1 день назад
Research Associate/Engineer I (mRNA CMC Development)
63 200 - 100 900$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Research Associate/Engineer I (mRNA CMC Development): Developing manufacturing processes for mRNA therapeutics and vaccines through three six-month rotations, with an accent on mRNA synthesis, lipid nanoparticle assembly, formulation, and process development. Focus on scaling up processes, designing experiments, analyzing data, establishing process controls, and supporting technology transfer and manufacturing.
Location: Norwood, Massachusetts; site-based full-time work at ’s facility, not eligible for remote work.
Salary: $63,200–$100,900 per year, with potential bonus, incentive compensation, or equity subject to eligibility.
Company
develops mRNA medicines and vaccines through its mRNA technology platform.
What you will do
- Complete three six-month rotations across CMC Development and contribute to project teams developing manufacturing platforms for mRNA therapeutics and vaccines.
- Generate experimental results, analyze data, and prepare technical reports with conclusions and recommended next steps.
- Design and execute experiments, formal risk assessments, scaled-down models, and high-throughput setups for process unit operations.
- Perform process scale-up, support technology transfer, and provide manufacturing support at internal and external contract manufacturing sites.
- Optimize formulation and processing conditions affecting the stability of mRNA drug products and intermediates.
- Characterize mRNA and lipid nanoparticles with analytical teams and present findings in cross-functional meetings.
Requirements
- Bachelor’s or master’s degree in chemical engineering, biochemical engineering, bioengineering, chemistry, biochemistry, biomedical engineering, biophysics, biostatistics, biotechnology, mathematics, molecular biology, pharmaceutical science, statistics, or a related field.
- Strong scientific and engineering fundamentals for evaluating experimental data.
- Laboratory experience applicable to bioprocess development and analytical methods.
- Must already hold U.S. work authorization and maintain it without future sponsorship.
- Only U.S. persons eligible under export-control requirements: U.S. citizens, permanent residents, asylees, or refugees.
Nice to have
- GPA of 3.5 on a 4.0 scale or equivalent.
- Ability to work independently and contribute to high-performing teams.
- Strong written and verbal communication skills.
- Aptitude for learning GxP regulations, including GMP and GLP.
Culture & Benefits
- In-person culture with a 70/30 work model emphasizing office collaboration, teamwork, and mentorship.
- Healthcare and voluntary benefit programs.
- Fitness, mindfulness, and mental health resources.
- Family planning benefits, including fertility, adoption, and surrogacy support.
- Paid time off, volunteer days, sabbatical, global recharge days, and year-end shutdown.
- Savings and investment programs plus location-specific perks.
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