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2 дня назад

Scientist 2 - Pharmaceutical Development

92 600 - 172 000$
Тип работы
fulltime
Грейд
middle
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
Scientist 2 - Pharmaceutical Development (Biopharmaceutical Process Development): Developing and scaling parenteral drug product processes from laboratory through commercial manufacturing, with an accent on formulation, filling, filtration, freeze/thaw, mixing, sterilization, and lyophilization. Focus on designing small-scale models, executing qualification studies and technology transfers, and solving process challenges across cross-functional development and manufacturing projects.

Location: South San Francisco, California, United States of America

Salary: $92,600–$172,000 annually, plus potential discretionary annual bonus

Company

hirify.global, a member of the Roche Group, develops innovative medicines for serious and life-threatening diseases.

What you will do

  • Develop and support parenteral drug product processes, including freeze/thaw, mixing, filtration, filling, lyophilization, and sterilization.
  • Design small-scale models to understand process mechanisms and reduce scale-up risks.
  • Execute development and qualification studies, technology transfers, and investigations of new technologies.
  • Perform hands-on process development and troubleshooting at laboratory, pilot-plant, and commercial scales.
  • Author, review, and approve technical, development, validation, manufacturing, regulatory, and GMP documentation.
  • Collaborate with formulation scientists, device engineers, manufacturing, quality, regulatory, commercial, and project leadership groups.

Requirements

  • Bachelor’s degree in chemical engineering, pharmaceutical sciences, chemistry, bioengineering, or a related engineering discipline.
  • 2+ years of relevant industry experience.
  • Ability to apply chemical engineering, chemistry, and biology principles to drug product processes.
  • Hands-on experience with protein processing, laboratory techniques, and instrumentation.
  • Strong analytical, problem-solving, written, and verbal communication skills.
  • Knowledge of GMP documentation principles, applicable standards, industry guidance, and regulatory statutes.

Nice to have

  • Biopharmaceutical industry experience.
  • Expertise in large-molecule parenteral drug product process development.
  • Experience implementing processes in a clinical or commercial manufacturing facility.

Culture & Benefits

  • Regular full-time employment with benefits.
  • Potential eligibility for a discretionary annual bonus based on individual and company performance.
  • Relocation benefits are not available for this position.
  • Equal employment opportunity and reasonable accommodation support are provided.

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