Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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В Company hidden четко описана роль в производстве биопрепаратов с ответственностью за оборудование и участием во внедрении новых продуктов, но без указанной зарплаты сложно оценить условия оплаты.
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Зарплата не указанаЧеткая зона ответственностиСильная биотех-сфераПоддержка развитияРабота вне графика
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Engineer I – Process Engineering (Biologics Process Equipment) (Biologics Manufacturing): Supporting and owning process equipment for upstream and downstream biologics manufacturing, including equipment performance, maintenance, validation, and new product introduction with an accent on cGMP compliance, equipment readiness, and cross-functional operations. Focus on investigating equipment deviations, implementing corrective actions, maintaining validated systems, and improving reliability through data analysis and lifecycle planning.
Location: Singapore Manufacturing - Tuas; on-site
Company
hirify.global develops medicines and applies biology and technology to serve patients with serious illnesses.
What you will do
Own day-to-day engineering support, performance, maintenance planning, lifecycle actions, and validated state for an assigned portfolio of biologics process equipment.
Provide subject matter expertise for upstream and downstream equipment used in cell culture, harvest filtration, viral inactivation, purification, and drug substance bulk fill.
Lead equipment investigations, identify root causes, recommend corrective and preventive actions, and drive approved actions to closure.
Support change controls, deviations, qualifications, inspections, and equipment-readiness deliverables for new product introduction and site projects.
Improve equipment reliability, maintenance optimization, safety, efficiency, and operational sustainability using performance data and advanced technologies.
Collaborate with Manufacturing, Maintenance, Quality, Engineering, project teams, and corporate engineering on equipment design, modifications, and technical solutions.
Requirements
Master’s degree in Engineering, or a Bachelor’s degree with 2 years of directly related experience.
Alternatively, an Associate’s degree with 4 years of directly related experience, or a high school diploma/GED with 6 years of directly related experience.
Experience managing stakeholders and process equipment in a biopharmaceutical environment is preferred.
Knowledge of biopharmaceutical processes, equipment validation, qualification documentation, and critical utilities is preferred.
Knowledge of automation systems such as DeltaV, BMS, ladder logic, and PLC is preferred.
Ability to work independently, collaborate across functions, solve technical problems, and work off-hours when required.
Nice to have
Experience with FAT, SAT, IQ, OQ, PQ, commissioning, qualification, and system handover.
Project management experience covering schedules, costs, facilitation, and follow-up.
Knowledge of Total Productive Maintenance and Reliability Centered Maintenance.
Culture & Benefits
Collaborative environment focused on continuous learning and meaningful work.
Professional development opportunities and support for personal growth.
Medical checks required for the role are arranged with related expenses covered by the company.
Inclusive workplace committed to diversity, ethics, respect, and equal opportunity.
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