3 дня назад
Supervisor, Manufacturing (Biotechnology)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Supervisor, Manufacturing (Biotechnology): Leading production personnel on high-throughput biotechnology manufacturing lines with an accent on production scheduling, quality compliance, workforce development, and process improvement. Focus on coordinating reagent, array, flowcell, or manifold production, troubleshooting operational issues, and transitioning processes into an efficient manufacturing setting.
Location: Singapore, Woodlands, NorthTech; onsite manufacturing environment
No salary specified.
Company
develops genomic technologies that support disease detection, diagnosis, treatment options, and advances in human health.
What you will do
- Lead and supervise production personnel on high-throughput biotechnology manufacturing lines.
- Oversee reagent, array, flowcell, or manifold production and ensure production goals are met.
- Schedule resources, manage work orders, review batch records and timesheets, track results, and coordinate shift handovers.
- Troubleshoot operational issues and implement process improvements in collaboration with Quality, Engineering, Shipping, and Planning.
- Write and revise work instructions and train technicians on documented processes.
- Recruit, onboard, develop, and manage the performance of employees within the department.
Requirements
- Diploma or equivalent studies required; a bachelor's degree or equivalent is preferred.
- 0–3 years of manufacturing experience, preferably including 1–2 years of supervisory experience.
- Experience with cGMP, ISO 13485, and ISO 9001 operations is required.
- Experience with inventory control and SAP or a similar system.
- Excellent communication, leadership, and interpersonal skills.
- This role is not eligible for visa sponsorship.
Nice to have
- Night-shift or 24/7 management experience.
- Hazardous chemicals experience.
- Pharmaceutical or life science product manufacturing experience.
- Knowledge of GMP regulations for clinical diagnostic products and experience transitioning processes from R&D to manufacturing.
Culture & Benefits
- Inclusive environment focused on belonging, collaboration, and diverse perspectives.
- Employee Resource Groups provide career development, cultural awareness, and social responsibility opportunities.
- Equal employment opportunity and pay equity commitments.
- Background checks may be conducted after a conditional offer.
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