Assistant Scientist

Bristol Myers Squibb; Seattle (WA); On-site; USD 52,000 - 59,000; Full time

Job summary

Bristol Myers Squibb is seeking an Assistant Scientist to join the Gene Delivery & Editing Process Development team in Seattle, WA. The role supports upstream and downstream operations in our 250 L pilot lab for production of AAV and Lentiviral vectors used for gene delivery and gene editing of our cell therapy products.

The candidate will help advance scalable, manufacturing-friendly viral vector processes and provide non GMP grade viral vectors for pipeline supporting studies, collaborating

Qualifications

• M.S. or B.S. in Chemical Engineering, Bioengineering, Biochemistry, Molecular Biology, Virology, or related disciplines.
• 0-2 years of industry experience in process development or related work.
• Independently motivated with the ability to multitask and work in teams.
• Ability to communicate clearly and concisely through oral presentation and technical writing.

Responsibilities

• Hands-on experience in upstream (cell culture, bioreactor operation, and transfection conditions) and downstream ( depth filtration, normal flow filtration, tangential flow filtration, chromatography) unit operations for viral vector production.
• Prepare buffers and process solutions for pilot scale productions.
• Contribute to planning and design of experiments, execution and independent analysis of data.
• Maintain proper documentation of process data.

Education

MS or BS in Chemical Engineering, Bioengineering, Biochemistry, Molecular Biology, Virology, or related disciplines

Tools

AKTA

UF/DF

Sterile Filtration

HPLC

ELISA

Job description

• We are seeking an enthusiastic, self-driven individual to join the Gene Delivery & Editing Process Development team. Our team develops process and technology underpinning critical raw materials used in the manufacturing of engineered T cells, including viral vector.
• The primary focus of this Assistant Scientist position will be to support upstream and downstream operations in our 250 L pilot lab for production of AAV and Lentiviral vectors used for gene delivery and gene editing of our cell therapy products. This team member will support current programs, advance process development of scalable, manufacturing-friendly viral vector processes, and provide non GMP grade viral vector for pipeline supporting studies. Join us and be part of a team that values collaboration, personal development, and diversity in pursuit of an inclusive and motivating work environment.

Responsibilities

• Hands-on experience in upstream (cell culture, bioreactor operation, and transfection conditions) and downstream (depth filtration, normal flow filtration, tangential flow filtration, chromatography) unit operations for viral vector production.
• Prepare buffers and process solutions for pilot scale productions.
• Contribute to planning and design of experiments, execution and independent analysis of data.
• Maintain proper documentation of process data.

Basic Qualifications

• M.S. or B.S.in Chemical Engineering, Bioengineering, Biochemistry, Molecular Biology, Virology, or related disciplines.
• 0-2 years of industry experience in process development or related work.
• Independently motivated with the ability to multitask and work in teams.
• Ability to communicate clearly and concisely through oral presentation and technical writing.

Preferred Qualifications

• Demonstrated ability to read and understand scientific literature.
• Experience in mammalian cell culture and aseptic techniques.
• Experience with downstream equipment and techniques (Chromatography/AKTA, UF/DF, Sterile Filtration).
• Familiar with statistical analysis and experimental design.
• Familiar with general analytical assays, such as HPLC and ELISA.

Additional Job Requirements

The starting hourly compensation for this assignment is the following range $38-$42.67/hr). While the final, individual compensation and any available benefits will be determined by your employer of record ASK Staffing, Inc (and not client), factors that will be included in making the final determination may include the characteristics of the assignment, such as demonstrated experience, required skill, and the geographic location where the job is performed. The starting hourly compensation may be subject to change.