Senior Project Engineer

Role: Senior Project EngineerLocation: Little Island, Cork,IRL ,T45 P663Duration: 12 monthsBack again for 2x Senior Project Engineers for Little Island site, onsite role.They need to have a relevant degree (chemical, process engineering) AND a minimum of 5 years in a Project Engineering role (not C&Q or similar) from an API (active pharmaceutical ingredient) environment. These are non-negotiable.Individuals need to be able to be hands-on, proactive and able to engage with stakeholders.MUST have experience:Relevant degree (chemical, process engineering) AND a minimum of 5 years in a Project Engineering role (not C&Q or similar) from an API (active pharmaceutical ingredient) environment.Description:As part of the Engineering Project Delivery Team, this contract position is responsible for all activities required to support project scoping, commissioning, qualification, validation, and start-up operations at the Innovative Medicine site.These activities include but are not limited to:Key Responsibilities:Lead engineering projects from scoping to commissioning, qualification, validation, and start-up, ensuring projects are on time, on budget, and meet Safety & Quality goals.Scope new projects and secure capital approval; perform cost estimation, scheduling, tracking, forecasting, and progress reporting.Coordinate cross-functional teams, specialist departments, and third-party stakeholders for smooth project execution.Troubleshoot and resolve process-specific equipment issues, support plant investigations and deviations.Conduct constructability, maintainability, and operability studies; assess system conditions (structural, E&I, safety, permitting, documentation).Generate, review, and maintain engineering and project documentation in compliance with cGMP, EHS, and site procedures.Lead, train, and support team members, fostering continuous improvement, collaboration, and open communication.Participate in or lead cross-functional project teams, supporting site goals and ongoing operational studies.Support external site visits and travel as required for project-related activities.Perform retrospective project performance reviews and implement lessons learned.Key requirements:Education & ExperienceRelevant engineering degree or equivalent experience.Proven experience in engineering project delivery, including commissioning, qualification, validation, and start-up.Experience in cGMP-regulated pharmaceutical or biotech manufacturing environments.Experience coordinating cross-functional teams and external stakeholders.Technical SkillsStrong project management skills: scheduling, budgeting, cost estimation, reporting, and risk management.Experience with process equipment troubleshooting and resolution.Knowledge of structural, E&I, safety, and regulatory systems.Familiarity with documentation compliance (cGMP, GDP, EHS, Change Management Procedures).Leadership & Interpersonal SkillsAbility to lead cross-functional teams and foster collaboration.Strong communication and coordination skills with internal and external stakeholders.Initiative, motivation, and ability to drive continuous improvement.Compliance & SafetyCommitment to safety, quality, and regulatory compliance.Ability to investigate and resolve deviations effectively.OtherWillingness to travel to other sites as needed.Strong organizational skills and attention to detail