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Quality engineer

Cork
Fastnet - The Talent Group
Quality engineer
Posted: 11 September
Offer description

We are looking for an experienced
Project Engineer
to join our clients engineering team in Cork
.
This position reports to the Capital Project Manager.
This an 18-month Fixed Term Contract.
This is a varied role, and you will be involved in everything from completing feasibility studies to leading commissioning and validation activities at a growing pharmaceutical manufacturing plant.
Key Responsibilities
Project management of the execution of capital engineering projects within the site, following the Project Lifecycle approach.
Support the Operations Engineering Team in controlling uptime of process equipment and optimizing efficiencies both in equipment and process performance.
Improve the operations and reliability of equipment and processes by the successful identification and implementation of continuous improvement initiatives.
Liaise with Internal/External Engineering Personnel and contract maintenance providers in maintaining, troubleshooting and installing/commissioning equipment.
Leadership of equipment commissioning and validation activities as part of capital project execution.
Work closely with cross-functional teams from other departments to deliver the site capital project portfolio.
Prepare feasibility studies and budget management for all assigned capital projects.
Support all major site initiatives and sites core goals.
Prepare Requests for Capital Expenditure (RCE) for site capital projects.
Liaise with Global Engineering as required – eCOPs (engineering communities of practice), Engineering forums, etc.
Responsible for all Engineering contractor management on-site, required to deliver capital projects i.e. ensure safety standards are met, and safe working practices adhered to at all times – RAMS, permit to work, training records, etc.
Qualifications & Experience
Degree in a relevant Engineering subject area– Chemical/Process/Mechanical Engineering preferred.
Strong previous pharmaceutical experience is essential (minimum 7-10 years).
Knowledgeable/competent with executing change control.
Knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry
Demonstrated relevant site experience of one or more of the below:
Cleanroom processing/utilities – HVAC, CIP systems, Purified water generation and distribution systems, Nitrogen, etc.
Nice to have experience
Experience of process engineering, with relevant experience of batch processing, automation, project management, commissioning and validation, equipment reliability and continuous improvement is desirable.
Electrical background – competency with electrical system design & installation (process equipment and site electrical infrastructure), familiar with ATE
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