Biotech & Pharma STEM OPT Jobs in Oklahoma
Oklahoma's biotech and pharma sector is anchored by employers like OU Health, Integris Health, and life sciences firms in the Oklahoma City and Tulsa metro areas. F-1 STEM OPT authorization applies to qualifying roles in research, bioinformatics, and pharmaceutical sciences, making Oklahoma a viable destination for international graduates seeking hands-on industry experience.
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Get Access To All JobsJob Title: Cell Line Development Scientist
Location: Oklahoma City, OK
Department: Process Development
Job Type: Full-Time
Position Summary:
As a Cell Line Development Scientist, you will support the development, optimization, and creation of mammalian cell lines 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 cell line development and upstream process development.
- Utilize Design of Experiments (DoE) for data analysis and experimental design.
- Coordinate and execute all phases of the CLD process, collaborating with downstream, analytical and formulation teams.
- Work cross-functionally with analytical development, MSAT, manufacturing and quality teams to drive successful technology transfer.
- Translate client amino acid sequences into nucleotide FASTA files to expedite DNA ordering process.
- Prepare buffers, media, and other solutions according to SOPs and protocols.
- Operate and maintain cell line development equipment including electroporation, single cell dispensing, and imaging equipment.
- Program and operate ambr250 microbioreactor system.
- 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:
- 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.
- 4 - 8 years of experience with mammalian stable cell line generation is required.
- Familiarity with transposon-based expression systems is a plus.
- Experience in a CDMO environment is preferred.
- Knowledge of protein purification and analytical techniques is a plus.
Skills and Knowledge:
- Understanding of cGMP, GLP, or other regulatory standards is preferred.
- Strong analytical and problem-solving skills.
- Good written and verbal communication skills.
- Ability to work both independently and in a collaborative team environment.
Physical Requirements:
- Ability to perform lab-based tasks, including standing for long periods, working with various laboratory equipment, and handling biological samples.
- Must be able to lift and carry equipment, reagents, and materials weighing up to 25 pounds.
Working Conditions:
- This position requires flexibility in working hours, including potential shift work, weekends, on-call duties and holidays as necessary.
- Work involves the handling of biological materials.
Job Title: Cell Line Development Scientist
Location: Oklahoma City, OK
Department: Process Development
Job Type: Full-Time
Position Summary:
As a Cell Line Development Scientist, you will support the development, optimization, and creation of mammalian cell lines 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 cell line development and upstream process development.
- Utilize Design of Experiments (DoE) for data analysis and experimental design.
- Coordinate and execute all phases of the CLD process, collaborating with downstream, analytical and formulation teams.
- Work cross-functionally with analytical development, MSAT, manufacturing and quality teams to drive successful technology transfer.
- Translate client amino acid sequences into nucleotide FASTA files to expedite DNA ordering process.
- Prepare buffers, media, and other solutions according to SOPs and protocols.
- Operate and maintain cell line development equipment including electroporation, single cell dispensing, and imaging equipment.
- Program and operate ambr250 microbioreactor system.
- 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:
- 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.
- 4 - 8 years of experience with mammalian stable cell line generation is required.
- Familiarity with transposon-based expression systems is a plus.
- Experience in a CDMO environment is preferred.
- Knowledge of protein purification and analytical techniques is a plus.
Skills and Knowledge:
- Understanding of cGMP, GLP, or other regulatory standards is preferred.
- Strong analytical and problem-solving skills.
- Good written and verbal communication skills.
- Ability to work both independently and in a collaborative team environment.
Physical Requirements:
- Ability to perform lab-based tasks, including standing for long periods, working with various laboratory equipment, and handling biological samples.
- Must be able to lift and carry equipment, reagents, and materials weighing up to 25 pounds.
Working Conditions:
- This position requires flexibility in working hours, including potential shift work, weekends, on-call duties and holidays as necessary.
- Work involves the handling of biological materials.
STEM OPT Biotech & Pharma Job Roles in Oklahoma
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Search Biotech & Pharma Jobs in OklahomaBiotech & Pharma STEM OPT Sponsorship Jobs in Oklahoma: Frequently Asked Questions
Which biotech and pharma companies sponsor F-1 STEM OPT visas in Oklahoma?
Oklahoma employers with documented F-1 STEM OPT hiring in biotech and pharma include research-affiliated hospitals, contract research organizations, and pharmaceutical manufacturers operating in the Oklahoma City and Tulsa corridors. University-affiliated research centers connected to the University of Oklahoma Health Sciences Center and Oklahoma State University also participate in STEM OPT training programs. Employer participation varies by year and role availability, so confirming E-Verify enrollment with each employer is essential before applying.
Which cities in Oklahoma have the most biotech and pharma F-1 STEM OPT sponsorship jobs?
Oklahoma City concentrates the largest share of biotech and pharma STEM OPT opportunities, driven by the Health Sciences Center campus and surrounding medical research institutions. Tulsa offers a secondary cluster through its health system employers and pharmaceutical distribution operations. Stillwater, home to Oklahoma State University's research programs, occasionally generates openings in applied life sciences. Most active STEM OPT postings in Oklahoma are centered within these three metro areas.
What types of biotech and pharma roles typically qualify for F-1 STEM OPT sponsorship in Oklahoma?
Roles that commonly qualify for F-1 STEM OPT in biotech and pharma include research associate positions, bioinformatics analyst roles, quality assurance and regulatory affairs specialists, laboratory technician and scientist titles, and pharmaceutical formulation or process development roles. Qualification depends on the role's Standard Occupational Classification code and whether the employer's offered position aligns with a STEM-designated degree field as recognized by DHS. Reviewing the O*NET classification for a specific role helps confirm eligibility before applying.
How do I find biotech and pharma F-1 STEM OPT sponsorship jobs in Oklahoma?
Migrate Mate filters biotech and pharma job listings by visa type, including F-1 STEM OPT, and by state, so you can surface Oklahoma employers with active sponsorship history rather than guessing from general postings. This is particularly useful in a smaller market like Oklahoma, where STEM OPT-eligible biotech roles are more selective. Pairing Migrate Mate search results with outreach to employer HR contacts about their E-Verify status helps confirm eligibility before investing time in an application.
Are there any state-specific considerations for F-1 STEM OPT sponsorship in Oklahoma's biotech and pharma sector?
Oklahoma's biotech and pharma hiring base is smaller than coastal markets, meaning fewer employers actively maintain E-Verify enrollment, which is a federal requirement for all STEM OPT training plans. Many STEM OPT roles in Oklahoma are attached to academic medical centers or university research grants, which can affect training plan continuity and role duration. International graduates should verify that a prospective employer has a signed training plan process and an HR team experienced with STEM OPT reporting obligations before accepting an offer.