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 environmentExperience of delivering engineering projects within a GMP regulated environment, specifically Pharma.
MUST have experience:
Delivering engineering projects within a GMP-regulated pharmaceutical environmentLeading commissioning and qualification (C&Q) activitiesCapital 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 alwaysCompletion of all documentation in compliance with site procedures and GDPPrioritize and scheduling of activities to support business needs and to meet requirements of Master Production SchedulesGenerate 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 Science3+ years’ experience delivering engineering projects in Pharma GMP environmentsInterface at with all site departments, Operations, Maintenance, Facilities, Quality, MSAT, Commissioning/Qualification and Training departments.Strong understanding of cGMP, EHS, and regulatory complianceExperience working in cross-functional, multinational engineering teamsExcellent communication skills (written and verbal)Strong problem-solving and technical aptitude
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