3 дня назад
Scientist I, mRNA, Process Development (Biotech)
105 000 - 145 000$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Scientist I, mRNA, Process Development (Biotech): Developing, optimizing, and scaling mRNA synthesis, purification, and characterization processes with an accent on in-vitro transcription, plasmid DNA linearization, chromatography, and tangential flow filtration. Focus on transferring mRNA drug-substance processes from bench scale to GMP manufacturing, supporting mRNA therapeutics projects, and ensuring product quality through analytical characterization.
Location: Waltham, Massachusetts, United States
Salary: $105,000–$145,000 per year
Company
is a technology-driven biotechnology company providing integrated technologies, services, and manufacturing expertise for advanced therapies from design through commercialization.
What you will do
- Lead development, optimization, and scale-up experiments for mRNA production and purification.
- Characterize mRNA samples using electrophoresis, spectrophotometry, HPLC, and UPLC.
- Support tech transfer of mRNA-based therapeutics from process development into manufacturing.
- Collaborate with MSAT, analytical development, external clients, and business development teams.
- Prepare statements of work and proposals, communicate experimental results, and develop SOPs and technical documents.
Requirements
- BS or MS in Microbiology, Bioengineering, Biochemistry, or a related discipline, plus 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 downstream processing, TFF, and chromatography.
- Experience operating ÄKTA Avant/Pure systems and Repligen KrosFlow Kr2i filtration skids.
- Experience with mRNA process technology transfer and scaling from bench scale to GMP manufacturing.
Nice to have
- Experience with mRNA-LNP formulation and mixing technologies.
- 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 within the Process Development department.
- Work with cross-functional teams and external clients on advanced mRNA therapeutics.
- Equal employment opportunity and reasonable accommodations for qualified applicants with disabilities.
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