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Biotech Process Development Jobs in Oklahoma (NOW HIRING)

Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Supporting the development and testing of DeltaV automation software * Troubleshooting system and ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

Supporting the development and testing of DeltaV automation software * Troubleshooting system and ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

Supporting the development and testing of DeltaV automation software * Troubleshooting system and ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

Supporting the development and testing of DeltaV automation software * Troubleshooting system and ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

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Biotech Process Development information

See Oklahoma salary details

$17

$28

$39

How much do biotech process development jobs pay per hour?

As of May 30, 2026, the average hourly pay for biotech process development in Oklahoma is $28.80, according to ZipRecruiter salary data. Most workers in this role earn between $25.10 and $31.78 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Biotech Process Development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What are popular job titles related to Biotech Process Development jobs in Oklahoma? For Biotech Process Development jobs in Oklahoma, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Oklahoma look for? The top searched job categories for Biotech Process Development jobs in Oklahoma are:
What cities in Oklahoma are hiring for Biotech Process Development jobs? Cities in Oklahoma with the most Biotech Process Development job openings:
Process Development Upstream Scientist

Process Development Upstream Scientist

Wheeler Bio, Inc.

Oklahoma City, OK • On-site

Full-time

Posted 13 days ago


Job description

Position Summary:

As a Process Development 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.

· Assist in the optimization of bioprocess parameters for yield, purity, and product quality.

· Support scale-up and technology transfer of processes to manufacturing or pilot facilities.

· 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 and contribute to technical reports and regulatory documentation.

· Complete Root Cause Analyses as needed.

· 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:

· 4-8 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 preferred.

· 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.