Upstream Senior Scientist, Process Development

Taylor Strategy Partners

Oklahoma City (OK)

On-site

USD 120,000 - 180,000

Full time

2 days ago
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Job summary

Taylor Strategy Partners in Oklahoma City seeks a Process Development Senior Scientist to drive development, optimization, and scale-up of mammalian upstream bioprocesses for biologics. You will design experiments, analyze data, mentor juniors, and contribute to technology transfer and regulatory documentation in a collaborative biopharma environment.

You will lead cross-functional teams, maintain rigorous data records, and support SH&E/compliance while advancing CMC documentation and process

Qualifications

  • Bachelor's, master's or PhD in Chemical Engineering, Biochemistry, Biotechnology, Biology, or related field.
  • 5–12 years hands-on bioprocessing or biopharmaceutical development 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.
  • Understanding of regulatory standards (cGMP/GLP) is preferred.
  • Strong analytical, problem-solving, and communication skills.

Responsibilities

  • Conduct lab experiments to support mammalian upstream process development.
  • Apply DoE for experimental design and data analysis.
  • Optimize upstream bioprocess parameters for yield and product quality.
  • Support scale-up and tech transfer to manufacturing facilities.
  • Collaborate with analytical, MSAT, manufacturing and quality teams.
  • Prepare buffers, media, and SOP-compliant documentation.

Skills

DoE
Mammalian cell culture
Bioprocess scale-up
Data analysis
Technical documentation

Education

PhD in Biotechnology

Tools

Minitab
DoE software

Job description

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.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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