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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$72к-113к/год
$80к$88кмедиана$100к
По похожим ролям (48) ~ $88к/год
На СНГ рынке: $1.4к/мес ($1.1к - $1.6к)
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Хорошая вакансия
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Роль чётко связана с автоматизацией GMP-производства в крупной фармацевтической компании, но дежурства по вечерам и выходным могут влиять на баланс работы и личной жизни.
Дежурства вне смены
Фармацевтическое производство
Понятные задачи
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Associate Specialist, Manufacturing Automation (Pharmaceutical Manufacturing): Supporting automation systems for GMP vaccine manufacturing at the West Point site with an accent on process control, troubleshooting, change controls, and compliant operations. Focus on investigating automation incidents, implementing corrective actions, and supporting reliable 24/7 manufacturing systems.
Location: West Point, Pennsylvania, United States; on-site support for manufacturing operations, including off-shift, weekend, and evening coverage as required.
Salary: $71,900–$113,200 per year, plus potential annual bonus and long-term incentive.
Company
hirify.global develops and manufactures pharmaceutical and vaccine products for customers and patients worldwide.
What you will do
Provide automation system support for GMP manufacturing processes and vaccine production.
Support automation components and manufacturing activities on the shop floor.
Design, implement, test, and close change controls for corrective actions and continuous improvement.
Investigate automation incidents and technical issues, implement corrective actions, and prevent recurrence.
Collaborate with Manufacturing, Quality, Engineering, and business stakeholders.
Monitor emerging automation technologies and recommend appropriate adoption.
Requirements
BS in Engineering, Computer Science, or a related field, or a high school diploma with 2 years of GMP manufacturing and/or manufacturing automation experience.
Strong verbal and written communication and interpersonal skills.
Ability to work effectively in a team while managing individual responsibilities.
Ability to comply with global policies, procedures, regulatory requirements, cGMP, safety, and environmental regulations.
Nice to have
Experience in the pharmaceutical or biotechnology industry.
Knowledge of or experience with process control systems.
Experience supporting aseptic processing or sterile manufacturing operations.
Technical and operational experience with computer systems, automation technologies, and programming.
Culture & Benefits
Collaborative and respectful work environment with interaction across functional groups.
Regular employee status with medical, dental, vision, insurance, retirement, 401(k), paid holidays, vacation, compassionate leave, and sick days.
First-shift daytime schedule; approximately 10% travel.
Flexible work arrangements are not applicable, and relocation is not provided.
Visa sponsorship is not available.
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