2 дня назад
Scientist 2 - Pharmaceutical Development
92 600 - 172 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
, 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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