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6 дней назад

Associate Scientist, Downstream Processing (Biotherapeutics)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
Associate Scientist, Downstream Processing (Biotherapeutics): Developing and characterizing purification processes for protein therapeutics with an accent on high-throughput chromatography, filtration, product quality, and recovery. Focus on executing bench-scale experiments, supporting process scale-up and technology transfer, and analyzing data for early-phase biotherapeutic development.

Location: Malvern, Pennsylvania, United States of America; onsite

Company

Johnson & Johnson develops healthcare, Innovative Medicine, and MedTech solutions, including biotherapeutic treatments and medical technologies.

What you will do

  • Develop and apply high-throughput purification strategies for early-phase biotherapeutics, including monoclonal, bispecific, and multispecific antibodies and bioconjugates.
  • Execute bench-scale chromatography and filtration experiments focused on product quality attributes, recovery, and manufacturing fit.
  • Support process characterization, scale-up, and technology transfer for downstream unit operations.
  • Collaborate with upstream, analytical development, formulation sciences, and manufacturing organizations.
  • Author and review technical and regulatory documents while maintaining accurate experimental records.
  • Follow cGLP, safety, environmental, EHSS, and company documentation requirements.

Requirements

  • Bachelor’s degree in Chemical Engineering, Biochemistry, Biotechnology, or a related discipline with 0–5 years of relevant experience, or a master’s degree with 0–3 years of relevant experience.
  • Familiarity with protein purification, bioprocessing, or related scientific methods.
  • Basic understanding of experimental design, execution, and analysis.
  • Strong written and verbal communication, organization, and problem-solving skills.
  • Ability to work independently with limited supervision and collaboratively in a team.
  • Proficiency in Microsoft Excel, Word, and PowerPoint.

Nice to have

  • Understanding of statistical experimental design and DoE methodology.
  • Hands-on experience with ÄKTA fast protein liquid chromatography systems.
  • Experience with chromatography, depth filtration, tangential flow filtration, UFDF, SDS-PAGE, or UV/Vis methods.
  • Experience with JMP, Minitab, or related statistical design software.

Culture & Benefits

  • Work within Innovative Medicine on treatments and cures for complex diseases.
  • Collaborate across scientific, analytical, formulation, and manufacturing functions.
  • Inclusive work environment with equal employment opportunity and applicant accommodation support.

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