Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Роль четко описана и связана с запуском крупного производства мРНК-препаратов, но стоит учитывать периодическую работу вне обычных часов и обязательное присутствие на площадке.
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Дежурства вне графикаШирокая зона задачАктуальные технологииРазвитие производстваБиотехнологии
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Automation Engineer – Packaging & Process Automation (Pharmaceutical Manufacturing): Supporting and commissioning automated packaging and drug substance manufacturing systems at a UK mRNA manufacturing facility with an accent on PLCs, Emerson DeltaV, packaging equipment, validation, and compliant operations. Focus on troubleshooting multidisciplinary automation issues, delivering systems through commissioning and qualification, improving equipment reliability and performance, and maintaining GxP-controlled environments.
Location: Oxford, England, United Kingdom; 100% onsite.
Company
hirify.global develops mRNA medicines and is establishing a research, development, and manufacturing facility at Harwell for onshore mRNA vaccine production in the UK.
What you will do
Provide hands-on automation engineering support for drug product packaging and drug substance manufacturing operations.
Troubleshoot and optimise PLCs, Emerson DeltaV systems, HMIs, instrumentation, industrial networks, machine controls, servo and motion systems, vision technologies, and equipment interfaces.
Support automated labelling, secondary packaging, serialization, aggregation, inspection, printing, conveying, robotics, and material-handling systems.
Deliver automation projects through design, FAT, SAT, commissioning, qualification, validation, start-up, and handover to manufacturing.
Investigate failures, downtime, quality events, and deviations; implement root-cause corrective and preventive actions.
Maintain compliant automation documentation and validated systems while improving reliability, OEE, changeovers, integration, lifecycle management, and manufacturing performance.
Requirements
Bachelor of Science degree in Mechanical Engineering, Electrical Engineering, Automation Engineering, Manufacturing Engineering, Packaging Engineering, or a related technical discipline.
3+ years of automation engineering experience supporting manufacturing equipment, preferably in pharmaceutical, biotechnology, medical device, or another highly regulated industry.
Experience troubleshooting and supporting automated manufacturing or packaging equipment in a GMP/GxP-regulated manufacturing environment.
Ability to troubleshoot complex multidisciplinary equipment problems involving mechanical, electrical, controls, and automation systems.
Experience supporting equipment changes through formal engineering and quality-system processes.
Clear communication skills for explaining complex technical information to manufacturing personnel, technical teams, leadership, vendors, and Quality stakeholders.
Ability to work independently in a fast-paced manufacturing environment and drive technical issues to resolution.
Flexibility to provide occasional off-hours, holiday, and weekend support.
Nice to have
Knowledge of pharmaceutical drug product packaging operations and packaging-line equipment.
Experience with packaging OEMs and technologies including Marchesini, Optima, Syntegon/Bosch, Körber, Antares Vision, Cognex, Keyence, Zebra, Videojet, Domino, Rockwell Automation, or similar systems.
Proficiency with Allen-Bradley/Rockwell PLCs, HMIs, servo systems, industrial networks, and machine controls.
Experience with machine vision, automated inspection, serialization, aggregation, and Level 1–4 packaging architecture.
Familiarity with 21 CFR Part 11, electronic records and signatures, data integrity, and computerized system lifecycle principles.
Knowledge of packaging quality topics including label control, reconciliation, vision inspection, barcode grading, tamper evidence, container and closure integrity interfaces, and product traceability.
Experience with Lean Manufacturing, Six Sigma, FMEA, RCA, structured problem solving, reliability engineering, manufacturing data, historians, MES, CMMS, or analytics tools.
Ability to learn new equipment, technologies, and manufacturing processes quickly; interest in contributing to a high-growth, transformational company with Bold, Relentless, Curious, and Collaborative values.
Culture & Benefits
In-person, site-based work with close collaboration across Engineering, Manufacturing, Maintenance, Quality, Validation, Supply Chain, Automation, Digital, and external partners.
Competitive healthcare and voluntary benefits, with location-specific perks.
Fitness, mindfulness, mental health, and other well-being support.
Family-building benefits including fertility, adoption, and surrogacy support.
Paid vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown.
Savings and investment programs, plus a smoke-free, alcohol-free, and drug-free workplace.
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