Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$101к-145к/год
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Это четко очерченная senior-роль на стыке инноваций в производстве мРНК и масштабирования процессов в крупной биофармацевтической компании; обязанности конкретны, а среди преимуществ есть возможности карьерного роста.
Перспективное направление
Четкие задачи
Карьерные возможности
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
BioProcess Engineer (mRNA): Evaluating and integrating technologies for mRNA process development and manufacturing with an accent on scale-up, process intensification, GMP compliance, and technology transfer. Focus on developing next-generation mRNA platforms, transitioning laboratory processes to clinical and commercial manufacturing, and coordinating cross-functional innovation initiatives.
Location: Waltham, Massachusetts, United States; hybrid. Applications are limited to US and Puerto Rico residents.
Salary: $100,500–$145,166.66 annually.
Company
hirify.global is an R&D-driven biopharma company developing medicines and vaccines through immunoscience, AI, data, and digital platforms.
What you will do
Evaluate and integrate emerging technologies for mRNA process development and manufacturing, including proof-of-concept studies and technology roadmaps.
Lead process intensification to improve efficiency, yield, and quality while reducing process steps and waste.
Develop scale-up models and strategies for transitioning processes from laboratory to clinical and commercial manufacturing.
Collaborate with technology providers, academic partners, Manufacturing, and Quality teams while maintaining GMP compliance.
Conduct risk assessments, quantify effects on performance metrics and cost of goods, and lead technology transfers.
Requirements
Bachelor’s, Master’s, or PhD degree in Chemical Engineering, Bioprocess Engineering, Biochemical Engineering, or a related technical field.
Relevant industrial experience in bioprocess engineering or related fields: 5+ years with a BS, 4+ years with an MS, or 2+ years with a PhD.
Demonstrated success implementing new technologies in bioprocess environments with measurable outcomes.
Experience scaling processes from laboratory to clinical or commercial manufacturing.
Strong understanding of bioprocess engineering principles, unit operations, and process development in GMP environments.
Excellent project management, cross-functional leadership, influence, problem-solving, and communication skills.
Excellent spoken and written English.
Nice to have
Knowledge of regulatory requirements for process changes and technology implementation.
Background in modeling, data analysis, or automation.
French language skills.
Culture & Benefits
Supportive, future-focused environment with opportunities for promotion or lateral career moves.
Rewards package and employee benefits, including healthcare, prevention, and wellness programs.
At least 14 weeks of gender-neutral parental leave.
Work on AI, data, and digital platforms supporting drug discovery and development.
Equal Opportunity employment and a culturally inclusive workforce.
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