11 часов назад
Scientist, Process Development (mRNA)
105 000 - 145 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Scientist, Process Development (mRNA) (mRNA therapeutics): Developing and scaling mRNA production and purification processes with an accent on in-vitro transcription, chromatography, filtration, and product characterization. Focus on tech transfer, GMP manufacturing scale-up, and optimizing processes for yield and purity.
Location: Waltham, Massachusetts, United States
Salary: $105,000–$145,000 per year
Company
is a technology-driven biotechnology company developing advanced therapies through integrated technologies, end-to-end services, and manufacturing expertise.
What you will do
- Lead development, optimization, and scale-up experiments for mRNA production processes.
- Characterize mRNA samples using electrophoresis, spectrophotometry, and HPLC/UPLC.
- Collaborate with MSAT, analytical development, and external clients on mRNA therapeutic projects.
- Support business development by preparing statements of work and proposals for external clients.
- Communicate experimental results and project progress to internal and external stakeholders.
- Contribute to SOPs and technical documentation.
Requirements
- BS or MS in Microbiology, Bioengineering, Biochemistry, or a related discipline, with 8+ years of relevant experience.
- At least 4 years of experience working with mRNA-based therapeutics.
- Hands-on experience with in-vitro transcription, plasmid DNA linearization, mRNA processing, TFF, and chromatography.
- Experience operating ÄKTA Avant/Pure chromatography systems and Repligen KrosFlow Kr2i filtration skids.
- Strong understanding of tech transfer for mRNA drug substance production and process scaling from bench scale to GMP manufacturing.
- Work location: Waltham, Massachusetts, United States.
Nice to have
- Experience with mRNA-LNP formulation and mixing technologies or equipment.
- Experience using JMP for Design of Experiments and data analysis.
- Familiarity with GMP regulations, Quality by Design principles, and regulatory filing documentation.
Culture & Benefits
- Regular employment with .
- Equal employment opportunity and reasonable accommodations for qualified individuals with disabilities.
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