data analysisengineeringproject managementgmpprocess improvementlean manufacturingroot cause analysisdeviation managementvaccine manufacturingdeviation investigations
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
развернуть
$87к-137к/год
$85к$93кмедиана$100к
По похожим ролям (49) ~ $93к/год
84
Хорошая вакансия
развернуть
Чётко очерченная инженерная роль у крупного производителя вакцин даёт практический опыт GMP и работы над улучшением процессов; компромисс - возможны отдельные смены или выходные.
Иногда вне графика
Понятная зона задач
Производство вакцин
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Specialist, Engineering (Vaccine Manufacturing): Supporting live virus vaccine production and investigating manufacturing deviations across bulk vaccine production and final formulation and filling operations with an accent on GMP operations, equipment troubleshooting, process improvement, and technical documentation. Focus on identifying root causes, conducting full-scale experiments, implementing corrective actions, and supporting manufacturing operations in a hybrid West Point role.
Location: West Point, Pennsylvania, United States; hybrid work arrangement
Salary: $87,300–$137,400 per year, plus potential annual bonus and long-term incentive.
Company
hirify.global develops and manufactures pharmaceutical and vaccine products.
What you will do
Support production of live virus vaccines in bulk vaccine production and final formulation and filling operations.
Lead or contribute to manufacturing deviation investigations and process improvement projects.
Provide technical support on the manufacturing shop floor, including equipment troubleshooting and implementation of process or equipment actions.
Examine safety, compliance, automation, equipment, process, and personnel factors to identify and resolve root causes.
Design and conduct experimental protocols using technical operations laboratories or full-scale production equipment.
Author and update investigation, process design, engineering study, change control, and validation documentation.
Requirements
Bachelor’s degree in Engineering or Sciences.
At least one year of post-bachelor’s experience in GMP manufacturing or technical support for GMP manufacturing operations.
Ability to drive results and accountability, with strong communication and collaboration skills.
Strong problem-solving skills.
Ability to apply standardized work, engineering tools, and process tools consistently.
Nice to have
Vaccine manufacturing experience.
Sterile processing experience.
Experience authoring investigations.
Culture & Benefits
Hybrid work arrangement with primarily daytime, first-shift hours.
Limited off-shift or weekend coverage may be required based on business needs and assignments.
Medical, dental, vision, insurance, retirement benefits including 401(k), paid holidays, vacation, compassionate leave, and sick days.
No travel is required; no relocation support is provided.
Visa sponsorship is not available.
Inclusive workplace focused on collaboration, diverse perspectives, and respectful challenge.
Hiring process
Applications are accepted until the day before the stated posting end date, November 13, 2026.
US and Puerto Rico residents may request accommodation during the application or hiring process.
Будьте осторожны
Если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого. Это мошенники. Обязательно жмите «Пожаловаться» или пишите в поддержку. Подробнее в гайде →