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Senior Scientist, Conjugation Process Development (Bioconjugation)

93 600 - 156 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Релокация
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 Scientist, Conjugation Process Development (Bioconjugation): Leading antibody-drug conjugate (ADC) process development projects from early-phase clinical molecules to commercial products with an accent on bioconjugation and protein characterization. Focus on designing and executing scientific studies, optimizing novel processes for cancer-targeting therapies, and facilitating technology transfers.

Location: On Premise in Bothell, Washington, US. Must be authorized to work in the U.S. without visa sponsorship.

Salary: $93,600 – $156,000

Company

Global research-based pharmaceutical company focused on delivering breakthroughs that change patients' lives through advanced science and technologies.

What you will do

  • Lead ADC process development projects from early-phase clinical molecules through late-stage or commercial products.
  • Independently design, execute, and interpret studies to solve defined scientific questions within set timeframes.
  • Facilitate internal and external technology and assay transfers.
  • Author and review technical reports, manufacturing documents, regulatory submissions, and publications.
  • Identify areas for process improvement and propose innovative technology development solutions.
  • Mentor team members and represent the group within multidisciplinary project teams.

Requirements

  • PhD with 0-3 years of experience, Master's with 7-8 years, or Bachelor's with 9-11 years in chemistry, biochemistry, chemical engineering, or a related field.
  • Direct experience with antibodies, proteins, and/or bioconjugation.
  • Strong understanding of analytical protein characterization, including HPLC, IEF, and CE-SDS.
  • Foundational knowledge of organic chemistry, reaction mechanisms, and process development.
  • Permanent work authorization in the United States is required; visa sponsorship is not available.
  • Willingness to work with highly potent cytotoxic molecules and perform complex data analysis.

Nice to have

  • Experience with tangential flow filtration.
  • Proficiency with statistical and data analysis software such as JMP for experimental design and visualization.
  • Experience with GMP manufacturing and familiarity with CMC team functions.
  • Experience with technology transfer to manufacturing.
  • Knowledge of chemical synthesis and protein modification.

Culture & Benefits

  • Comprehensive health benefits including medical, prescription drug, dental, and vision coverage.
  • 401(k) plan with company matching and additional retirement savings contributions.
  • Generous paid time off, including vacation, holiday, personal days, and caregiver/parental leave.
  • Eligibility for the Global Performance Plan with a bonus target of 12.5% of base salary.
  • Participation in a share-based long-term incentive program.

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