Associate Manager, Development Services - Purification (Biotech)
Контакты
Формат работы
hybrid
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
Singapore
people managementcgmpchromatographyultrafiltrationprocess characterizationaktaviral clearancedownstream process developmentdiafiltration
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
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$105к$132кмедиана$173к
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В Company hidden чётко описана руководящая роль в разработке биопрепаратов, но без зарплаты сложно оценить условия по сравнению с рыночным ориентиром.
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Зарплата не указанаПонятная зона ответственностиКрупная биотех-компанияПрактичные льготыБиотехнологии
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Associate Manager, Development Services - Purification (Biotech): Leading a team delivering late-stage development, process characterization, and viral clearance activities in downstream purification with an accent on cGMP compliance, resource planning, and customer-focused project delivery. Focus on coaching scientists and analysts, reviewing technical documentation, presenting data to customers, and managing risks, audits, and cross-functional execution.
Location: Tuas, Singapore; office-first with remote work permitted for 20% of the time, or one day per week.
Company
hirify.global is a global life sciences company with more than 30 sites across five continents, manufacturing medicines and supporting customers in developing therapies.
What you will do
Lead a team of 9–10 scientists and analysts performing downstream purification, process development, process characterization, and viral clearance activities.
Drive late-stage development, process characterization, and viral clearance work while ensuring timely, high-quality project delivery.
Manage team, equipment, and system resources in line with department sales plans, including project, risk, escalation, and resource management.
Coach and develop team members and act as a subject matter expert in key technical areas.
Oversee documentation, review, and approval of reports and protocols, ensuring EHS, cGMP, audit, quality, and compliance requirements are met.
Present data to customers and support proposals, presentations, lab tours, business development, and cross-functional project delivery.
Requirements
Degree, PhD, or equivalent qualification in a relevant science field.
Relevant experience in downstream process development, process characterization, or viral clearance.
Laboratory-scale experience with affinity and ion exchange chromatography using the AKTA system, ultrafiltration/diafiltration, and viral reduction strategies.
2–5 years of experience leading a team in a people manager role.
Excellent problem-solving and analytical skills.
Good understanding of cGMP regulations.
Nice to have
Experience in process characterization and viral clearance studies.
Culture & Benefits
Agile career environment and dynamic working culture.
Inclusive and ethical workplace focused on collaboration, accountability, excellence, passion, integrity, and diversity.
Compensation programs recognizing high performance.
Daily company bus service from an MRT location near home to and from the Tuas site.
Fully paid medical insurance, with the option to enroll family members at partially subsidized premiums.
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