Job Title: Commissioning Quality Verification Specialist
Job Description:
This is an exciting opportunity to work on a large-scale project in Dublin, Ireland. As a Commissioning Quality Verification (CQV) Engineer, you will be responsible for ensuring the commissioning readiness of all systems and managing their lifecycle.
The successful candidate will have extensive experience in design and construction projects for biopharmaceutical manufacturing facilities. They will also possess strong leadership and communication skills, with the ability to keep pace with changing business needs.
The role involves working closely with various project groups, including Design, Construction Management, CQV, Automation, Process, SMEs, Operations, Maintenance, and Project Managers. Your primary responsibility will be to ensure that all systems are managed appropriately throughout the project lifecycle.
* Ensure Commissioning Readiness of All Systems.
* Liaise with Project Groups to Ensure Appropriate System Management.
* Lead Execution of CQV Deliverables.
Required Skills and Qualifications:
You should possess the following skills and qualifications:
* Extensive experience in design and construction projects for biopharmaceutical manufacturing facilities.
* Strong leadership and communication skills.
* Ability to keep pace with changing business needs.
* Demonstrated proficiency in communicating and collaborating at various levels.
* Proven success in working well in a team environment.
* Computer skills in Spreadsheets, Word Processing, Visio, and Microsoft Project.
Benefits:
As a member of our team, you can expect:
* A fast-paced and dynamic work environment.
* The opportunity to learn new technology and develop current skills.
* The chance to work on a large-scale project with cutting-edge technology.
Others:
We are looking for candidates who are motivated, flexible, and able to adapt quickly to changing situations. If you are interested in this role, please apply now.