Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Понятные задачи в области технологического проектирования и сильный пакет льгот делают вакансию привлекательной, но зарплата не раскрыта, а работа требует находиться в Клейтоне без возможности получить спонсорство визы.
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Зарплата не указанаТолько КлейтонПонятные задачиСильный пакет льготФармацевтические проекты
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Process Engineering Consultant (Pharmaceutical Manufacturing): Developing and optimizing pharmaceutical and biotechnology manufacturing processes through conceptual, basic, and detailed design with an accent on process calculations, PFDs, P&IDs, equipment specifications, and GMP compliance. Focus on analyzing technical challenges, sizing equipment, collaborating with multidisciplinary project teams, and supporting implementation in regulated manufacturing environments.
Location: Clayton, North Carolina, United States; must be based in Clayton. Unrestricted authorization to work in the United States is required, and employer-sponsored work authorization is not available.
Company
hirify.global delivers engineering consulting and project solutions for pharmaceutical, biotechnology, and life sciences manufacturing.
What you will do
Develop process engineering deliverables, including process flow diagrams, process descriptions, equipment specifications, calculations, and technical reports.
Execute engineering tasks across conceptual, basic, and detailed design phases while meeting project quality, budget, and schedule expectations.
Collaborate with multidisciplinary project teams, customers, vendors, and subject matter experts to develop practical and compliant process solutions.
Analyze technical challenges, evaluate alternatives, and recommend solutions supporting customer objectives and project delivery.
Contribute to knowledge sharing, process improvements, and best practices.
Requirements
Willingness and ability to be based in Clayton, North Carolina, and work in an agile, fast-paced, project-oriented environment.
Bachelor's or master's degree in Chemical Engineering, Biochemical Engineering, Biotechnology, Pharmaceutical Engineering, or a related engineering discipline.
At least 3 years of relevant engineering experience in pharmaceutical, biotechnology, life sciences, or related regulated industries.
Experience with process calculations, PFDs, P&IDs, equipment sizing, and technical documentation.
Familiarity with GMP-regulated environments and pharmaceutical manufacturing processes.
Ability to collaborate with multidisciplinary teams to solve technical challenges and deliver high-quality engineering solutions.
Strong communication skills and the ability to build productive relationships with customers and project teams.
Proactive mindset, strong attention to detail, commitment to continuous improvement, and willingness to expand technical capabilities through project experience, learning, and feedback.
Unrestricted authorization to work in the United States without current or future sponsorship requirements.
Nice to have
Experience with commissioning, qualification, validation, or process optimization activities.
Culture & Benefits
Collaborative environment with multidisciplinary project teams, customers, and subject matter experts.
Competitive salary with annual adjustment increases.
160 hours of PTO, prorated from the hire date, plus 14 paid holidays.
Health, dental, and vision insurance from day one.
8% guaranteed 401(k) company contribution.
14 weeks of paid parental leave, company-paid life and disability insurance, and employee referral bonuses.
Hiring process
Applications are accepted through the online application system only.
Interviews are conducted on a rolling basis.
Application deadline: November 6, 2026.
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