CSL
Description
The Scientific Associate will be reporting to the Associate Director of the Process Science & Development team within the Biopharmaceutical Process Development organization. The Scientific Associate hired for this position will support development of sa-mRNA and lipid nanoparticle production processes. The scope will include support of process & product development activities, platform design, process scale-up & technical transfer and the execution of developmental stability studies.
Responsibilities
- Complete in-vitro transcription, chromatography and filtration purification, LNP encapsulation, and drug product formulation studies.
- Perform in-process testing to understand product yield and recovery and impurity removal.
- Record and summarize data.
- Interact with research and analytical teams.
- Provide support on reviewing documentation in notebooks, present data in group meetings.
- Ensure all experimental procedures and documentation are compliant with highest quality and regulatory standards.
- Partner with diverse team members from several functions, countries and members at multiple levels in the organization.
- Interface with electronic business systems (e.g, ELN).
- Experience with AKTA, Tangential Flow Filtration (TFF), Lipid Nanoparticles (LNP) or mRNA is advantageous.
Qualifications
- Bachelor's degree in related scientific/engineering field, 0-3 years laboratory experience with training in a relevant technical discipline (e.g. molecular and cellular biology, analytical biochemistry, chemical engineering).
- Laboratory experience with training in a relevant technical discipline e.g., molecular and cellular biology, analytical biochemistry.
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
