Project Engineer III
Description
Project Engineer III
Team Horizon is seeking a Project Engineer III (initial 12-month contract) for our client in Sligo who are a leader in the global biopharmaceutical industry.
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:
• To provide Engineering services to the plant, in order to maximise the availability of all Site Process Equipment and Utilities.
• To manage capital engineering projects within site following the client’s Project Lifecycle approach (typical project value range: anything up to €5 million).
• To support the engineering teams in controlling uptime of process equipment and optimizing efficiencies both in equipment and process performance.
• To support the Engineering team with the emphasis on continual operational improvements.
• To provide process engineering support and technical trouble shooting within the site.
• To improve the operations and reliability of equipment and processes by the successful identification and implementation of continuous improvement initiatives.
• To manage the execution of projects within the engineering group including specific Process Safety Projects.
• To support the provision of process safety initiatives to the site.
• To liaise with Production to ensure equipment performance is maximized.
• To liaise with Internal/External Engineering Personnel and contract maintenance providers in maintaining, troubleshooting and installing/commissioning equipment.
• To provide engineering support and technical trouble shooting to all site operations and reliability of equipment and processes by the successful identification and implementation of continuous improvement initiatives.
• Leadership of process equipment commissioning and validation activities.
• Identification and project management of continuous improvement projects.
• Work closely with all site functions and other departments to deliver these continuous improvement projects.
• Preparation of feasibility studies and budget management for all assigned projects.
• Management and negotiation of external contracts and contractors.
• Support all major site initiatives and sites core goals.
• Any other duties as assigned.
What you need to apply:
Essential
• Degree in a relevant Engineering Discipline (Mechanical/Chemical/Process).
• 5 years + strong site experience in API Manufacturing / OSD Manufacturing / BioPharm but will consider more junior (3 years) if they have relevant project site experience.
• Proven track record in delivering Capital Projects – new equipment, utilities, facilities, etc.
• Good knowledge of change control and C&Q processes/execution.
• Must have demonstrated relevant site experience of one or more of the below.
• API process equipment trains (reactors, filter dryers, pumps, process pipework, milling, containment technology – gloveboxes, downflow booths, etc.).
• Drug Product equipment (tablet press, roller compaction, tablet coater, material.
• Handling – post hoists, blenders, milling – Quadro Comils, etc.).
• Cleanroom processing/utilities – HVAC, CIP systems, Purified water generation and distribution systems, etc.
• Knowledgeable/competent with executing change control.
• Experience in process engineering, with relevant experience of batch processing, automation, project management, commissioning and validation, equipment reliability, and continuous improvement.
• Working knowledge of distributed control systems, such as Delta V.
• This is a hand-on role requiring a logical and structured approach to resolving day to day engineering issues typical of a live manufacturing environment.
• Knowledge of cGMP and regulatory requirements relating to the Healthcare industry is required.
• Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality requirements.
Desirable
• Trackwise change control system experience.
• Electrical background – competency with electrical system design & installation (process equipment and site electrical infrastructure), familiar with ATEX regulations and requirements.