Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$70к-170к/год
$110к$130кмедиана$140к
По похожим ролям (49) ~ $130к/год
На СНГ рынке: $3.1к/мес ($2.5к - $3.5к)
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Обязанности понятны и связаны с капитальными проектами в фармацевтике, но работа на площадке клиента и поездки ограничивают гибкость по месту работы.
Работа на площадке
Понятные задачи
Компания принадлежит сотрудникам
?Узкая специализация
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Process Engineer (Pharmaceutical/cGMP): Executing capital projects and engineering design for pharmaceutical and life sciences facilities with an accent on regulated manufacturing, clean utilities, process equipment, and controlled documentation. Focus on commissioning and qualification, developing PFDs and P&IDs, managing validation and change control, and solving system design challenges involving fluid flow, heat transfer, mass balance, and pressure safety.
Location: Onsite at a client site in Raleigh, NC, United States; travel required based on project needs.
Salary: $70,000–$170,000 annually, plus performance-based bonuses.
Company
hirify.global is an employee-owned engineering and professional services firm providing integrated engineering and consulting services across pharmaceutical, life sciences, healthcare, science and technology, clean energy, infrastructure, and other industries.
What you will do
Execute capital projects for greenfield builds and operating facilities from scope development through implementation, commissioning, qualification, and handover.
Support engineering design, technical documentation, specifications, test plans, and project deliverables.
Coordinate with engineering design, construction management, CQV, and start-up teams.
Manage cGMP-controlled documentation, validation, change control, data analysis, and progress reporting.
Communicate scope, deliverables, risks, and compliance requirements to clients, contractors, suppliers, and project teams.
Create practical solutions, support collaborative innovation, and drive projects forward independently.
Requirements
Bachelor’s degree in engineering; Chemical or Mechanical Engineering preferred.
More than 5 years of experience in the pharmaceutical industry or another relevant regulated industry.
Hands-on experience in cGMP-regulated environments involving clean utilities, process equipment, maintenance/reliability, or manufacturing systems.
Understanding of how engineering activities integrate with controlled documentation, validation, and change control processes.
Experience developing and interpreting PFDs, P&IDs, equipment specifications, system design documentation, and CQV documentation.
Experience supporting capital projects in operating facilities, including system upgrades, expansions, or process improvements.
Working knowledge of fluid flow, heat transfer, mass balance, and pressure safety applied to system design and operation.
Ability to work independently, take initiative, adapt to varied projects, maintain composure under pressure, and build professional relationships.
Candidates without direct pharmaceutical experience must demonstrate transferable experience in regulated manufacturing environments such as critical utility systems, cleanrooms, or process equipment.
Nice to have
FE or PE certification.
Proficiency with engineering tools and software platforms.
Culture & Benefits
Employee-owned organization focused on inspiring, achieving, connecting, and sustainable long-term impact.
Medical, dental, and vision insurance.
401(k) with company match, paid time off, and company holidays.
Wellness programs and employee assistance resources.
Professional development support and performance-based bonuses.
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