{"id":3163318,"url":"https://alion.io/job/hikma-pharmaceuticals-senior-production-engineer","title":"Senior Production Engineer","company":{"id":1843927,"name":"Hikma Pharmaceuticals","domain":"hikma.com","url":"https://alion.io/company/hikma","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Phenom","truth_index":null},"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":["Columbus, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":75000,"max_usd":142000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":6333},"experience_years_min":12,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"AutoCAD","optional":false},{"name":"Microsoft Office","optional":false},{"name":"Microsoft Project","optional":false}],"status":"live","first_seen_at":"2026-09-18T00:00:00Z","employer_posted_date":"2026-10-23","last_verified_at":"2026-10-29T17:59:06Z","board_verified":true,"closed_at":null,"days_open":41,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":41},"description":"Job Title: Engineer III, Production\nLocation: Columbus, OH\nJob Type: Full-Time\nReq ID: 12359\nDescription:\nWe are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Engineer III, Production to join our team.\nIn this role, you will be responsible for providing engineering solutions to analyze equipment/process capacity constraints and long-term strategic vision for all equipment operation and capacities. Use this information to make recommendations for existing equipment/process modifications or new equipment purchases that coincide with this strategic plan. Investigate new equipment options, make recommendations and implement. Capital management focus.\nKey Responsibilities:\nRegular and predictable onsite attendance and punctuality.\nProvide technical support to the assigned production area on existing equipment in terms of operating efficiently, troubleshooting problems, coordinating technical activities with maintenance, and analyzing and communicating technical issues to production and engineering staff.\nAnalyze equipment capabilities and specify, set-up equipment for new product launch.\nMonitor the process and calculate data for production equipment to implement continuous improvement activities.\nEvaluate equipment to increase capacity and upgrade technology.\nMentor Production Engineers I and II.\n\nQualifications:\nWe value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them.\nBS in Pharmaceutics, Engineering, or a related scientific discipline with 5+ years of experience, or 12+ years of equivalent experience, supporting pharmaceutical production equipment.\nDemonstrated ability to work independently with minimal supervision, applying engineering principles and technical expertise.\nStrong planning and technical support skills for large capital projects.\nExperience leading 1-2 capital and expense projects ranging from $0-$2 million, including schedule, cost, and deliverable management.\nProven ability to identify complex problems, evaluate options, and implement effective solutions.\nStrong analytical, logical reasoning, and decision-making skills.\nExcellent listening, interpersonal, and communication skills.\nEffective time management skills, including the ability to prioritize personal and team activities.\nStrong written communication skills, including preparation of technical documentation for FDA, OSHA, and other regulatory agencies.\nAbility to effectively communicate technical information related to manufacturing processes, material flow, quality control, and operational efficiency.\nStrong presentation skills with the ability to train and educate technicians on equipment principles and operation.\nAt least one year of validation experience qualifying equipment using GAMP methodology to meet production and process specifications.\nProficient with AutoCAD, Microsoft Office Suite, Microsoft Project, SAP, and equipment-specific software.\nHands-on experience with pharmaceutical manufacturing equipment, including fluid beds, CIP systems, one-pot granulators, tablet presses, encapsulators, pumps, comils, processors, dryers, coating pans, bin tumblers, and micronizers.\nWorking knowledge of 21 CFR regulations related to pharmaceutical production equipment.\nDemonstrated conflict management and resolution skills.\nAbility to influence and develop project team members without direct authority.\nEqual Opportunity Employer:\nHikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. 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