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Project Engineer

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Job Reference: JO-1907-64646_1569604601


Project Engineer

This is a 12-month rolling contract position reporting to the Engineering Manager. The successful candidates will plan, design, coordinate, validate and implement high technology equipment and/or processes for the site. He/she will also provide engineering support to ensure high yields and minimize downtime of process equipment prior to implementation into production.


  • Responsible for introducing and validating new equipment and/or complex new process projects from design through completion and in compliance with regulatory requirements.

  • Project management & planning and liaising with other departments affected by these projects. Also reporting project status to management and highlighting areas of concern early.

  • Ensuring all projects are completed to agreed timelines and within budget.

  • Planning and managing equipment implementation to ensure effective utilization of multi departmental resources both internal and external to the company.

  • Assigned work adheres to EHSE requirements.

  • Ensure continual Quality System compliance by adherence to established Client requirements

  • Author and/or review and approval of protocols, technical reports, SOPs, and technical specifications. Compilation of technical documentation for regulatory submissions.

  • Applying cost improvement and LEAN Manufacturing initiatives in projects.

  • Responsible for optimising new processes through process analysis and the application of engineering principles.

  • Manages assignments / project works performed by outside vendors

  • Provide Support to the engineering department when required.

You Demonstrate

  • At least 4- 5 years engineering experience in Pharmaceutical industry in a production environment with Knowledge of process engineering, equipment, automation specification and GMP validation requirements.

  • Bachelor's degree in Process; Chemical; Mechanical; Electrical Engineering or other related discipline.

  • Project Management Qualification desirable

  • Experience of current cGMP requirement of an FDA/HPRA approved facility

  • PC and software proficiency - Microsoft software and Microsoft project

  • Must be good record keeper and data analyser, attention to detail, accuracy and documentation skills

  • Must be a self-starter who can work independently with minimal supervision

  • Strong team player with the ability to work collaboratively and cross functionally

  • A positive mindset of Safety First

  • Travel may be required as part of the role from time to time depending on project needs

Fastnet has a strict confidentiality policy - please be assured that your details will never be forwarded to any third party without your consent.

Fastnet - The Talent Group
'Not Just Placers.........Partners'

The Life Science Specialists

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