{"id":4050703,"url":"https://alion.io/job/inteldot-sr-engineer-35953","title":"Sr. Engineer 35953","company":{"id":4418608,"name":"Inteldot","domain":"inteldot.com","url":"https://alion.io/company/inteldot","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Breezy","truth_index":null},"role":"Backend","role_family":"Backend","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":["Juncos, Puerto Rico"],"countries":["PR"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false},{"name":"JMP","optional":false},{"name":"Power BI","optional":false},{"name":"SQL","optional":false},{"name":"CAPA","optional":true},{"name":"Chromatography","optional":true},{"name":"Power Automate","optional":true},{"name":"Smartsheet","optional":true}],"status":"live","first_seen_at":"2026-11-10T22:19:26Z","employer_posted_date":"2026-11-10","last_verified_at":"2026-11-11T01:32:46Z","board_verified":true,"closed_at":null,"days_open":0,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":0},"description":"Inteldot has over 15 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.\nAdministrative Shift (8:00 AM - 5:00 PM)\nJob Description:\nIndependently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. Applies advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, process and/or capital projects. Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity.\nRequirements & Qualifications:\nExperience supporting manufacturing process and operations in a GxP/GMP environment, with a solid understanding of process performance, equipment, and manufacturing workflows.\nExperience with manufacturing systems and processes such as DME, PLM, Change Control, MMP/MPP management, and Continuous Process Verification (CPV).\nExperience supporting controlled document and process changes, including document updates, coordination of reviews and approvals, implementation activities, and associated GMP documentation.\nExperience supporting Continuous Process Verification (CPV) activities, including process data review, evaluation of process performance and variability, identification of trends, preparation of periodic CPV reports and presentations, and escalation of potential process performance issues.\nAbility to interpret manufacturing and process data to support process monitoring, investigations, troubleshooting, and continuous improvement activities.\nStrong proficiency with Excel and experience with process data trending, analysis, and visualization tools such as JMP and/or Power BI.\nAbility to perform system configuration activities, including understanding business and process requirements, evaluating configuration needs, implementing, or supporting configuration changes, testing changes, documenting results, and troubleshooting system or process issues.\nExperience working with controlled documentation, data integrity requirements, and GMP systems, and change management processes.\nFamiliarity with SQL for data querying, troubleshooting, data verification, and investigation of system or process-related issues is preferred.\nFamiliarity with digital tools and automation solutions used to improve manufacturing workflows, reporting, process monitoring, or system activities is considered a plus.\nFamiliarity with tools such as Smartsheet and/or Microsoft 365 solutions, Power BI, Power Query, Power Automate, SQL, or similar technologies is considered a plus.\nKnowledge of manufacturing processes, including equipment, devices, packaging, and/or process operations, is preferred.\nExperience supporting APR, CPV, process monitoring, manufacturing performance reporting, and/or continuous improvement activities is considered a strong plus.\nStrong engineering, analytical and technical problem-solving skills, with the ability to evaluate manufacturing, process and system issues and identify practical solutions.\nExcellent written and verbal communication skills, with the ability to interact effectively across different communication and working styles.\nFully bilingual in English and Spanish.\nResponsibilities:\nSupport manufacturing/process engineering activities, system configuration, and support (including DME and PLM), CPV activities, controlled documentation, and manufacturing process monitoring.\nPerforming System Owner assessments and engineering impact assessments related to equipment failures, process deviations, and quality events.\nSupporting technical investigations, identifying equipment failure mechanisms, and developing corrective and preventive actions to reduce recurrence.\nEvaluating the applicability of CAPA and lessons learned to other equipment, systems, and manufacturing areas.\nManaging engineering activities in IBM Maximo, including work order technical review, pre-approval and post-approval activities, maintenance coordination, and follow-up through closure.\nDeveloping and revising preventive maintenance strategies, Job Plans, inspection requirements, and SOPs.\nImplementing engineering controls and completing actions associated with safety incidents and INCA records.\nSupporting equipment troubleshooting, repair coordination, replacement of obsolete equipment, spare parts evaluations, and equipment modernization projects.\nWorking with biopharmaceutical manufacturing equipment such as centrifuges, autoclaves, process tanks, chromatography and UF/DF systems, homogenizers, filter integrity testers, and associated instrumentation.\nPreparing clear technical reports and assessment rationales, maintaining traceable supporting documentation, and completing actions within established deadlines.\nCoordinating with Manufacturing, Process Engineering, Maintenance, Quality, Automation, Validation, and equipment suppliers.\nManaging multiple concurrent assignments and prioritizing work according to safety, quality, and operational needs.\nEducation:\nBachelor degree in Engineering, such as Chemical, Mechanical, Electrical, Industrial, Biomedical, or related engineering 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