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2 дня назад

Senior Associate Scientist - Chemistry, Analytical R&D

68 600 - 114 300$
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 Associate Scientist - Chemistry, Analytical R&D (Pharmaceutical Analytics): Supporting drug release and stability testing through analytical characterization of pharmaceutical substances and products with an accent on chromatography, spectroscopy, dissolution, and GMP documentation. Focus on running analytical methods, troubleshooting instruments, analyzing data, and preparing submission-ready documentation for clinical supplies and period extensions.

Location: On premise in Groton, Connecticut, United States. Relocation support may be available based on business needs and eligibility. Permanent work authorization in the United States is required.

Annual base salary: $68,600–$114,300, plus eligibility for a 7.5% bonus target.

Company

hirify.global is a pharmaceutical research and development company focused on developing medicines and vaccines that improve patients’ lives.

What you will do

  • Perform laboratory work supporting analytical testing of pharmaceutical projects.
  • Run analytical methods and test raw materials, drug substances, and finished drug products for clinical release and use-period extensions.
  • Apply chromatography, Karl Fischer, spectroscopy, and dissolution techniques to support physical and chemical characterization.
  • Document experimental results, perform data analysis, and maintain electronic laboratory records.
  • Collaborate with drug substance and drug product project teams, quality assurance, and regulatory CMC on investigations, release, and clinical supply activities.
  • Operate software and information systems while meeting project milestones and timelines.

Requirements

  • BA/BS with at least 3 years of experience, or MBA/MS with any years of experience.
  • Ability to meet project milestones under general supervision, manage project expectations, and deliver submission-ready data and documentation.
  • Experience with problem-solving and instrument troubleshooting.
  • Strong oral and written communication skills, including adherence to laboratory GMP notebook practices.
  • Experience with software and information systems such as electronic lab notebooks, OneLab, CisPro, Empower, and LIMS.
  • Ability to work in a GMP laboratory environment, perform experiments safely, analyze data, record results electronically, and collaborate effectively in a team.
  • Strong documentation, organizational, multitasking, interpersonal, and communication skills with high attention to detail.

Nice to have

  • Pharmaceutical industry experience.
  • Experience working in a regulated environment.
  • Experience with chromatography techniques including HPLC, GC, and HPLC-MS.
  • Experience using AI tools, including ChatGPT or Microsoft Copilot, for problem solving and productivity.
  • Curiosity about responsible AI practices, risk management, and ethical use.

Culture & Benefits

  • On-premise work in a multidisciplinary, fast-paced GMP laboratory environment.
  • Full-time employment with paid vacation, holidays, personal days, and caregiver, parental, and medical leave.
  • Benefits include medical, prescription drug, dental, and vision coverage.
  • 401(k) plan with hirify.global matching contributions and an additional retirement savings contribution.
  • Participation in hirify.global’s Global Performance Plan with a 7.5% bonus target.

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