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6 дней назад

Specialist, Engineering Projects (Vaccine Manufacturing)

87 300 - 137 400$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
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
Specialist, Engineering Projects (Vaccine Manufacturing): Supporting end-to-end technical operations for commercial vaccine manufacturing and packaging with an accent on continuous improvement, GMP compliance, process performance, and equipment support. Focus on leading engineering projects, investigating CAPAs and deviations, resolving complex process and equipment issues, and developing technical documentation and experimental protocols.

Location: West Point, Pennsylvania, United States; onsite, 1st-shift day work. No relocation, travel, or flexible work arrangement.

Salary: $87,300–$137,400 annually, plus potential annual bonus and long-term incentive.

Company

hirify.global develops and manufactures pharmaceutical and vaccine products.

What you will do

  • Provide end-to-end technical support for commercial vaccine manufacturing and packaging operations.
  • Support, execute, and lead continuous improvement, value-capture, CAPA, Right-First-Time, deviation-reduction, yield, efficiency, and cycle-time projects.
  • Manage project timelines, meet compliance requirements and customer deadlines, escalate delays, and develop remediation plans.
  • Collaborate with manufacturing personnel, Quality, Planning, project teams, support functions, and external equipment and component vendors.
  • Investigate root causes across safety, compliance, automation, equipment, process, and personnel considerations, and provide advanced technical support for complex operational issues.
  • Design, conduct, review, and approve experimental protocols; prepare technical and manufacturing documentation; and support regulatory inspections.

Requirements

  • Bachelor’s degree in engineering or another equivalent technical field.
  • At least two years of post-bachelor’s experience in a GMP-regulated functional area or in support of a GMP-regulated function, including Operations, Technical Operations, Technology, Engineering, and/or Maintenance.
  • Experience supporting change control activities and/or project execution.
  • Strong communication, leadership, and teamwork skills.
  • Ability to manage projects and assignments effectively while meeting established schedules and deadlines.

Nice to have

  • Experience serving as a Change Control author and/or reviewer.
  • Experience in biologics, vaccine, bulk sterile manufacturing, or other GMP-regulated manufacturing facilities.
  • Project management experience.

Culture & Benefits

  • Inclusive environment that values diverse experiences, perspectives, skills, and backgrounds.
  • Collaborative culture focused on respectfully challenging ideas and solving problems collectively.
  • Medical, dental, vision, and other insurance benefits for employees and families.
  • Retirement benefits including 401(k), paid holidays, vacation, compassionate leave, and sick days.
  • Reasonable accommodation support is available during the hiring process.

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