Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Очень мало
$80к-108к/год
$120к$150кмедиана$170к
По похожим ролям (50) ~ $150к/год
65
Средняя вакансия
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Это стабильная позиция в крупной биотехнологической компании, однако предлагаемая зарплата существенно ниже рыночной медианы для данного уровня, что снижает привлекательность предложения.
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Низкая зарплатаРабота в офисеСтабильная отрасльЧеткие задачи
Оценка от Hirify AI
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Process Development Senior Associate (Oral Solid Dosage Forms): Developing oral solid dosage forms for early-stage clinical programs through formulation and process experiments, data analysis, and cross-functional collaboration with an accent on blending, dry granulation, compression, powder characterization, and GMP documentation. Focus on designing and interpreting experiments, evaluating product quality and process performance, improving development tools, and supporting scale-up and technology transfer.
Location: On site in Thousand Oaks, California, United States
Salary: $80,044.50–$108,295.50 annual base salary
Company
Biotechnology company developing, manufacturing, and delivering medicines across oncology, inflammation, general medicine, and rare disease.
What you will do
Develop oral solid dosage forms for early-stage clinical programs through formulation and process development experiments.
Execute key unit operations including blending, dry granulation, and compression, and evaluate their impact on product quality and performance.
Plan and perform material and powder characterization studies, contribute to experimental design, and analyze results to guide development decisions.
Document experiments, data, and conclusions in electronic laboratory notebooks in compliance with GMP requirements and internal SOPs.
Collaborate with Drug Product, Drug Substance, and other cross-functional teams; communicate findings through technical presentations and written reports.
Evaluate process performance and product quality, improve team tools and systems, and support scale-up and technology transfer activities.
Requirements
Master’s degree, or a Bachelor’s degree with 2 years of formulation laboratory experience, or an Associate’s degree with 6 years of formulation laboratory experience, or a high school diploma/GED with 8 years of formulation laboratory experience.
Ability to independently execute experiments and translate results into actionable insights.
Ability to contribute to experimental design and process optimization.
Working knowledge of pharmaceutical development in a GMP environment.
Ability to manage multiple priorities while maintaining attention to detail.
Strong written and verbal communication skills.
Nice to have
Degree in Pharmaceutical Sciences, Material Sciences, Bioengineering, Chemistry, Chemical Engineering, or another relevant field.
2+ years of pharmaceutical industry experience with an emphasis on oral solid dosage forms.
Hands-on experience developing oral solid dosage forms, including blending, dry granulation, and compression.
Experience with powder and solid dosage form characterization techniques.
Experience supporting or developing SharePoint platforms, data tracking tools, knowledge repositories, workflow tracking tools, or other knowledge management systems.
Culture & Benefits
Collaborative, innovative, and science-based work environment.
Health, dental, and vision coverage, life and disability insurance, and flexible spending accounts.
Retirement and savings plan with company contributions.
Discretionary annual bonus program and stock-based long-term incentives.
Award-winning time-off plans and career development opportunities.
Sponsorship for the role is not guaranteed.
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