Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$100к-149к/год
$120к$140кмедиана$160к
По похожим ролям (50) ~ $140к/год
На СНГ рынке: $2.5к/мес ($1.9к - $3.1к)
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Зона ответственности четко очерчена: управление производством в регулируемой среде, командой и улучшением процессов. При этом важно учитывать работу на площадке и высокий уровень ответственности.
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Работа на площадкеЧеткая зона ответственностиБиопроизводство
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
Manager, Manufacturing & Process Execution DAP (Biomanufacturing): Leading DAP line operations in a cGMP-regulated biomanufacturing environment with an accent on production performance, staffing, quality, safety, compliance, and continuous improvement. Focus on resolving complex process problems, developing manufacturing teams, managing deviations and change controls, and optimizing equipment and end-to-end product flow.
Location: West Chester, Ohio, United States; onsite manufacturing role
Salary: $100,000–$148,750 per year base pay, plus an annual cash bonus program.
Company
hirify.global is a technology-focused biomanufacturing company building a sustainable network of high-tech, end-to-end manufacturing solutions.
What you will do
Own daily DAP line performance, including staffing, equipment, materials, schedules, production, quality, safety, and cost targets.
Lead technicians, engineers, Supervisors, and direct reports; set operational goals and manage hiring, performance, training, and career development.
Drive continuous improvement, KPI performance, team-based problem solving, Lean behaviors, and cross-functional product flow.
Partner with MSAT, Engineering, Quality, and adjacent Process Execution Teams to resolve complex process issues and optimize operations.
Support equipment, facility, and process design, qualification, lifecycle management, and capital planning.
Maintain manufacturing documentation and compliance, including SOPs, work instructions, cGMP requirements, deviations, audits, complaints, and change controls.
Requirements
Advanced knowledge of packaging or manufacturing operations in a pharmaceutical, biotechnology, or other cGMP-regulated environment.
Strong leadership, communication, and writing skills, with experience leading and developing direct reports and managing resources, timelines, and priorities.
Ability to lead and influence cross-functional teams on initiatives affecting the DAP operation.
Demonstrated proficiency with Microsoft Office Suite and computer applications.
The preferred experience is 7+ years in pharmaceutical, biotechnology, or cGMP-regulated manufacturing, including supervisory or leadership experience.
Preferred knowledge includes FDA cGMP and applicable domestic and international regulatory requirements, sufficient to serve as a compliance subject-matter expert.
Preferred skills include technical writing, mechanical, electrical, and process troubleshooting, complex problem solving, and Lean manufacturing.
Nice to have
Bachelor’s degree in Engineering, a related science, or Business.
Working knowledge of generative AI language tools such as Claude.
Culture & Benefits
Full-time employment with healthcare, dental and vision coverage, family-building benefits, life and disability insurance, paid vacation, paid holidays, and other paid leave.
Annual cash bonus program and 401(k) plan with a generous company match.
Tuition reimbursement and caregiving support.
Visa and work authorization sponsorship or support is not available.
Employment includes compliance with applicable EHS, regulatory, SOX, cGMP, and hirify.global standards.
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