{"id":2656749,"url":"https://alion.io/job/biogen-senior-fill-finish-process-engineer","title":"Senior Fill Finish Process Engineer","company":{"id":449685,"name":"Biogen","domain":"biogen.com","url":"https://alion.io/company/biogen-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":75,"open_postings":19,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":27,"computed_at":"2026-10-22T06:10:10Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Athlone, Ireland"],"countries":["IE"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":69000,"max_usd":120000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":57},"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-10-15T23:09:18Z","employer_posted_date":"2026-10-15","last_verified_at":"2026-10-22T06:12:39Z","board_verified":true,"closed_at":null,"days_open":7,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":7},"description":"About This Role\nThe Senior Fill Finish Process Engineer is a site-based member of the Global Engineering & Facilities within the Drug Product Engineering Technical Authority. The role provides technical leadership for aseptic fill-finish and sterile drug-product manufacturing systems, with accountability spanning facility-fit assessments, feasibility studies, front-end capital planning, engineering design, project execution and operational readiness.\nAs the primary GEF interface at the Athlone site, the position connects site stakeholders with Biogen’s Global Engineering Technical Authorities and coordinates the appropriate discipline support for capital projects, technical assessments and operational priorities. The engineer applies lifecycle-based engineering practices to ensure that facilities, equipment and systems are safe, compliant, reliable, scalable and aligned with Biogen standards and long-term manufacturing strategy.\nWhat You'll Do\nAseptic Manufacturing & Drug Product Engineering\nServe as a Subject Matter Expert (SME) for aseptic filling, sterile manufacturing processes, isolators, RABS, lyophilization, autoloading systems, and associated drug product technologies.\nProvide engineering leadership and technical guidance for drug product manufacturing systems throughout their lifecycle.\nSupport technical due diligence, process evaluations, and manufacturing network assessments.\nPartner with site engineering and operations teams to identify opportunities for process improvements, capacity expansion, and technology deployment.\nFacility Fit & Feasibility Studies\nLead Facility Fit Assessments for new products, technologies, and manufacturing opportunities.\nDevelop and execute feasibility studies for facility modifications, capacity expansion projects, and new manufacturing investments.\nEvaluate process, equipment, utility, infrastructure, automation, and facility requirements to support informed project decisions.\nSupport business case development and capital planning activities.\nCapital Projects & Engineering Design\nSupport the development and execution of capital projects from concept through operational readiness.\nCollaborate with Engineering & Architectural (A&E) firms during feasibility, conceptual design, FEED, detailed design, and construction activities.\nReview engineering deliverables including layouts, process flow diagrams, equipment specifications, utility assessments, and design packages.\nEnsure projects align with Biogen engineering standards, GMP requirements, and long-term technical strategies.\nProvide technical leadership during project reviews, design workshops, and stage-gate governance activities.\nSite Technical Authority Representation\nAct as the on-site representative for Global Engineering & Facilities.\nProvide local coordination and support for Drug Product, Facilities, Automation, and other Technical Authority functions as required.\nFacilitate communication and alignment between global technical authorities and site stakeholders.\nSupport engineering investigations, technical assessments, and site operational issues as required.\nNew Opportunities\nSupport assessments of other future modalities as required - finished goods, packaging, assembly, labeling, and related manufacturing opportunities.\nParticipate in strategic evaluations for future facility expansions and capability development.\nProvide engineering support for technology transfers and implementation of new manufacturing platforms.\nTechnology & Innovation\nMonitor industry trends, emerging technologies, and best practices in aseptic processing and pharmaceutical manufacturing.\nSupport development and deployment of engineering standards, specifications, and best practices.\nPartner with vendors, equipment suppliers, and industry experts to identify innovative technical solutions.\nDrive continuous improvement and engineering excellence across the manufacturing network.\nWho You Are\nYou are a highly capable engineering professional with strong experience in sterile pharmaceutical manufacturing, facility design, and capital project execution. You apply sound engineering judgement to complex and sometimes ambiguous problems, translate technical risks into practical recommendations, and influence decisions across site, global and external stakeholders\nYou are comfortable influencing stakeholders across all organizational levels and can effectively represent Global Engineering & Facilities within a manufacturing site environment.\nRequired Qualifications\nBachelor's degree in Mechanical, Chemical, Industrial, Pharmaceutical, or related Engineering discipline.\nEngineering experience within the pharmaceutical, biotechnology, medical device, or related regulated manufacturing industries.\nExperience supporting aseptic manufacturing operations and sterile processing technologies.\nExperience with facility fit assessments, engineering evaluations, and feasibility studies.\nExperience supporting capital projects and facility modifications.\nWorking knowledge of GMP requirements and pharmaceutical facility design principles.\nStrong communication, technical writing, and presentation skills.\nDemonstrated ability to influence cross-functional teams and senior stakeholders.\nPreferred Qualifications\nExperience within an Engineering & Architectural (A&E) consulting firm.\nExperience supporting fill-finish manufacturing facilities and sterile product operations.\nKnowledge of isolator technology, RABS, lyophilization, material transfer systems, Automated Visual Inspection systems and contamination control strategies.\nExperience with Front-End Engineering Design (FEED), conceptual design, and detailed design activities.\nExperience supporting packaging, finished goods, or secondary manufacturing operations.\nMaster's degree in Engineering or related discipline.\nProfessional Engineering (PE) registration or equivalent engineering certification.\nJob Level: ProfessionalWhy Biogen?\nWe are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.\nAt Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen.\nAll qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. 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