2 дня назад
Late-Stage LNP Process Development Scientist
36 - 41$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Late-Stage LNP Process Development Scientist (LNP drug product manufacturing): Supporting process development, scale-up, and characterization of clinical-stage lipid nanoparticle drug products with an accent on mixing, tangential flow filtration, and in-process analytics. Focus on designing and executing laboratory experiments, analyzing process data, improving process understanding, and documenting science-based manufacturing solutions.
Location: Boston, MA, USA; candidates must live within a commutable distance. Full-time, Monday–Friday, 8:00am–5:00pm, with overtime as needed.
Salary: USD 36.00–41.00 per hour
Company
is an international life sciences company providing analytical testing, laboratory, pharmaceutical, genomics, discovery pharmacology, CDMO, and clinical study support services.
What you will do
- Support process development, scale-up, and process characterization for LNP clinical-stage drug products across 10 mg to 1 gram batch ranges.
- Execute in-process analytics, including dynamic light scattering, UV quantification via Ribogreen, pH, and osmolality.
- Perform laboratory experiments with limited supervision under subject matter expert guidance.
- Organize, analyze, interpret, and present data to process development and cross-functional teams.
- Author SOPs, technical reports, and protocols, and document experiments in electronic lab notebooks such as Benchling.
- Maintain laboratory equipment, order critical reagents, and support operational excellence activities.
Requirements
- B.S. in chemical or biomedical engineering, chemistry, biological sciences, or a related field with 3–4 years of relevant laboratory experience; or an M.S. in biological or biochemical sciences with 1–2 years of relevant experience.
- Experience with bench-scale LNP drug product manufacturing, especially mixing and tangential flow filtration processes.
- Experience with nucleic acid process development, dynamic light scattering, and osmolality monitoring.
- Experience using electronic lab notebooks such as Benchling and preparing SOPs, technical reports, and protocols.
- Strong data analysis, troubleshooting, problem-solving, communication, organization, and time-management skills.
- Authorization to work indefinitely in the United States without restriction or sponsorship is required.
Nice to have
- Experience with UV quantification via Ribogreen.
- Experience with GMP manufacturing practices, tech transfer, T-mixing and TFF.
- Experience with statistical analysis software such as JMP or Design-Expert.
Culture & Benefits
- Collaborative, cross-functional environment focused on science-based manufacturing solutions for complex nucleic acid drug products.
- Professional growth opportunities within the biopharmaceutical industry.
- Medical, dental, and vision coverage, plus life and disability insurance.
- 401(k) with company match, paid vacation and holidays.
- Yearly goal-based bonus eligibility and merit-based increases.
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