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Our client, a leading pharmaceutical company based in Dublin, is seeking a highly experienced Project Engineer for a contract role. This position will focus on a variety of key projects within the pharmaceutical manufacturing environment, including warehouse upgrades, process wastewater system upgrades, and bulk manufacturing plant improvements. The successful candidate will be responsible for leading, coordinating, and overseeing the full project lifecycle, ensuring on-time delivery, within budget, and meeting all regulatory and compliance requirements.
Responsibilities:
* Warehouse Upgrades: Oversee HVAC installation, temperature controls, and insulation works.
* Process Wastewater System: Manage the upgrade of the Dissolved Air Flotation (DAF) system.
* Bulk Manufacturing Plant: Lead the upgrade of a bulk manufacturing plant including the installation of a new process vessel and control systems.
* Manage project schedules, resources, and budgets to ensure timely and cost-effective completion.
* Ensure all engineering and technical documentation is accurate and up to date.
* Lead the execution of the full lifecycle of commissioning, qualification, and validation (CQV) documents including URS, VMP, FAT, SAT, IOQ, PQ, and other related documents.
* Collaborate with internal and external stakeholders to ensure seamless execution of the projects.
* Review project designs and engineering plans, making recommendations for improvements as needed.
* Implement quality assurance and regulatory compliance throughout all project phases.
* Ensure all safety and environmental regulations are adhered to during the execution of the projects.
* Regularly update the management team on project progress, challenges, and budget status.
Requirements:
* Minimum of 10 years of experience as a Project Engineer in the pharmaceutical industry or a similar regulated environment.
* Extensive experience with managing and controlling project budgets.
* Proficiency in writing, executing, and managing the complete lifecycle of CQV documents (URS, VMP, FAT, SAT, IOQ, PQ, etc.).
* Strong knowledge of pharmaceutical engineering systems including HVAC, process wastewater systems (Dissolved Air Flotation), and manufacturing plant upgrades.
* Familiarity with automation and control systems integration.
* Ability to manage multiple projects simultaneously and effectively prioritize tasks.
* Solid understanding of GMP (Good Manufacturing Practices) and FDA/EU regulations.
* Excellent communication and interpersonal skills, with the ability to lead and influence cross-functional teams.
* Strong problem-solving and decision-making abilities.
* Relevant engineering degree (e.g., Mechanical, Electrical, Chemical, or Process Engineering).
* Experience with project management software and documentation tools.
Seniority level
* Seniority level
Associate
Employment type
* Employment type
Full-time
Job function
* Job function
Engineering, Project Management, and Manufacturing
* Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Manufacturing
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