Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$75к-113к/год
$88к$95кмедиана$110к
По похожим ролям (49) ~ $95к/год
На СНГ рынке: $1.8к/мес ($1.4к - $3к)
83
Хорошая вакансия
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Обязанности четко определены, а работа дает серьезную ответственность в регулируемом биопроизводстве, но требует присутствия на площадке и участия в работе нескольких смен.
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Работа между сменамиПонятная зона ответственностиБиопроизводствоПоддержка развития
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Supervisor, Manufacturing - DAP (Day Shift) (Biomanufacturing): Leading device assembly and packaging operations to produce high-quality products with an accent on cGMP compliance, employee development, equipment performance, and safe manufacturing. Focus on optimizing production processes, managing deviations and change controls, qualifying new equipment, and driving lean continuous improvement across cross-functional teams.
Location: USA - OH - West Chester
Salary: $75,000–$112,500 per year
Company
hirify.global is a technology-focused biomanufacturing company building sustainable, end-to-end manufacturing solutions for pharmaceutical products.
What you will do
Lead device assembly and packaging process operations across production activities, staffing coordination, scheduling, and improvement initiatives.
Direct employees in the efficient use of equipment and materials while maintaining product quality, safe work practices, cGMP, regulatory, SOX, SHE, and company standards.
Train and develop PET staff on equipment, processes, and SOPs in partnership with Process Leads and Training Coordinators.
Collaborate with OE and PET Engineers to optimize processes and participate in the design, installation, and qualification of equipment, facilities, and processes.
Drive continuous improvement, lean behaviors, performance management, career development, and effective collaboration across PETs and operating shifts.
Requirements
Prior experience in a production environment.
Strong communication, leadership, problem-solving, mechanical, electrical, and troubleshooting skills.
Knowledge or previous experience managing technical programs or projects.
Ability to direct and participate in cross-functional teams.
Experience or working knowledge of cGMP production requirements and FDA or international manufacturing regulations.
Nice to have
Bachelor of Science in Engineering, Pharmacy, a related science, or business.
Experience in a LEAN manufacturing environment.
Working knowledge of LDMS, Microsoft applications, and SAP.
Training or experience in formulation, filling, packaging, validation, technology transfer, or change control.
Project management skills and experience in a cGMP production environment.
Culture & Benefits
Full-time, onsite day-shift role with presence maintained across multiple operating shifts.
Benefits include a 401(k) plan with company match, medical, dental and vision coverage, paid vacation, paid holidays, and other paid leave.
Additional benefits include family-building support, life and disability insurance, tuition reimbursement, and caregiving support.
Annual cash bonus program and performance-focused development opportunities are available.
Sponsorship or support for work authorization, including visas, is not available.
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