Clean Utilities Engineer
This job does not exist anymore.
Try running a new searchor browse our vacancies.
Or fill in the form below to receive job alerts.
| Job Type | Permanent |
| Area | Sligo, Ireland |
| Sector | Engineering |
| Start Date | |
| Advertiser | Darcy Ainscough-Denton |
| Telephone | +353 1 574 6266 |
| Job Ref | 1003048 |
| Job Views | 303 |
- Description
- Team Horizon is seeking a Clean Utilities Engineer for our global biopharmaceutical client based in Sligo. As Clean Utilities Engineer, you will take ownership for clean utilities (Purified Water, Water for Injection, Clean Steam, High Quality Compressed Air and Nitrogen Distribution) and to work as a team member in line with all safety, regulatory and organizational requirements.
Why you should apply:
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
Provide technical assistance to the manufacturing areas related to the manufacturing process and equipment. These areas are highly dependent on technique, detailed procedures, equipment and controls.
Subject Matter Expert for Clean Utility Engineering from design phase to equipment handover.
Review and approve process flow diagrams (PFDs), specifications, layouts and P&ID’s.
Subject Matter Expert in mechanical, electrical and pneumatic utility systems.
Participate and lead clean utility project implementations.
Lead, promote, participate and supervise the implementation and maintenance of the relevant safety programmes.
Deal with difficult technical problems in a highly technical and regulated Biologics Plant.
Develop and implement changes that will improve equipment performance and consequently product quality.
Review and approve process related commissioning, qualification and validation protocols for completeness and accuracy.
Execute protocols in a timely basis to meet the project schedule requirements.
Cross functional collaboration with Quality, Operations and Engineering functions.
Adheres to and follows all procedures policies and guidelines ensuring compliance with cGMP and ISO/FDA regulations and company policies, procedures and guidelines.
Any other duties as assigned.
What you need to apply:
A relevant third level qualification in an engineering, science or technical discipline.
At least five years of total combined experience in Clean Utility / Equipment or Manufacturing Engineering of a Pharmaceutical and Health Care Organization.
Previous experience in manufacturing processes of biotechnological drugs, parenteral drugs, solutions preparation, fill finish, Lyophilization, sterilization operations preferable.
Experience in clean utilities is essential. Requires total commitment to Quality and maintaining a high standard of work at all times.
Proven ability to work cross-functionally, strong communication skills both verbal and written are required for the execution of this role.
