aistatistical analysistechnical writingregulatory filingsgood manufacturing practicesquality by designpharmaceutical formulationsolid dosage forms
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
Нижеразвернуть
$74к-111к/год
$110к$150кмедиана$180к
По похожим ролям (48) ~ $150к/год
77
Хорошая вакансия
развернуть
Чётко описанная роль в известной биотех-компании даёт практический опыт разработки лекарств и сильный пакет льгот, но требует работать в офисе пять дней в неделю.
Ниже рынка
Пять дней в офисе
Понятные задачи
Сильный работодатель
Хорошие льготы
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Formulation Senior Research Associate (Biotech): Developing solid dosage forms for clinical and commercial use in a Quality by Design environment with an accent on formulation optimization, scale-up studies, and regulatory documentation. Focus on interpreting laboratory data, troubleshooting experiments, transferring processes to CMO partners, and supporting GMP-compliant development.
Location: Boston, MA, United States; on-site five days per week with ad hoc flexibility
Base salary: $74,000–$111,000 per year, plus eligibility for annual bonus and equity awards.
Company
Vertex is a global biotechnology company investing in scientific innovation and developing medicines for patients.
What you will do
Develop solid dosage forms for clinical and commercial use and generate data supporting project progression and regulatory filings.
Plan, execute, interpret, and document laboratory experiments for formulation optimization, scale-up, and troubleshooting with minimal supervision.
Maintain complete laboratory notebooks and communicate integrated experimental outcomes through presentations and research reports.
Perform basic statistical analysis and interpret data to form sound conclusions.
Support technical transfer to CMO partners for clinical trial manufacturing.
Contribute to regulatory filing documentation while complying with safety and GMP procedures.
Requirements
Bachelor’s degree in pharmaceutical sciences, chemistry, chemical engineering, materials science, or a related field, plus 4 years of experience in life sciences, engineering, or academia; or a master’s degree in a related field plus 0–2 years of relevant experience.
Technical knowledge of pharmaceutical and engineering principles for solid dosage form development at laboratory, clinical, and commercial scales.
Hands-on experience with formulation techniques, processing equipment, and unit operations at laboratory and clinical manufacturing scales.
Strong mathematics skills, particularly material and energy balances, and intermediate applied statistical analysis skills.
Strong technical writing, verbal communication, and written communication skills.
Ability to multitask efficiently across several concurrent projects, with strong attention to detail.
Strong background in oral solid form development and understanding of material properties.
Nice to have
Direct experience working with contract manufacturing organizations.
Understanding of Quality by Design and experience with regulatory filings.
Culture & Benefits
Continuous learning and encouragement to follow advances in AI, technology, automation, and industry trends.
Medical, dental, and vision benefits, generous paid time off, and company shutdowns during the summer and winter.
Educational assistance programs, including student loan repayment, and a commuting subsidy.
Matching charitable donations, 401(k), and other total rewards supporting financial, family, and wellbeing needs.
Equal employment opportunity, reasonable accommodations, and an inclusive workplace.
Будьте осторожны
Если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого. Это мошенники. Обязательно жмите «Пожаловаться» или пишите в поддержку. Подробнее в гайде →