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2 дня назад

Senior Associate Scientist (Mammalian Bioanalytics)

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
Senior Associate Scientist (Mammalian Bioanalytics) (qPCR/ELISA/MSD): Developing, validating, and transferring analytical methods for characterization and release of biologics, with an accent on GMP testing, cell-based assays, and biotherapeutic stability. Focus on performing cell culture and cGMP sample testing, compiling technical documentation, and supporting analytical equipment maintenance in a regulated laboratory.

Location: Onsite in Framingham, Massachusetts, United States

Company

hirify.global is an R&D-driven biopharmaceutical company developing medicines and vaccines through immunoscience and AI-powered research.

What you will do

  • Develop, qualify, validate, and transfer analytical methods including qPCR, ELISA, MSD, and cell-based assays.
  • Perform pre-clinical and clinical lot release and stability testing of antibodies, antibody-like molecules, enzymes, and other biotherapeutics.
  • Carry out cell culture activities such as thawing, passaging, and cell banking.
  • Perform cGMP sample testing according to SOPs and compile data packets.
  • Draft SOPs and technical reports, communicate experimental results, and deliver analytical documentation on schedule.
  • Maintain analytical equipment and support a GMP-compliant laboratory.

Requirements

  • Bachelor’s degree in Biology, Biochemistry, Immunology, Molecular Biology, Cell Biology, or a related discipline with at least two years of relevant biotechnology or pharmaceutical experience, or a Master’s degree with at least six months of experience.
  • Hands-on experience with at least one of ELISA, qPCR, MSD, or cell-based assay techniques.
  • Understanding of biology, biochemistry, and biophysical methods.
  • Ability to work in a fast-paced, collaborative environment, organize work efficiently, and meet timelines.
  • Ability to follow appropriate GMP standards, including investigations of invalid results, deviations, and CAPAs.
  • Proficiency with Microsoft Word, Excel, PowerPoint, and ELN.

Nice to have

  • Laboratory internship or co-op experience.
  • Cross-training or experience with cIEF, CE-SDS, or SEC separation techniques.

Culture & Benefits

  • Opportunity to support life-changing treatments and work across science, medicine, and operations.
  • Cross-functional collaboration and opportunities for development, stretch roles, and internal career moves.
  • Inclusive, high-performing work environment.
  • Eligibility for company employee benefit programs and additional benefits.

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