Key Responsibilities:
Project Development & Execution
Manage the full lifecycle of projects from planning to execution, including change control, and coordination of both internal and external teams.
Ensure projects are completed on time, within budget, and in line with all safety and regulatory requirements.
Process & Equipment Reviews
Conduct thorough reviews of processes and equipment, preparing detailed technical reports and recommending improvements for quality enhancement and cost reduction.
Specifications & Design
Develop comprehensive user requirement specifications, technical specifications, and design specifications for new or upgraded equipment, ensuring optimal design concepts and technology selection.
Equipment Qualification
Plan and execute equipment qualification protocols (IQ/OQ) to ensure full compliance and operational readiness.
Cross-Functional Collaboration
Work closely with departments such as operations, maintenance, quality assurance, and EHS to minimise disruptions to ongoing production while meeting project goals.
Compliance & Safety
Observe and adhere to all safety procedures and actively identify opportunities for improving safety practices, reducing incidents or near-misses.
Reporting & Continuous Improvement
Provide regular updates on project progress and challenges, ensuring all issues are addressed according to established escalation processes.
Travel & Equipment Selection
Travel as required for equipment selection and participation in Factory Acceptance Tests (FATs), ensuring that chosen equipment meets all necessary specifications.
Requirements:
- Bachelors Degree in Engineering or equivalent combination of education and work experiences required.
- 3-5 years related experience and nor training; or equivalent combination of education and experience.
- Experience in pharmaceutical manufacturing and packaging equipment and/or pharmaceutical processing equipment design, evaluation, and specification is an advantage.
- Detailed understanding of P&IDs, process flow diagrams, and all related pharmaceutical commissioning and qualification documentation.
- Experience working with pharmaceutical processing technologies and good understanding of 2ICFR cGMP documentation and electronic systems requirements.
- Demonstrated experience applying sound engineering principals and critical reasoning to troubleshoot complex process and engineering challenges.
- Proficiency of computer skills with Microsoft Word, Excel, Outlook, CAD.
Why Dublin?
Dublin is a city known for its welcoming community, vibrant cultural scene, and high quality of life. Enjoy a mix of urban energy and beautiful natural surroundings, with access to excellent public services, recreational spaces, and a thriving economy.
This role offers an exciting opportunity for an experienced Project Engineer who is eager to make an impact. If you’re passionate about engineering, project management, and working in a fast-paced environment, apply today to join this dynamic team.