Role: Senior Project Engineer
Location: Little Island, Cork, IRL, T45 P663
Duration: 12 months
Fully onsite position.
Required:
* Third level qualification in Engineering or Science.
* 3+ years' experience working in pharmaceutical environment
* Experience of delivering engineering projects within a GMP regulated environment, specifically Pharma.
MUST have experience:
* Delivering engineering projects within a GMP-regulated pharmaceutical environment
* Leading commissioning and qualification (C&Q) activities
* Capital project scoping, cost control, scheduling, and risk management
Description:
The Engineering Project Delivery Engineer is responsible for supporting the successful execution of engineering projects within a regulated pharmaceutical manufacturing environment. This role focuses on end-to-end project delivery, ensuring projects are completed safely, compliantly, on time, and within budget while supporting the manufacture of high-quality medicines in accordance with cGMP and EHS requirements.
Key responsibilities:
* Responsible and accountable for assuring the safe accomplishment of job activities, in compliance with corporate and cGMP/EHS regulatory requirements.
* Carry out routine and non-routine tasks delegated by the Manager according to appropriate procedures, values, and standards.
* Compliance with Engineering and general site procedures always
* Completion of all documentation in compliance with site procedures and GDP
* Prioritize and scheduling of activities to support business needs and to meet requirements of Master Production Schedules
* Generate and assist with generation, review, and revision of Engineering documentation, as necessary.
* Ensure that personal training requirements are completed in compliance with site procedures.
* Support ongoing studies by Operations, Quality Validation, MSAT, Facilities and other support functions.
* Travel to other sites and other external sites for business related activities as required (5%)
* Lead by example and strive to perform to high standards at all times.
Key requirements:
* Degree-qualified in Engineering or Science
* 3+ years' experience delivering engineering projects in Pharma GMP environments
* Interface at with all site departments, Operations, Maintenance, Facilities, Quality, MSAT, Commissioning/Qualification and Training departments.
* Strong understanding of cGMP, EHS, and regulatory compliance
* Experience working in cross-functional, multinational engineering teams
* Excellent communication skills (written and verbal)
* Strong problem-solving and technical aptitude