{"id":3011008,"url":"https://alion.io/job/h-b-fuller-quality-validation-specialist","title":"Quality & Validation Specialist","company":{"id":97848,"name":"H.B. Fuller","domain":"hbfuller.com","url":"https://alion.io/company/hbfuller-2","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":81,"open_postings":12,"ghost_share":0,"stale_share":0.75,"repost_share":0,"time_to_fill_p50_days":31,"computed_at":"2026-10-24T06:02:35Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":"junior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Dublin, Ireland"],"countries":["IE"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":38000,"max_usd":77000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":10},"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"FMEA","optional":false},{"name":"GMP","optional":false},{"name":"HPLC","optional":false},{"name":"ISO 13485","optional":false}],"status":"live","first_seen_at":"2026-10-21T15:23:16Z","employer_posted_date":"2026-10-21","last_verified_at":"2026-10-24T17:41:42Z","board_verified":true,"closed_at":null,"days_open":3,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":3},"description":"As the largest pureplay adhesives company in the world, H.B. Fuller’s (NYSE: FUL) innovative, functional coatings, adhesives and sealants enhance the quality, safety and performance of products people use every day. Founded in 1887, with 2025 revenue of $3.5 billion, our mission to Connect What Matters is brought to life by more than 7,100 global team members who collaborate with customers across more than 30 market segments in 150 countries to develop highly specified solutions that enable customers to bring world-changing innovations to their end markets. Learn more at www.hbfuller.com.\nPosition Overview\nThe Quality & Validation Chemist Specialist supports validation, quality, and laboratory activities within a regulated medical device or pharmaceutical manufacturing environment. This role ensures processes, equipment, analytical methods, and quality systems remain compliant with GMP, ISO, and regulatory requirements while providing technical expertise in chemistry and analytical testing.\nPrimary Responsibilities\nExecute and document process, cleaning, analytical method, and equipment validation activities.\n\nSupport equipment and system qualification (IQ/OQ/PQ).\n\nPrepare and review validation protocols, reports, risk assessments, and supporting documentation.\n\nInvestigate deviations, non-conformances, and out-of-specification (OOS) results.\n\nPerform root cause analysis and support CAPA development and effectiveness reviews.\n\nReview batch records, validation data, and quality documentation for compliance.\n\nInterpret analytical data from techniques such as HPLC, GC, UV, and FTIR.\n\nSupport internal, supplier, and regulatory audits and inspections.\n\nMaintain compliance with GMP, ISO, FDA, EMA, and data integrity requirements.\n\nCollaborate with Quality, Laboratory, and Operations teams to drive continuous improvement.\n\nMinimum Requirements\nBachelor's degree in Chemistry or a related scientific discipline.\n\n2-5 years of experience in a pharmaceutical, medical device, or regulated manufacturing environment.\n\nHands-on experience with validation activities, including process, cleaning, analytical, or equipment validation.\n\nKnowledge of GMP, ISO 13485, FDA, or EU regulatory requirements.\n\nStrong technical writing, documentation, and problem-solving skills.\n\nPreferred Requirements\nPostgraduate qualification or certification in Quality, Validation, or a related field.\n\nExperience supporting FDA, or Notified Body inspections.\n\nKnowledge of quality risk management tools, including FMEA, Fishbone, or 5 Whys.\n\nExperience with electronic Quality Management Systems (eQMS).\n\nFamiliarity with automation testing, scripting, or GAMP5 frameworks.\n\nH.B. Fuller is an Equal Employment Opportunity employer and proud to have created a collaborative culture where employees around the world are seen, heard, and respected. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, or marital status or status as a protected veteran, or any other legally protected classification.\nH.B. Fuller does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with H.B. Fuller, a written service agreement must be executed by Human Resources prior to submitting any information relating to a potential candidate. Without a signed service agreement, H.B. 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