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2 дня назад

Group Leader (RNA Therapeutics)

70 000 - 90 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
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
Group Leader (RNA Therapeutics): Leading a team of scientists and overseeing method establishment and analytical testing for RNA therapeutics, including LNP and AAV methodologies, with an accent on laboratory operations, technical leadership, and GMP-regulated analytical platforms. Focus on developing and validating methods, troubleshooting complex analytical challenges, reviewing data and investigations, and driving corrective and preventive actions.

Location: San Diego, California, USA; candidates must live within a commutable distance. Full-time, Monday to Friday, 8:00 AM–5:00 PM.

Salary: $70,000–$90,000 per year.

Company

hirify.global provides analytical testing and contract research services across food, environmental, pharmaceutical, cosmetic, genomics, and clinical science domains.

What you will do

  • Lead, mentor, recruit, onboard, and develop a team of scientists.
  • Oversee daily laboratory operations, resource scheduling, project milestones, client commitments, quality objectives, turnaround times, and revenue targets.
  • Provide technical leadership for RNA-therapeutic method establishment and routine testing across LC, MS, CE, plate-based assays, DLS/ELS, ELISA, qPCR, ddPCR, and compendial methods.
  • Author and review protocols, test methods, validation documentation, analytical data, investigations, deviations, and laboratory records.
  • Develop technical solutions for complex analytical challenges and support troubleshooting and root cause analysis.
  • Maintain client relationships and communicate project risks, technical challenges, resource constraints, and schedule impacts to stakeholders.

Requirements

  • Bachelor’s degree in chemistry, biochemistry, biology, chemical engineering, or a related field, with at least two years of directly relevant experience; a relevant master’s degree may substitute.
  • Authorization to work indefinitely in the United States without restriction or sponsorship is required.
  • Expertise with HPLC/UPLC, HRMS, and CE for RNA-therapeutic analysis in a GMP-regulated environment.
  • Experience leading laboratory operations, resource planning, analytical method development, and validation.
  • Experience with client communication, technical documentation, peer review of analytical data, and laboratory records.
  • Experience with LIMS is desirable; local or regional candidates are preferred.

Culture & Benefits

  • Collaborative, inclusive, diverse, and results-oriented working environment.
  • Medical coverage with dental and vision options.
  • Life and disability insurance.
  • Paid holidays and vacation.

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