8 дней назад
Senior Associate Scientist Purification Process Development (AAV)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Associate Scientist Purification Process Development (AAV) (Viral Vector Purification): Developing and scaling robust AAV and non-viral vector purification processes for gene therapy manufacturing with an accent on chromatography, filtration, process optimization, and technology transfer. Focus on designing purification experiments, troubleshooting complex downstream operations, analyzing process data, and transferring processes to manufacturing and CDMO partners.
Location: Waltham, Massachusetts, United States; onsite
Company
is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines through immunoscience, advanced data, and digital technologies.
What you will do
- Develop, design, and conduct viral vector purification experiments for AAV and non-viral vector programs.
- Optimize purification conditions, screen media, troubleshoot experiments, and evaluate new technologies to improve yield and process understanding.
- Apply chromatography, filtration, tangential flow filtration, UF/DF, virus clearance, and inactivation operations across relevant scales.
- Support scale-up and manufacturing process implementation, including technology transfer, gap analyses, and risk assessments with internal teams and CDMOs.
- Analyze data, prepare technical reports and presentations, and contribute to manuscripts and patent applications.
- Build cross-functional collaboration and represent the purification process development team internally and externally.
Requirements
- Bachelor’s or master’s degree in chemical engineering, biological or life sciences, or a related field.
- Bachelor’s degree holders need 2+ years of laboratory or related experience; master’s degree holders need 6+ months. Academic and research experience is accepted.
- Knowledge of purification technologies, chromatography principles, separation methods, and downstream unit operations.
- Experience with GLP and detailed laboratory documentation, technical report writing, and learning new viral vector analytical methods.
- Ability to work under minimal supervision, communicate effectively, build cross-functional relationships, and stand at laboratory bench equipment for extended periods.
Nice to have
- Experience with AAV or non-viral vector purification and large-scale manufacturing operations.
- Knowledge of spectrophotometry, ELISA, HPLC, and SDS-PAGE.
- Familiarity with Quality by Design and Design of Experiments for downstream development.
- Experience with virus clearance studies, technology transfers, biosafety level 2 laboratories, gap analyses, and risk assessments.
Culture & Benefits
- Supportive, collaborative, and future-focused R&D environment.
- Opportunities for career growth through promotion or international and lateral moves.
- Health, wellbeing, and prevention programs with high-quality healthcare benefits.
- At least 14 weeks of gender-neutral parental leave.
- Work with AI, data, and digital platforms to advance drug discovery and gene therapy development.
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