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7 дней назад

Manufacturing Changeover Manager - Drug Substance (Biopharma)

96 200 - 151 400$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Релокация
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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.
  • Proven leadership, coaching, team-development, planning, prioritization, problem-solving, decision-making, communication, and influencing skills.
  • 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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