- Expiry Date: 11 December 2021
Performs routine cell culture experiments per written procedures, where ability to recognize deviation from accepted practice is required.
Assists in design and creation of material testing plans, identifying critical process parameter and handling troubleshooting
Performs data analysis in order to establish criticality for processes, presents study data and results in team meetings
Author timely reports detailing experimental work and summarizing results, maintaining electronic laboratory notebooks
Assists with the revision and creation of process documents, such as SOPs and electronic work instructions
Collaborate with others to handle day to day operation of the laboratory to ensure smooth operation.
Maintains laboratory space to comply with regulatory requirements and safe work environment
Works in teams and has continual interaction with internal as well as external teams throughout the production process in order to exchange information regarding the run(s) in process.
Experience with aseptic processing of mammalian or primary cell culture in biological safety cabinet
Excellent documentation and data management skills
Detail oriented with excellent verbal and written communication skills
Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web-based applications.
Demonstrated ability to work well both independently and on a team in a fast-paced environment, and prioritize work across multiple projects
Experience scientific writing and executing process development experimental plans and technical reports
Experience with JMP or R for statistical analysis, experimental design, and presentation of experimental results
Experience working in, or exposure to, GMP setting, especially using Good Documentation Practices
B.S. in Chemical/Biological Engineering, Immunology, Biology or relevant scientific discipline with 0-2 years of biotechnology or cell therapy industry experience
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