We are currently recruiting for an exciting opportunity within a pharmaceutical organization based in Carlow. This is an excellent position for anyone looking to join a leading multinational that excels in its field.
Job Description
This role involves reviewing and following up on technical documentation from the early design phase to ensure alignment with GMP and CQV requirements. Additionally, you will investigate and resolve technical issues with assistance from engineers and/or suppliers.
Required Skills and Qualifications
* Strong documentation and GDP awareness is essential for this position.
* You should have a minimum of 5 years post-academic E&I engineer experience in a relevant industry with experience of construction & start-up.
* Excellent communication, presentation, and organizational skills are required.
Benefits
This position offers opportunities for growth and development within a leading multinational. You will work closely with CQV engineers and be responsible for coordinating CQV activities and reporting to the company and clients.
Others
You will also be responsible for final handover reports to client users and managing contractors and vendors. If interested in this posting, please feel free to contact us for further information.