

- Be the engineering lead for CIP project (long-term project) and work together with Capital Projects department.
- Ensure schedule adherence and project deliverables are achieved, working closely with OpU, Program Leads and Stakeholders, displaying the ability to meet challenging timelines within the constraints of Plan of Record, through a pro-active mindset and demonstrated innovative thinking approach to work around these, and other constraints.
- Strong commissioning and validation experience for active involvement in the C&Q phases and Delta V, with on-the-floor presence, bringing the different teams along.
- Develop and maintain relationships, systems, workstreams with your corresponding Capital Portfolio owners and all the different Operational Units.
- Experienced in managing capital and cashflow project, and work with capital/PM teams to manage cashflow and capital.
- Mindset of flexibility and fluidity to work and lead different work cells through challenging and varied project types in an ever-changing landscape.
- Manage, when applicable, the relationship with the A&E/Construction Management/external vendors teams through respective phases of a project.
- Excellent planning and project management skills.
- Effective motivator and communicator, a demonstrated ability to effectively influence at all levels, with a history of creating good working relationships with all departments and ability to see from all perspectives, from the OpU to other engineering departments and to other non-engineering disciplines.
- Embed a safety culture within the engineering team during all phases of the project lifecycle.
- Capable of working independently, in a well-structured manner while maintaining good communication with stakeholders & vendors.

Education & Experience:

- Degree in an engineering or similar discipline.
- Minimum of 4 years engineering experience in biotechnology or pharmaceutical GMP manufacturing environment.

Interested candidates should submit an updated CV.

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