4 дня назад
Manufacturing Supervisor (Biotechnology)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Manufacturing Supervisor (Biotechnology): Leading cleanroom manufacturing operations in Incheon with an accent on production scheduling, operator coordination, deviation response, and GMP-compliant documentation. Focus on balancing demand, capacity, materials, quality, and delivery while applying Lean, Six Sigma, root cause analysis, and Kaizen to improve production flow.
Location: On-site in Song-Do, Incheon, Korea; remote work arrangement may be available for eligible roles
Company
Cytiva is a operating company providing life sciences, diagnostics, and biotechnology solutions that support biological research, vaccines, medicines, and cell and gene therapies.
What you will do
- Lead daily cleanroom production operations and execute strategies based on customer demand, capacity, material availability, and business priorities.
- Build and revise production schedules with Material Planning and S&OP teams, while coordinating operator staffing, shifts, workload allocation, coaching, and handovers.
- Maintain accurate batch records, deviation reports, and production documentation, ensuring audit readiness and compliance with GMP, quality, cleanroom, biohazard, and EHS requirements.
- Coordinate equipment qualification, preventive maintenance, troubleshooting, and process readiness with Quality and Engineering.
- Monitor QDIP metrics through ERP systems and data analytics, applying Lean, standard work, visual management, root cause analysis, and Kaizen to improve productivity and reduce waste.
Requirements
- Bachelor’s degree in Industrial or Chemical Engineering, Biotechnology, Logistics, or a related field.
- At least 10 years of manufacturing operations experience, including production team leadership and daily operations management.
- Experience balancing production schedules, demand, resources, quality, delivery, equipment readiness, process control, and safety requirements.
- Strong decision-making, prioritization, communication, and cross-functional leadership skills, including hands-on leadership during critical shop-floor situations.
- Proficiency with ERP systems such as SAP or Oracle, plus data analysis, forecasting, reporting, and continuous improvement methods including Lean, Six Sigma, or Kaizen.
- Fluent written and verbal English and Korean; foreign nationals must have a legal work permit under Korean immigration law. A valid driver’s license, acceptable driving record, ability to travel abroad, and ability to lift or carry equipment up to 30 lb are also required.
Nice to have
- CPIM, CSCP, or a related professional certification.
- Experience with EHS compliance, biosafety, containment, cleaning validation, or contamination control in biologics or cleanroom environments.
- Experience with tech transfer, commissioning, and IQ/OQ/PQ equipment or facility qualification and validation.
- Leadership experience in continuous improvement, cost optimization, waste reduction, or yield improvement projects in biologics or biopharmaceutical manufacturing.
Culture & Benefits
- Comprehensive benefits including healthcare programs and paid time off.
- Continuous improvement culture supported by the Business System.
- Flexible and remote working arrangements may be available for eligible roles.
- Work focused on life sciences, biotechnology, and solutions that support human health.
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