5 дней назад
Principal Scientist I, Chemistry
124 500 - 236 500$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Principal Scientist I, Chemistry (Pharmaceutical Manufacturing Development): Conducting late-stage development and commercialization of small-molecule therapies through registration, manufacturing transfer, and product lifecycle activities with an accent on organic chemistry, process characterization, scale-up, and CMC documentation. Focus on designing laboratory experiments, leading cross-functional process development teams, solving complex manufacturing challenges, and supporting regulatory and commercial manufacturing strategies.
Location: North Chicago, Illinois, United States; onsite
Salary: $124,500–$236,500 per year
Company
develops medicines and healthcare solutions across areas including immunology, oncology, neuroscience, and aesthetics.
What you will do
- Lead or contribute to cross-functional teams developing manufacturing processes for small-molecule therapies.
- Design and execute laboratory experiments supporting process development, characterization, scale-up, and commercial manufacturing.
- Define project strategies, responsibilities, timelines, and scientific approaches.
- Act as a subject-matter expert for manufacturing processes and collaborate with manufacturing, regulatory, quality, engineering, analytical chemistry, and solid-state science groups.
- Author and review technical reports, batch records, CMC regulatory documents, publications, presentations, and patents.
- Generate scientific proposals, evaluate emerging technologies and competitive developments, and mentor or supervise colleagues when needed.
Requirements
- Bachelor’s degree with typically 14+ years of experience, master’s degree with typically 12+ years, or PhD with typically 6+ years in organic chemistry.
- Experience in pharmaceutical manufacturing process development and scale-up.
- Expertise in modern organic chemistry, mechanistic understanding, compound purification, and control strategy development.
- Experience with standard analytical methods and tools including HPLC, UPLC, LC-MS, and NMR.
- Demonstrated success in scientific communication, publications, presentations, or patent invention.
- Strong collaboration, communication, and cross-functional leadership skills, with adherence to safety and GxP standards.
Culture & Benefits
- Work in a cross-functional, matrixed environment focused on innovative medicines.
- Collaborate across scientific, manufacturing, regulatory, and quality disciplines.
- Operate within a learning-oriented environment that supports experimentation and innovation.
- Follow corporate standards for safety, controlled materials, conduct, and GxP compliance.
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