qapower bisapgmpprocess engineeringroot cause analysischange controlcapa
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Выше рынка
$94к-108к/год
$83к$90кмедиана$100к
По похожим ролям (50) ~ $90к/год
На СНГ рынке: $1.4к/мес ($1.1к - $1.8к)
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Роль четко описана, а зарплата выше рыночной. Единственный нюанс - найм идет через агентство, а не напрямую в компанию, что может влиять на долгосрочную стабильность.
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Работа через агентствоВысокая зарплатаПонятный функционалСтабильный доменАктуальный стек
Оценка от Hirify AI
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Industrial Process & Quality Engineer (GMP/Manufacturing): Investigating production deviations, authoring technical documentation, and improving manufacturing processes with an accent on compliance, root cause analysis, and Right-First-Time performance. Focus on troubleshooting equipment and automation issues, validating process improvements, and managing CAPA and change-control projects against critical deadlines.
Location: West Point, Pennsylvania, United States; onsite production environment
Salary: $93,600–$108,200 per year
Company
hirify.global provides staffing and employment services for technical and engineering roles.
What you will do
Lead investigations into operational deviations, assess product impact, identify root causes, and define corrective and preventive actions.
Author and maintain SOPs, batch records, change-control documents, and validation protocols.
Provide on-floor technical troubleshooting for process, equipment, automation, safety, and human-factor issues.
Manage continuous-improvement projects, experimental protocols, and pilot studies to improve efficiency, cost, and consistency.
Partner with Operations, Quality, Maintenance, and Regulatory teams to maintain GMP compliance.
Requirements
Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline.
Two to four years of professional experience in manufacturing or a technical production environment; relevant co-op or internship experience is considered.
Strong technical writing, communication, and project-management skills.
Experience with deviation management, root cause analysis, and change control.
Ability to work in a high-paced production environment and provide on-floor technical support.
Nice to have
Experience with SAP or Power BI.
Background in highly regulated manufacturing, such as medical devices, specialized chemicals, or high-complexity consumer goods.
Culture & Benefits
High-stakes, collaborative production environment focused on safety, compliance, and continuous improvement.
Temporary assignments lasting 13 weeks or longer may include medical, dental, vision, 401(k), and statutory sick pay where required.
Reasonable accommodations are available during the employment process.
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