Manufacturing Changeover Manager - Drug Substance (Biopharma)
Контакты
96 200 - 151 400$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Релокация
US
data analysisteam leadershipleanmanufacturinggmpoperational excellencepharmaceutical manufacturingperformance metricscontinuous improvement
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$96к-151к/год
$120к$140кмедиана$160к
По похожим ролям (50) ~ $140к/год
86
Хорошая вакансия
развернуть
В Company hidden чётко описана руководящая роль в регулируемом биофармацевтическом производстве с возможностью влиять на операционную модель развивающейся площадки; работа только на месте и отсутствие визовой поддержки ограничивают доступность вакансии.
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Только на местеПонятные задачиКрупная биофармаРазвитие площадки
Оценка от Hirify AI
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Manufacturing Changeover Manager - Drug Substance (Biopharma): Planning and leading API and drug-substance turnaround activities for a small-molecule manufacturing facility with an accent on safe, compliant, predictable campaign transitions. Focus on building standardized turnaround models, leading cross-functional teams, applying lean principles, and improving schedule adherence, quality, safety, and cycle time.
Location: Elkton, Virginia, United States; onsite, day shift, 10% travel; domestic relocation listed; visa sponsorship is not available.
Salary: $96,200–$151,400 per year, plus eligible annual bonus and long-term incentive.
Company
hirify.global is a research-intensive biopharmaceutical company developing medicines and health solutions for people and animals.
What you will do
Plan, coordinate, and lead turnaround activities for API and drug-substance manufacturing operations.
Ensure safe, compliant, efficient execution with minimal disruption to manufacturing campaigns.
Develop a standardized turnaround model covering scope, sequencing, staffing, materials, work plans, and disciplined handoffs.
Lead, coach, and develop mechanical, electrical, operations, and facility-operations personnel.
Partner with the Production Lead and cross-functional stakeholders to ensure readiness and effective execution.
Track turnaround KPIs and apply lean, standard work, visual management, and continuous-improvement tools to reduce downtime, rework, variability, and cycle time.
Requirements
Bachelor’s degree required; engineering, operations, manufacturing, chemical engineering, pharmaceutical engineering, or a related technical discipline is preferred, but an engineering degree is not required.
At least 5 years of experience in pharmaceutical, biotechnology, chemical, or another regulated GMP manufacturing environment.
Experience leading turnaround, changeover, shutdown, campaign-transition, or operational-readiness activities.
Experience leading teams and coordinating cross-functional stakeholders in manufacturing.
Strong continuous-improvement mindset and practical understanding of lean principles.
Ability to develop standard work, operating systems, and performance metrics, with a data-driven approach to monitoring and improvement.
Strong knowledge of safe and compliant execution in regulated operations.
Ability to work effectively across Operations, Engineering, Quality, Maintenance, Planning, and EHS; high attention to detail and commitment to operational discipline.
Culture & Benefits
Safe, environmentally responsible, and compliant workplace focused on operational excellence.
Opportunity to help build small-molecule manufacturing expertise and the future operating model for the Elkton site.
Medical, dental, vision, and other insurance benefits for employees and families.
Retirement benefits including 401(k), paid holidays, vacation, compassionate leave, and sick days.
Inclusive environment that values diverse perspectives, respectful challenge, collaboration, learning, and continuous improvement.
Hiring process
Applications are accepted through the hirify.global careers portal.
Accommodation support is available during the application and hiring process.
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