5 дней назад
Principal Research Scientist II (Parenteral Process Engineering)
141 500 - 268 500$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Principal Research Scientist II (Parenteral Process Engineering): Developing and commercializing parenteral manufacturing processes with an accent on filling-machine technology, process engineering, equipment design, and cGMP requirements. Focus on troubleshooting manufacturing issues, developing small-scale and computational models, evaluating new technologies, and leading cross-functional technical initiatives.
Location: North Chicago, Illinois, United States; onsite role
Salary: $141,500–$268,500 USD per year
Company
discovers and delivers medicines and solutions for serious health conditions across immunology, oncology, neuroscience, and aesthetics.
What you will do
- Provide advanced technical expertise in process engineering and troubleshooting for parenteral manufacturing processes.
- Lead the development and lifecycle management of parenteral manufacturing processes from process design through commercialization and technical support.
- Guide the selection and design of process equipment, including filling machines, mixing systems, and facilities for new or expanding manufacturing sites.
- Provide technical guidance to development and manufacturing teams and lead the resolution of manufacturing issues.
- Support process engineering projects through troubleshooting, small-scale modeling, computational modeling, and technology implementation.
- Represent the parenteral PDS&T organization in cross-functional teams and drive global process improvement initiatives.
Requirements
- Expert knowledge and practical experience in Fill & Finish technology, including machine technology, machine setup, mixing systems, and process development.
- Profound knowledge of quality and regulatory requirements for parenteral pharmaceutical and biopharmaceutical processing and filling equipment.
- Experience with parenteral manufacturing or process development and a solid understanding of pharmaceutical development in a cGMP environment.
- M.Sc. or diploma with 14+ years of relevant experience, or PhD with 8+ years in parenteral manufacturing, process development, process engineering, product quality, analytical sciences, material sciences, or a related field.
- Strong leadership, problem-solving, organizational, interpersonal, and technical communication skills.
- Ability to work independently, manage changing priorities and short lead times, and influence multidisciplinary teams without direct authority.
Culture & Benefits
- Collaboration with global engineering, manufacturing, process development, quality teams, and external partners.
- Paid time off, including vacation, holidays, and sick leave, for eligible employees.
- Medical, dental, and vision insurance for eligible employees.
- 401(k) and eligibility to participate in long-term incentive programs.
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