Upstream Process Scientist - Ambr250 (Tues-Sat)
About The Position
The Upstream Process Scientist performs upstream process development for large-molecule products within the API-Proteins group, using the Ambr250 Sartorius system. The role conducts protocol-driven laboratory work, including cell culture and operation of Ambr bioreactors, and supports development and scale-up projects. The position involves organizing records, recording experimental results and maintaining accurate, well-organized laboratory notebooks. The scientist conducts, analyzes, and reports data in accordance with departmental requirements; contributes to technical reports and project objectives; and presents data professionally. The role also assists with general laboratory upkeep, including decontamination and disposal of large-scale cell culture and bioreactor waste. The position requires compliance with cGMP practices, SOPs, and internal documentation requirements, as well as clear and professional communication.
Requirements
- Bachelor’s or Master’s degree in biopharmaceutical, biotechnology, or pharmaceutical studies.
- Broad knowledge of upstream process development and hands-on experience.
- Authorization to work in the United States indefinitely without restriction or sponsorship.
Responsibilities
- Perform upstream process development for large-molecule products within the API-Proteins group using the Ambr250 Sartorius system.
- Conduct protocol-driven laboratory work, including cell culture and running Ambr bioreactors.
- Support laboratory work associated with development and scale-up projects within the API-Proteins area.
- Organize records and capture results in data sheets.
- Contribute to technical reports and work individually and as part of a team to meet project timelines and objectives.
- Assist with general laboratory upkeep and organization, including decontamination and disposal of large-scale cell culture and bioreactor waste.
- Conduct, analyze, and report data in accordance with departmental requirements.
- Record experimental data and maintain accurate, highly organized laboratory notebooks.
- Comply with cGMP practices, appropriate SOPs, and internal documentation requirements.
- Analyze and present data in a professional format.
- Demonstrate clear and professional verbal and written communication.
Benefits
- Comprehensive medical coverage
- Dental and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
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What This Job Offers
Job Type
Full-time
