About this role
JOB DESCRIPTION:
The Assistant Scientist will play a key role in ensuring successful manufacture of life-saving cell therapy products. The primary focus of the Assistant Scientist will be to support testing and implementation of operational improvements and resolve manufacturing process investigations at the BMS cell therapy GMP manufacturing facilities. The Assistant scientist will be part of a team tasked with completing manufacturing support studies, including investigational, process improvement and process characterization studies. This individual will primarily execute experiments, evaluate data, and draft technical reports. The Assistant Scientist will also contribute to well controlled comparability and validation studies which enable regulatory filings for raw material and process changes.
Primary Responsibilities
Execute experiments in the process development labs which includes aseptic processing and operation of automated process equipment.
Summarize experimental data and aid in analysis to draw conclusions.
Coordinate with the analytical group for timely delivery of process samples and turn-around of analytical data.
Support production related investigations, ensuring compliance with internal standards and regulatory requirements.
Develop and execute manufacturing process changes and improvement activities, and/or author technical reports for process changes and improvements.
Support process comparability and process validation studies including planning, execution, and documentation management. Support necessary technical experiments and analysis to enable decisions related to raw materials changes.
Flexibility with work schedule as maintenance of cell cultures on occasional weekends, early mornings, or evenings is required
Required Qualifications:
Degree in Biological Sciences, Chemical/Biomedical Engineering, Life Sciences or related discipline.
BS degree with minimum of 2+ years of relevant experience, or MS degree with minimum 0+ years of relevant experience in biologic process/analytical development or commercial biologic manufacturing process support.
Excellent documentation skills and attention to detail with cGMP experience a plus.
Ability to effectively work in cross functional teams, meet deadlines, and prioritize responsibilities.
Experience working in a self-driven, performance/results oriented, fast paced matrix environment.
Excellent problem-solving skills.
Able to creatively manage time and elevate relevant issues to project lead and line management.
Strong scientific and technical writing with excellent oral