Upstream Senior Scientist, Process Development

Description

As an upstream Process Development Senior Scientist, you will support the development, optimization, and scale-up of mammalian upstream bioprocesses for the manufacture of biologic drug substances. You will contribute to the design and execution of laboratory experiments, data analysis, and technical documentation.

Key Responsibilities:

• Perform laboratory experiments to support mammalian upstream (cell culture) process development.
• Utilize Design of Experiments (DoE) for data analysis and experimental design.
• Assist in the optimization of upstream bioprocess parameters for yield, purity, and product quality attributes, collaborating with downstream, analytical and formulation teams.
• Support scale-up and technology transfer of processes to manufacturing or pilot facilities based on engineering principles including oxygen transfer.
• Work cross-functionally with analytical development, MSAT, manufacturing and quality teams to drive successful technology transfer.
• Prepare buffers, media, and other solutions according to SOPs and protocols.
• Operate and maintain flask and bioreactor equipment.
• Collect, analyze, and interpret experimental data; maintain accurate lab records and electronic notebooks.
• Present findings in internal and client meetings.
• Author technical reports and regulatory documentation.
• Complete Root Cause Analyses as needed, implementing corrective and preventative actions as needed.
• Mentor junior scientists and research associates in daily activities, data trending and data analysis.
• Follow all safety, quality, and compliance requirements.

Qualifications:

Education:

• Bachelor’s, master’s or PhD degree in Chemical Engineering, Biochemistry, Biotechnology, Biology, or related field.

Experience:

• 5 – 12 years of hands‑on experience in a bioprocessing or biopharmaceutical development environment (academic or industrial); some education qualifications may substitute for some years of experience.
• Experience in a CDMO environment is required.
• Experience with suspension mammalian cell culture and stirred tank bioreactors is required.
• Knowledge of protein purification and analytical techniques is a plus.

Skills and Knowledge:

• Understanding of cGMP, GLP, or other regulatory standards (preferred).
• Strong analytical and problem‑solving skills.
• Good written and verbal communication skills.

Ability to work both independently and in a collaborative team environment.