six sigmalean manufacturingchemical engineeringfmeahazopstatistical process controlprocess validationcgmpchemical manufacturingtech transfer
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$100к-130к/год
$110к$130кмедиана$150к
По похожим ролям (50) ~ $130к/год
На СНГ рынке: $3.1к/мес ($2.5к - $3.5к)
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У роли понятный фокус на технологических процессах в биопроизводстве и конкретные задачи по валидации, трансферу и оптимизации; при этом важно учитывать работу на производстве и обязательные поездки.
?Работа на производстве
Перспективная отрасль
Понятные задачи
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Process Engineer II (Chemical Manufacturing): Leading tech transfer, equipment and process validation, and scale-up for chemical manufacturing processes with an accent on process safety, quality, and data-based optimization. Focus on developing process flow diagrams and risk assessments, investigating deviations, and improving production processes through statistical process control.
Location: Marlborough, MA, United States of America; onsite duties in the office and on the production floor, with required travel
Salary: $100,000–$130,000 per year, plus potential bonus, commission, and equity
Company
hirify.global is a life sciences company developing, producing, and commercializing high-value consumables used to manufacture biological drugs.
What you will do
Lead installation and operational qualification of process equipment and process validations (IQ/OQ/PQ) for new product introduction and technology transfers.
Support new chemical processes by creating process flow diagrams, mass and energy balances, HAZOPs, and FMEAs.
Develop and execute work instructions.
Provide technical support for process deviations, investigations, and corrective actions.
Drive data-based process improvements, scale-up, and optimization.
Promote safety and quality across cross-functional manufacturing activities.
Requirements
Bachelor’s degree or higher in Chemical Engineering or a related field.
5+ years of experience in a related field, including experience in chemical manufacturing.
Knowledge of process and equipment validation, ISO standards, risk assessments, deviation investigations, and change control.
Knowledge of current Good Manufacturing Practices (cGMP).
Understanding of statistical tools and statistical process control.
Strong communication, leadership, technical, and operational skills, with the ability to work cross-functionally.
Safety-first mindset.
Nice to have
Lean manufacturing and Six Sigma knowledge.
Culture & Benefits
Collaborative, highly motivated environment focused on bioprocessing and the production of biologic drugs.
Full-time role involving close collaboration with manufacturing-floor employees and other departments.
Paid time off, health, dental, and vision insurance.
Retirement benefits and flexible spending accounts.
Eligible employees may participate in variable cash programs; eligible roles may receive equity.
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