Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
развернуть
$90к-130к/год
$94к$120кмедиана$160к
По похожим ролям (47) ~ $120к/год
На СНГ рынке: $1.9к/мес ($1.4к - $3к)
84
Хорошая вакансия
развернуть
Чётко очерченная руководящая роль в крупной биофармацевтической компании даёт опыт запуска нового производства биопрепаратов, но работа проходит на площадке и связана с высокой операционной нагрузкой.
?Работа на производстве
Запуск нового объекта
Понятная зона ответственности
Развитие карьеры
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Supervisor Manufacturing (Biologics Manufacturing): Leading manufacturing operations in a new large-scale cGMP biologics facility through commissioning, process validation, product changeover, and ongoing support operations with an accent on staff leadership, production compliance, and quality systems. Focus on supervising manufacturing teams, operating complex equipment, resolving production-floor issues, and implementing continuous improvement projects.
Location: Framingham, Massachusetts, United States; position is for US and Puerto Rico residents only.
Salary: $90,000–$130,000 per year.
Company
hirify.global is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines to improve global health.
What you will do
Lead, coach, mentor, train, and develop manufacturing staff while maintaining supervisory continuity.
Supervise large or multiple small teams, assign work, develop plans, and maintain production schedules.
Support facility start-up from operational commissioning and shakedown through process validation and product changeover.
Operate complex systems and equipment, maintain documentation, and investigate and escalate issues involving processes, equipment, automation, utilities, materials, or systems.
Lead continuous improvement projects, establish and report performance metrics, conduct applicable internal audits, and ensure projects are completed on schedule.
Requirements
High school diploma/GED with 5–10 years of experience in a cGXP environment, or a bachelor’s degree with 4–8 years of experience.
At least 1 year of experience in a lead or supervisor role.
Prior experience in cGMP manufacturing operations.
Demonstrated ability to coach and train employees effectively.
Ability to lift up to 50 pounds.
Culture & Benefits
Full-time employment with opportunities for promotion or lateral career development, including international opportunities.
Employee rewards and benefits package including healthcare, prevention and wellness programs.
At least 14 weeks of gender-neutral parental leave.
Work alongside a supportive, future-focused team using digital, data, and AI-driven innovation.
Equal Opportunity and Affirmative Action employer committed to a culturally diverse workforce.
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 →