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Senior Scientist - Analytical Research and Development

93 600 - 156 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Scientist - Analytical Research and Development (Analytical Chemistry/Pharmaceutical Development): Developing analytical strategies, methods, and impurity control approaches for drug substances and products with an accent on chromatography, spectroscopy, mass spectrometry, and stability studies. Focus on solving complex analytical problems, supporting regulatory submissions, mentoring colleagues, and advancing pharmaceutical development in a laboratory environment.

Location: On-premise in Groton, Connecticut, United States. Candidates must have permanent U.S. work authorization; visa sponsorship is not available.

Salary: $93,600–$156,000 annual base salary, plus a 12.5% bonus target and eligibility for a share-based long-term incentive program.

Company

hirify.global is a pharmaceutical research and development company focused on developing medicines and supporting patients worldwide.

What you will do

  • Develop analytical strategies for drug substances and drug products across development phases.
  • Develop, validate, and transfer analytical methods, including methods supporting manufacturing processes.
  • Design stability studies, assign shelf lives, and develop impurity control strategies.
  • Perform laboratory analyses, review peer work, and apply chromatography, spectroscopy, mass spectrometry, particle size analysis, and NMR techniques.
  • Collaborate with multidisciplinary experts, use predictive and modeling tools, and present data while resolving technical challenges.
  • Prepare technical reports and regulatory submission sections, evaluate new instrumentation, and mentor colleagues.

Requirements

  • Ph.D. in Analytical Chemistry or a related field with 0–3 years of relevant industrial experience, or an M.S. with 7–8 years of experience.
  • Ability to meet timelines with minimal supervision and lead multidisciplinary teams.
  • Experience learning new techniques and solving complex analytical problems.
  • Strong oral and written communication, data visualization, reporting, organizational, and multitasking skills.
  • Expertise in one or more relevant methodologies, including chromatography, dissolution, IR/Raman spectroscopy, mass spectrometry, particle size analysis, or NMR.
  • Permanent U.S. work authorization is required; U.S. visa sponsorship is unavailable now and in the future.

Nice to have

  • Pharmaceutical industry experience or experience analyzing peptide therapeutics.
  • Trace-level impurity analysis experience.
  • Experience with global regulatory submissions and separation technologies such as LC, GC, or SFC.
  • Familiarity with LIMS, chromatographic software, Veeva, electronic notebooks, predictive tools, modeling software, or data visualization tools.

Culture & Benefits

  • On-premise laboratory work with some travel and possible lifting requirements.
  • Relocation assistance may be available based on business needs and eligibility.
  • 401(k) with matching contributions and an additional retirement savings contribution.
  • Paid vacation, holidays, personal days, caregiver/parental leave, and medical leave.
  • Medical, prescription drug, dental, and vision coverage.

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