{"id":1455362,"url":"https://alion.io/job/sigmar-recruitment-validation-engineer","title":"Validation Engineer","company":{"id":1898812,"name":"Sigmar Recruitment","domain":"sigmarrecruitment.com","url":"https://alion.io/company/sigmarrecruitment","size_band":"51-200","is_staffing_agency":true,"employer_type":"agency","is_intermediary":false,"listed_via":null,"ats_vendor":"Schema","truth_index":{"grade":"A","score":100,"open_postings":8,"ghost_share":0,"stale_share":0,"repost_share":0,"time_to_fill_p50_days":24,"computed_at":"2026-10-12T06:55:09Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":null,"employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Roscommon, Ireland"],"countries":["IE"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":48000,"max":48000,"currency":"EUR","period":"year","gross":null,"usd_annual":54611},"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-09-21T00:00:00Z","employer_posted_date":"2026-09-21","last_verified_at":"2026-10-12T14:51:53Z","board_verified":true,"closed_at":null,"days_open":21,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":21},"description":"Validation Engineer | Roscommon | 2-Year FTC\nAbout Your New Employer\nAn established pharmaceutical manufacturing company in Co. Roscommon is looking to recruit a Validation Engineer on a 2-year fixed-term contract.\nThis is a hands-on role within a regulated GMP pharmaceutical environment, with responsibility across a broad range of site validation activities.\nAbout Your New Job\nAs a Validation Engineer, you will:\nSupport and manage equipment qualification (IQ/OQ/PQ) activities, including protocols and reports.\nCoordinate process and cleaning validation activities.\nSupport Computer System Validation (CSV) activities.\nMaintain validation documentation, including the Validation Master Plan, protocols, reports and SOPs.\nSupport the site's calibration programme and associated documentation.\nInvestigate validation-related deviations and support CAPA and change control.\nSupport qualification of new equipment and periodic equipment reviews.\nProvide validation support during regulatory and customer audits.\nWork with Quality, Engineering and Production to deliver validation activities to agreed timelines.\nWhat You Need\nPrevious Validation Engineer experience within a pharmaceutical GMP environment.\nStrong knowledge of equipment, process and cleaning validation, including IQ/OQ/PQ.\nGood understanding of GMP, validation documentation and calibration.\nStrong technical writing, organisational and communication skills.\nWhat’s Next?\nFor more information on this 2-year FTC Validation Engineer opportunity in Co. 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