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7 дней назад

Principal Research Associate, Analytical Development (mRNA)

89 900 - 143 800$
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
Principal Research Associate, Analytical Development (mRNA): Developing, qualifying, and validating microbiological methods for mRNA-based vaccines and therapeutics with an accent on bioburden, endotoxin, sterility, and environmental monitoring. Focus on troubleshooting method performance, supporting investigations and regulatory questions, transferring methods to QC laboratories, and implementing rapid microbiological technologies.

Location: Norwood, Massachusetts, United States; 100% onsite. Due to U.S. export control requirements, only U.S. persons are eligible, and visa sponsorship is not available.

Salary: $89,900–$143,800 per year, with potential eligibility for discretionary bonus, incentive compensation, or equity.

Company

hirify.global develops mRNA-based medicines, vaccines, and therapeutic technologies.

What you will do

  • Execute microbiological method development, optimization, characterization, qualification, and validation studies.
  • Develop and evaluate methods for bioburden, bacterial endotoxin, sterility, environmental monitoring, and related testing.
  • Plan experiments, analyze data, identify variability, troubleshoot technical issues, and recommend next steps.
  • Author protocols, methods, technical reports, validation documentation, and development summaries.
  • Support investigations, deviations, root-cause assessments, regulatory questions, and cross-functional technical evaluations.
  • Transfer methods to internal and external QC laboratories and evaluate rapid or alternative microbiological technologies and automation.

Requirements

  • M.S. in Microbiology, Biology, Molecular Biology, Biochemistry, Biotechnology, or a related field with 4+ years of relevant experience; or B.S./B.A. with 6+ years of relevant industry experience.
  • Hands-on experience with microbiological methods and analytical method development, qualification, validation, or troubleshooting.
  • Experience with bioburden, bacterial endotoxin, and sterility methods; environmental monitoring experience is desirable.
  • Understanding of method performance, suitability, controls, interference, recovery, variability, and fitness for intended use.
  • Strong data analysis, scientific problem-solving, written and verbal communication, documentation, and data integrity skills.
  • Must qualify as a U.S. person under applicable export control laws; non-U.S. persons cannot be sponsored for an export control license.

Nice to have

  • Experience with rapid or alternative microbiological methods, microbial identification, or related technologies.
  • Experience with mRNA, lipid nanoparticles, vaccines, biologics, or other advanced therapeutic modalities.
  • Familiarity with USP and other applicable compendial and regulatory expectations.

Culture & Benefits

  • Fully onsite work supporting direct collaboration, mentorship, and site-based operations.
  • Competitive healthcare and voluntary benefit programs.
  • Fitness, mindfulness, mental health, family planning, 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 perks.

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