6 дней назад
Principal Research Scientist II (Biotechnology)
141 500 - 268 500$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Principal Research Scientist II (Biotechnology): Leading the development, lifecycle management, troubleshooting, and commercialization of parenteral manufacturing processes with an accent on fill-finish technology, filling machines, process engineering, and cGMP requirements. Focus on designing process equipment and facilities, developing computational models, resolving manufacturing issues, and driving cross-functional technical initiatives.
Location: North Chicago, Illinois, United States
Salary: $141,500–$268,500 per year
Company
develops medicines and solutions for serious health conditions across immunology, oncology, neuroscience, and aesthetics.
What you will do
- Lead the development and lifecycle management of parenteral manufacturing processes from development through product launch and technical commercial support.
- Provide technical expertise on filling machines, equipment capabilities, process design, and troubleshooting.
- Guide development and manufacturing teams in resolving technical issues and implementing process improvements.
- Support equipment selection and facility design for new or expanding manufacturing sites.
- Develop and apply small-scale and computational process models for development projects.
- Represent Parenteral PDS&T in cross-functional teams and present scientific results to diverse audiences.
Requirements
- Master’s degree or diploma with 14+ years of experience, or PhD with 8+ years of experience, in parenteral manufacturing, process development, process engineering, product quality, analytical sciences, material sciences, or a related field.
- Expert knowledge and practical experience in fill-finish technology, including machine technology, machine setup, mixing systems, and process development.
- Strong knowledge of quality and regulatory requirements for parenteral pharmaceutical and biopharmaceutical processing and filling equipment.
- Understanding of pharmaceutical development in a cGMP environment.
- Demonstrated leadership in establishing and managing cross-functional manufacturing teams.
- Strong problem-solving, organization, communication, and collaboration skills, including the ability to influence without direct authority.
Nice to have
- Practical experience with parenteral fill-finish processes.
Culture & Benefits
- Collaboration with global engineering, manufacturing, process development, quality, and external partner teams.
- Opportunities to evaluate new technologies and lead global initiatives.
- Paid vacation, holidays, and sick leave.
- Medical, dental, and vision insurance.
- 401(k) and eligibility for long-term incentive programs.
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