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2 дня назад

Principal Scientist (Analytical Sciences)

108 000 - 176 000$
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
Principal Scientist (Analytical Sciences): Developing, validating, transferring, and managing analytical methods for siRNA oligonucleotides and peptide therapeutics with an accent on GMP release testing, method lifecycle management, and novel assay technologies. Focus on troubleshooting complex analytical issues, leading OOS/OOT investigations, applying LCMS/MS, CE, and peptide mapping, and aligning QC strategy with CMC and regulatory milestones.

Location: Rensselaer, New York, United States; onsite Monday–Friday, 8:00 a.m.–4:30 p.m.

Salary: $108,000–$176,000 annually

Company

hirify.global is a biotechnology company that discovers, develops, and commercializes medicines for serious diseases.

What you will do

  • Develop, optimize, validate, transfer, and manage analytical methods for raw materials and products, focusing on siRNA oligonucleotides and peptide therapeutics.
  • Design protocols for assay qualification and validation and ensure methods support GMP release testing, characterization, and stability evaluation.
  • Evaluate and implement analytical technologies including LCMS, capillary electrophoresis, ion-pair reversed-phase HPLC, hybridization-based assays, and peptide mapping.
  • Transfer control testing procedures to Quality Control and prepare transfer plans, training materials, and acceptance criteria.
  • Lead troubleshooting, OOS/OOT investigations, deviation root-cause analyses, and customer complaint assessments.
  • Present technical findings, author SOPs and lifecycle documents, mentor junior scientists, and represent Analytical Sciences on cross-functional teams.

Requirements

  • PhD in Chemistry, Biochemistry, Biology, or a related field.
  • 3+ years of relevant industry experience in analytical development and Quality Control method lifecycle management.
  • Demonstrated experience developing and validating methods for siRNA oligonucleotides and peptide therapeutics.
  • Hands-on proficiency with LCMS/MS, capillary electrophoresis, ion-pair reversed-phase HPLC, peptide mapping, and oligonucleotide characterization assays.
  • Experience with method transfer, troubleshooting, OOS/OOT investigations, technical writing, data integrity, and cross-functional collaboration.
  • Ability to work onsite in Rensselaer, New York, Monday–Friday from 8:00 a.m. to 4:30 p.m.

Culture & Benefits

  • Inclusive workplace with equal employment opportunity practices.
  • Comprehensive rewards package that may include annual bonuses, equity awards, retirement benefits, health and wellness programs, insurance, paid time off, and family support benefits.
  • Work is structured around onsite collaboration for many roles.

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