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2 дня назад

Senior Specialist, Analytical Technical Operations (mRNA)

89 900 - 143 800$
Формат работы
hybrid
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 Specialist, Analytical Technical Operations (mRNA): Managing stability studies, analytical testing schedules, and digital operations for novel mRNA and LNP drug candidates with an accent on data interpretation, regulatory support, and scalable laboratory workflows. Focus on integrating laboratory systems, automating analytical operations, coordinating cross-functional programs, and delivering technical data packages for product development decisions.

Location: Norwood, Massachusetts, United States; 70% in-office and 30% remote work model. Only U.S. persons are eligible due to U.S. export-control requirements; hirify.global cannot sponsor non-U.S. persons for an export-control license.

Salary: $89,900–$143,800 annually, with potential eligibility for a discretionary bonus, other incentive compensation, or equity award.

Company

hirify.global develops mRNA-based therapeutics and vaccines using mRNA science, delivery technology, and manufacturing capabilities.

What you will do

  • Develop and maintain integrated analytical testing schedules across CMC Development programs.
  • Author, review, and manage stability protocols and studies for mRNA and lipid nanoparticle drug candidates.
  • Generate, review, trend, and interpret analytical data, including peer reviews, technical summaries, and data packages.
  • Coordinate multiple program timelines, testing milestones, study deliverables, and reporting commitments.
  • Partner with Analytical Development, Process Development, and other CMC functions on forecasting, sample management, and testing strategies.
  • Design digital tools, automated workflows, and laboratory-system integrations that improve analytical operations.

Requirements

  • Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, Chemical Engineering, or a related scientific discipline.
  • 6–8 years of experience in biotechnology, pharmaceuticals, analytical development, technical operations, or CMC Development.
  • Experience managing stability studies, analytical testing programs, or laboratory operations in a regulated environment.
  • Experience with LabVantage, Benchling, or similar LIMS, ELN, and data-management systems.
  • Strong project management, organizational, problem-solving, written, and verbal communication skills.
  • Must qualify as a U.S. person under U.S. export-control laws.

Nice to have

  • Experience with mRNA, LNP, biologics, or other advanced therapeutic modalities.
  • Knowledge of CMC Development, stability programs, IND submissions, and regulatory requirements.
  • Experience with process automation, workflow optimization, data visualization, or digital transformation.
  • Experience leading cross-functional programs involving planning, prioritization, risk mitigation, and milestone execution.

Culture & Benefits

  • 70/30 work model emphasizing in-office collaboration, teamwork, and direct mentorship.
  • Healthcare and voluntary benefit programs.
  • Fitness, mindfulness, and mental-health support.
  • Family-planning benefits, including fertility, adoption, and surrogacy support.
  • Paid vacation, volunteer days, sabbatical, global recharge days, and discretionary year-end shutdown.
  • Savings and investment programs, plus location-specific benefits.

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