What are the responsibilities and job description for the Downstream MSAT Scientist position at VINTABIO, INC.?
Title: Downstream MSAT Scientist
Report: Senior Scientist or Principal Scientist
Location: Philadelphia, PA
Position Type: Full Time, Exempt
Travel: Occasional (0-10%)
Company Summary
VintaBio is a technology company focused on simplifying AAV and lentivirus production. Our custom research and development approach is designed to integrate into services, including platform bridging, GLP toxicology material, and GMP manufacturing. Our research core produces high-yield and world-class POC vectors. Through a comprehensive production workflow that utilizes VintaBio's proprietary cell lines and transfection reagents, we expedite the path to the clinic, offer more reliable manufacturing, and improve economics.
Position Summary
This position is part of the Manufacturing Science & Technology (MSAT) team responsible for VintaBio technology development, process development, and both non-GMP and GMP manufacturing. A Downstream Scientist is a mid-level individual with an understanding of cell/molecular biology and previous experience in downstream biopharmaceutical processing. A Scientist is responsible for hands-on execution of experiments and production batches, as well as authoring experimental protocols, SOPs, and batch documents. A Scientist is expected to independently complete objectives given by Senior/Principal Scientist, serve as a role model to junior scientists, collaborate cross-functionally, and provide support with any other technology, process development, and manufacturing needs.
Key Responsibilities
To perform in this position successfully, an individual must be able to perform each key responsibility satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Other duties may be assigned to meet business needs.
- Independently contribute to technology/process development and manufacturing activities for downstream bioprocessing, ensuring delivery in alignment with VintaBio strategy
- Support Senior/Principal Scientist with experimental design, execution and data analysis, effectively communicating technical results to management
- Author protocols, SOPs, and batch documents to ensure the successful execution of activities related to technology development, process development, and both non-GMP and GMP manufacturing
- Perform as a Subject Matter Expert on a cross-functional team to execute client projects
- Work closely with suppliers and other partners to drive forward technology development initiatives
- Serve as a good financial steward to the Manufacturing Science and Technology team at VintaBio and help to implement budgetary adherence and financial governance
- Coach and train junior scientists/employees on activities and documentation related to technology development, process development, and both non-GMP and GMP manufacturing team operations.
- Other related duties as assigned.
Education and Experience
- Minimum Bachelor’s degree in Chemical or Biological Engineering, Biotechnology, Biology, Biochemistry, or other related field. Master’s preferred.
- 1 - 2 years of industry or academic experience in combination with Bachelor’s or Master’s degree.
Knowledge, Skills and Abilities
- Previous experience in chromatography is required
- Experience with methodologies used for downstream viral vector production in either industry or academia
- Experience in experimental design, execution, and data analysis
- Excellent communication, collaboration, and technical writing skills
- Innovative and creative mindset, with problem solving capabilities
- Proficient in Microsoft Office products.
Physical Requirements
- Ability to lift and carry up to 30lbs
- Ability to sit and stand for extended periods
- Excellent manual dexterity and ability to perform repetitive movements with fingers/hands
Other Physical Requirements: PPE and gown training will be required as this individual will be required to enter into Laboratory and Cleanroom areas.
Work Environment: Work is performed primarily onsite in Philadelphia. 50% or more of the time, this role is in the laboratory.
