{"id":4283250,"url":"https://alion.io/job/rd-partners-equipment-project-engineer","title":"Equipment Project Engineer","company":{"id":4541649,"name":"R&D Partners","domain":"r-dpartners.com","url":"https://alion.io/company/r-and-d-partners","size_band":"11-50","is_staffing_agency":false,"employer_type":"staffing","is_intermediary":false,"listed_via":null,"ats_vendor":"Schema","truth_index":null},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":null,"employment_type":"contractor","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":[],"countries":[],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":30,"max":40,"currency":"EUR","period":"hour","gross":null,"usd_annual":88000},"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-11-09T00:00:00Z","employer_posted_date":"2026-11-09","last_verified_at":"2026-11-13T21:00:19Z","board_verified":true,"closed_at":null,"days_open":4,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":4},"description":"Are you an experienced Project Engineer ready to lead complex equipment and facility upgrades that support the future of biotechnology manufacturing?\nR&D Partners is seeking an experienced Equipment Project Engineer to join a leading biotechnology company in ROI. This fully onsite contract role offers an exciting opportunity to contribute to high-impact projects within a regulated GMP environment.\nPlease note that to be considered for this role you must have the right to work in this location.\n\nResponsibilities:\nManage all aspects of assigned projects, including schedule, cost, scope, safety, quality, and regulatory compliance.\nLead design management and ensure adherence to user requirements and GMP/GDP standards.\nCoordinate project meetings, document outcomes, and ensure timely action closure.\nOversee contractor and OEM performance to meet quality, schedule, safety, and GMP expectations.\nCollaborate with Document Control for timely submission of project documentation.\nPerform procurement activities, equipment acceptance, and infrastructure delivery while providing regular project status updates.\nEnsure compliance with environmental health and safety codes, KPIs, and performance standards.\nLiaise with internal and external stakeholders, suppliers, and vendors for seamless project execution.\nMentor project team members and maintain accurate project planning documentation.\nProvide weekly progress reports to management and senior stakeholders.\nReview engineering deliverables, initiate change controls, and manage project lifecycle documentation.\nDeliver performance metrics for budget, schedule, scope, and quality adherence.\nKey Skills and Requirements:\nProject Management: \nExpertise in project planning, scheduling, budgeting, and risk management.\nAbility to manage complex, multi-stakeholder projects within a regulated environment.\nTechnical Skills:\nExperience with production equipment qualification and GMP facility upgrades.\nStrong understanding of aseptic processing, contamination control strategies, and cleanroom design principles.\nFamiliarity with cleanroom classification standards (ISO 14644, EU GMP Grades A-D).\nKnowledge of qualification and validation lifecycle, including CSV, equipment qualification, and cleaning validation.\nUnderstanding of HVAC systems, pressure cascades, and environmental monitoring requirements.\nProficiency in MS Office and project management software.\nLeadership & Communication: \nProven ability to lead cross-functional teams and coordinate contractors in a GMP setting.\nStrong analytical, problem-solving, and decision-making skills.\nSafety & Compliance: \nEnsure all works are planned and executed safely under Safe Systems of Work.\nSupport Construction and Area Management teams for safe execution in GMP-controlled environments.\nEnsure full compliance with GMP, GDP, and Change Control processes.\nSupport regulatory inspection readiness and audit preparation activities (FDA, EMA).\nValidation & Qualification Coordination: \nCollaborate with CQV teams for equipment and facility qualification activities.\nAttend FATs and draft/review protocols and reports.\nSalary:\n€30.00 - €40.00/Hour\nFor more information, please contact Grant Van Schalkwyk.\nIf you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.\nR&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. 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