6 часов назад
Downstream Process Development Scientist II (Biotech)
106 480 - 146 410$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Downstream Process Development Scientist II (Biotech) (Chromatography and cGMP): Developing, characterizing, and transferring microbial downstream processes to commercial cGMP manufacturing with an accent on chromatography, tangential flow filtration, and regulatory-quality documentation. Focus on leading downstream development programs, optimizing unit operations, supporting technology transfer, and solving process and manufacturing issues.
Location: Boulder, Colorado, United States; onsite laboratory and manufacturing support, including shift coverage as needed.
Salary: $106,480–$146,410 per year
Company
provides biopharmaceutical process development, technology transfer, and cGMP manufacturing services.
What you will do
- Execute downstream process development, process characterization, and technology transfer for microbial processes.
- Design and perform laboratory studies for chromatography, tangential flow filtration, normal filtration, sampling, and basic process-sample analysis.
- Lead the downstream workstream for development, characterization, and technology transfer programs as a subject matter expert.
- Prepare protocols, reports, client documentation, regulatory-quality records, and technical presentations.
- Provide technical support during cGMP manufacturing through floor coverage, batch document review, deviation support, and change controls.
- Evaluate and implement downstream technologies to improve process performance and operational efficiency.
Requirements
- B.S. degree with 6+ years of related experience, M.S. with 4+ years, or Ph.D. with 1+ years in a scientific discipline.
- Required experience in downstream process development and chromatography equipment.
- Strong written and verbal communication skills, customer-service focus, and ability to meet strict client deadlines.
- Collaborative approach and flexibility to support downstream processes and laboratory activities.
- Ability to maintain training compliance and follow departmental safety procedures.
- Knowledge of GMPs and regulations for biotechnology-derived products is preferred.
Culture & Benefits
- Full-time salaried exempt employment.
- Work includes collaboration across laboratory and manufacturing areas.
- Workforce diversity and equal employment opportunity are supported.
- Shift work may be required to meet laboratory and organizational needs.
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