process optimizationhseroot cause analysisindustry 4.0process validationcapacgmpequipment reliabilityapi manufacturing
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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В Company hidden предлагают чётко описанную позицию среднего уровня с серьёзными задачами в производстве лекарств, но без указанной зарплаты сложнее оценить привлекательность всего предложения.
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Зарплата не указанаПонятные задачиКрупный фармработодательШирокий круг задач
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Текст:
Hirify AI/Оригинал
TL;DR
Production Engineer (API Manufacturing): Supporting and optimizing API manufacturing operations at Sanofi's Jurong Plant with an accent on process reliability, equipment performance, quality compliance, and continuous improvement. Focus on troubleshooting production disruptions, leading deviation investigations and CAPA, supporting process validation and technology transfer, and implementing digitalization and Industry 4.0 initiatives.
Location: City of Singapore, Jurong Plant; onsite
Company
hirify.global develops medications and advances pharmaceutical science, with a focus on improving health outcomes.
What you will do
Provide technical and operational support for API manufacturing, monitoring production processes, equipment performance, output, quality, and compliance.
Troubleshoot production issues, equipment abnormalities, and process disruptions while coordinating with Manufacturing, Quality, Engineering, Supply Chain, HSE, and Continuous Improvement teams.
Develop and implement process optimization, Lean Manufacturing, hirify.global Manufacturing System, digitalization, automation, and Industry 4.0 initiatives.
Lead or support deviation investigations, root cause analysis, CAPA, change controls, risk assessments, audits, and regulatory inspection readiness.
Support process validation, qualification, technology transfer, equipment qualification, preventive maintenance coordination, and reliability improvement.
Maintain production procedures, batch records, manufacturing documentation, and quality records while promoting safe and compliant operations.
Requirements
Bachelor's degree in Chemical Engineering, Mechanical Engineering, Pharmaceutical Sciences, or a related discipline is required.
Minimum 3–5 years of relevant experience in pharmaceutical manufacturing, preferably in an API manufacturing environment.
Practical experience supporting production operations, manufacturing process optimization, and technical troubleshooting.
Experience driving continuous improvement and operational efficiency initiatives in a regulated manufacturing environment.
Strong understanding of API manufacturing operations, production processes, and equipment.
Working knowledge of cGMP, FDA, and applicable international pharmaceutical regulatory requirements.
Experience with equipment performance monitoring, deviation investigations, root cause analysis, CAPA, and change control.
Working knowledge of process validation, qualification, technology transfer, preventive maintenance coordination, and equipment reliability improvement.
Familiarity with Lean Manufacturing, SMS methodologies, digitalization, automation, Industry 4.0, HSE requirements, manufacturing risk assessments, and safe operating practices; strong analytical, problem-solving, and technical troubleshooting capabilities.
Nice to have
Experience supporting manufacturing investigations, validation activities, or technology transfers.
Experience in an API manufacturing environment.
Culture & Benefits
Full-time role based at the Jurong Plant in Singapore.
Work across Production, Manufacturing, Quality, Engineering, Supply Chain, HSE, and Continuous Improvement functions.
Environment focused on safety, quality, compliance, operational excellence, and continuous improvement.
Equal-opportunity workplace committed to inclusion and diversity.
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