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Electrical and instrumentation lead

Athlone
Life Science Recruitment Ltd
Posted: 12h ago
Offer description

Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Athlone. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. E&I Lead required to lead and deliver Electrical and Instrumentation installation activities onsite for a major retrofit of an OSD pharmaceutical facility. The role is client-side, reporting to the E&I Work Package Owner/Senior Project Manager, and will be accountable for schedule, quality, safety, and compliance in a GMP environment. Candidates must have experience in pharma construction, proven management of EPCM partners and contractors as well as strong Quality/Technical attributes Duties: Serve as E&I Client Representative on site for all E&I activities throughout the delivery and execution phase, reporting to the E&I Work Package Owner/Senior Project Manager. The E&I lead will act as the client technical authority across installation activities ensuring delivery of Electrical & Instrumentation scopes. Manage interfaces between design team, construction, CQV (Commissioning, Qualification & Validation) and operations to ensure critical schedules are met, design is constructable and ensure smooth transition from Mechanical Completion (MC) to Commissioning & Qualification (C&Q). Oversee installation quality, manage vendor/contractor interfaces and drive resolution of technical issues across a complex programme. Monitor installation progress, quality and compliance with design and specifications, ensuring adherence to engineering, safety and quality standards. E&I Client rep in constructability reviews and sequencing plans. Provide clear structured reporting on progress, risks and issues. Drive risk management: identify, evaluate and mitigate risks; maintain and report risk registers. Manage turnover activities and ensure successful system handover to CQV and Operations including documentation, training and punch list closure. Ensure robust health, safety and environmental standards on site are being maintained by CM partner. Provide regular progress reporting (schedule, quality, HSE) and stakeholder communications to the E&I Work Package Owner/Senior Project Manager. Ensure best-practice quality management and documentation for GMP and GEP compliance(CTOP, VTOP, test packs, deviation reports). Drive resource planning and site resourcing to meet programme and milestones. Education and Experience: Degree qualification in Electrical Engineering. Relevant experience in pharmaceutical and GMP regulated manufacturing environments. Minimum 15 years project management experience, in a with demonstrable experience in pharmaceutical projects. Proven track record of managing E&I activities on large projects involving demolition, cleanrooms, HVAC, MEP, utilities and process equipment installation. Client-side experience or acting as client representative is a major benefit Strong experience managing EPCM partners, subcontractor performance Strong Quality/Turnover experience managing handover from W3 walkdowns through to successful system handover to Operations Demonstrated ability to manage interfaces with design teams and CQV/validation teams. Experience planning and delivering complex programmes with multiple work packages and discipline leads. Strong risk management and constructability review experience. Excellent stakeholder management and reporting skills; able to present to senior leadership and governance forums. Professional certifications (PMP, Prince2, NEBOSH, or equivalent) desirable. If interested in this posting please feel free to contact Avishek for further information.
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