6 дней назад
Supervisor, Manufacturing
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Supervisor, Manufacturing (Biotechnology Production): Leading high-throughput biotechnology production across reagent, array, flowcell, or manifold manufacturing with an accent on production targets, resource planning, quality compliance, and team development. Focus on managing rotating shifts, troubleshooting manufacturing issues, improving processes, and coordinating production with Quality, Engineering, Shipping, and Planning.
Location: Singapore - Woodlands - NorthTech. Onsite role requiring 12-hour rotating shifts with four monthly rotations between day and night.
Company
develops genomic technology that supports early disease detection, diagnosis, and new treatment options.
What you will do
- Lead production in reagent manufacturing, array, flowcell, or manifolds production.
- Ensure production goals, KPIs, schedules, and priorities are met.
- Schedule resources, track results, troubleshoot issues, review batch records, and manage work orders.
- Coordinate with Quality, Engineering, Shipping, and Planning groups.
- Write and revise work instructions and train technicians in their use.
- Recruit, onboard, develop, and manage the performance of production employees.
Requirements
- Diploma or equivalent required; a bachelor's degree is preferred.
- 0–3 years of manufacturing experience, preferably including 1–2 years of supervisory experience. Candidates with NTC/NITEC or high school qualifications and 10–15 years of relevant experience may also be considered.
- Experience with cGMP, ISO 13485, and ISO 9001 operations is required.
- Experience with inventory control and SAP or similar systems.
- Ability to work in noisy and chemical environments with appropriate PPE and distinguish component and chemical colors visually.
- Ability to work 12-hour rotating shifts, including day and night rotations.
Nice to have
- Night-shift or 24/7 management experience.
- Experience with hazardous chemicals.
- 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, openness, collaboration, and alternative perspectives.
- Employee Resource Groups provide career development, cultural awareness, and social responsibility opportunities.
- Equal opportunity employment and pay equity regardless of gender, ethnicity, or race.
- Background checks may be conducted after a conditional offer.
- This role is not eligible for visa sponsorship.
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