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Role: Project Engineer

Contract: 12 months

Location: Little Island, Cork

The Role:

At Hays, we are working with a leading Pharmaceutical company in Cork that is hiring a Project Engineer. As part of the Global Engineering & Technology Team, this contract position is responsible for all activities required to support the successful delivery of new engineering projects within the company.

GENERAL ACTIVITIES:

•Lead the delivery of Engineering projects on time, on budget & in accordance with all project & business goals.

•Scope new Engineering projects & secure capital approval

•Lead, support and participate in commissioning and qualification activities

•Participate in and lead Cross-Functional teams as necessary.

•Updating & influencing management and project stakeholders.

•Troubleshooting of process or equipment issues

•Coordination of project interfaces with other projects and departments

•Coordination of and interfaces with third parties (suppliers, customers, service providers, etc.)

•Coordination of project documentation and or P&IDs

•Project Cost Management (estimation, forecasting, tracking, updating)

•Project Scheduling (creation, tracking & reporting)

•Project progress reporting & Risk Management

•Constructability & Maintainability/Operability studies

•Project Resource Management

•Reviewing current condition of systems (structural, E&I as well as safety, permitting and documentation)

•Organization & coordination of project meetings

•Investigating and resolving deviations raised within the Engineering Department

•Provide process and equipment related training as required.

•Completion of assigned tasks to support manufacture of quality medicines in accordance with cGMP and EHS requirements.

•Retrospective project performance review versus project goals and lessons learned.

SCOPE OF 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 at all times

•Completion of all documentation in compliance with site procedures and GDP

•Prioritize and scheduling activities to support business needs and to meet the 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 through Operations, Quality Validation, MSAT, Facilities and other support functions.

•Travel to other J&J 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.

QUALIFICATIONS AND EXPERIENCE:

ESSENTIAL:

•Third level qualification in Engineering or Science.

•3+ years’ experience working in a Pharmaceutical environment

•Experience of delivering engineering projects within a GMP regulated environment, specifically Pharma.

DESIRABLE:

•Qualification in Project Management

•6-Sigma or similar problem-solving/decision-making methodology training

•Experience of working within an Engineering team in a multinational corporate environment.

•Experience of Microsoft Word, Excel and Outlook