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5 дней назад

Process Development Associate (Pharmaceutical Development)

74 503 - 100 799$
Формат работы
hybrid
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
Process Development Associate (Pharmaceutical Development): Developing formulations and manufacturing processes for small-molecule solid oral dosage forms with an accent on process science, digital tools, and data-driven development. Focus on designing experiments, analyzing formulation data, integrating AI-enabled applications, and collaborating with analytical, R&D, and manufacturing teams.

Location: Hybrid in Thousand Oaks, California, United States

Annual salary: $74,503–$100,799

Company

hirify.global is a biotechnology company developing, manufacturing, and delivering medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Research and provide hands-on formulation and process expertise for clinical and commercial small-molecule solid oral dosage forms.
  • Design and develop digital tools and applications for synthetic drug product workflows, including AI-driven interfaces and calculation tools.
  • Collaborate with analytical, R&D, manufacturing, Drug Product Technologies, and external functions to resolve technical challenges and advance projects.
  • Design and execute experiments, analyze and interpret data, and support formulation and process decisions.
  • Contribute to scientific review papers, technical guidelines, literature research, and experimental validation.
  • Organize and communicate technical information to support drug development programs and cross-functional initiatives.

Requirements

  • Master’s degree or foreign equivalent in bioengineering, pharmaceutical sciences, chemical or pharmaceutical engineering, chemistry, life sciences, or a related field, plus a university course, research project, internship, thesis, or one year of experience.
  • Knowledge of unit operations and formulation principles for oral solid dosage forms and pharmaceutical manufacturing processes.
  • Programming proficiency in Python, R, or MATLAB, with experience developing or enhancing AI-driven digital tools and user interfaces.
  • Experience with GMP-compliant manufacturing operations under established SOPs.
  • Experience with Figma, Power BI, IMARIS, GraphPad Prism, Excel, statistical analysis, market research, literature review, and experimental design.
  • Experience using ELN systems to track experiments and support data integrity and knowledge sharing.

Culture & Benefits

  • Collaborative, innovative, and science-based work environment.
  • Medical, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Annual bonus program and stock-based long-term incentives, subject to eligibility.
  • Paid time-off plans, work-life balance support, and career development opportunities.
  • Flexible work models, including hybrid and remote arrangements where possible.

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