Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$96к-126к/год
$120к$140кмедиана$170к
По похожим ролям (48) ~ $140к/год
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Роль четко описана и дает возможность отвечать за инженерные системы коммерческого производства клеточной терапии, а пакет льгот выглядит содержательным; при этом важно учитывать работу на площадке и быстрый темп в среде GMP.
?Работа на площадке
Клеточная терапия
Понятная зона ответственности
Хорошие льготы
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Engineer (Biotech): Providing technical leadership for GMP facilities, utilities, and commercial cell therapy manufacturing equipment with an accent on equipment lifecycle management, compliance, and operational excellence. Focus on troubleshooting, root cause investigations, validation, maintenance strategy optimization, and leading cross-functional capital and improvement projects.
Location: Onsite in Raritan, New Jersey, United States. Applicants must be authorized to work in the United States and employment eligibility will be verified through E-Verify.
Base salary: $96,267–$126,351 USD per year, with performance-based bonus and/or equity available for eligible roles.
Company
hirify.global is a global biotechnology company developing cell therapies, including CAR-T, TCR-T, and NK cell-based therapies, with a collaboration with Johnson & Johnson on CARVYKTI.
What you will do
Own the lifecycle of GMP facilities, utilities, and cell therapy manufacturing process equipment.
Lead troubleshooting, root cause investigations, deviation support, CAPAs, and change controls.
Deliver COGM reduction and Operational Excellence initiatives while monitoring system performance.
Develop preventive and predictive maintenance strategies.
Support commissioning, qualification, validation, startup, and turnover activities.
Author and review SOPs, technical reports, and specifications; lead cross-functional projects and manage contractors and vendors.
Requirements
Bachelor’s degree in Mechanical, Electrical, Chemical, or Industrial Engineering, or a related discipline; a master’s degree is preferred.
At least 7 years of engineering, facilities, maintenance, or operations experience in a GMP-regulated environment.
Experience leading equipment and utility projects from concept through implementation.
Knowledge of commissioning, qualification, validation, change control, and deviation management processes.
Strong project management and communication skills, with the ability to manage multiple priorities in a fast-paced environment.
Experience mentoring engineers and leading cross-functional initiatives.
Ability to ensure compliance with cGMP, EHS, and regulatory requirements and support audits and inspections.
Nice to have
Experience supporting biotechnology, pharmaceutical, or cell therapy manufacturing.
Proven Lean/TPS implementation and Operational Excellence leadership experience.
Master’s degree in an engineering discipline.
Culture & Benefits
Permanent full-time employment with medical, dental, vision, and 401(k) benefits; contractors are not eligible for these benefits.
Eight weeks of paid parental leave after three months of employment and paid time off including vacation, personal, sick time, floating holidays, and company holidays.
Additional benefits include flexible spending and health savings accounts, insurance programs, commuter benefits, family-care resources, well-being initiatives, and recognition programs.
Employment is at-will and subject to applicable federal, state, and local requirements.
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