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    <title>Wheeler Bio, Inc. Jobs</title>
    <link>https://ejob.bz/CompanyPortal.do?companyGK=48927&amp;portalGK=39260</link>
    <description><![CDATA[Job Postings available for application.]]></description>
    <language>en-us</language>
    <pubDate>Sat, 31 Oct 2026 06:04:17 EDT</pubDate>
    <lastBuildDate>Sat, 31 Oct 2026 06:04:17 EDT</lastBuildDate>
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      <title><![CDATA[Director of Business Development - Oklahoma City, OK]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27788121&amp;companyGK=48927&amp;portalGK=39260</link>
      <guid>65baa875-111b-4d47-949e-e804f6db8688</guid>
      <description><![CDATA[Director of Business Development
Commercial Team
Reports to: Chief Commercial Officer
Location: Remote
Travel: Approximately 50% travel, including partner visits, Wheeler site visits, internal sales meetings, and representation at industry conferences

ABOUT WHEELER BIO

Wheeler Bio is a High-Science, High-Touch biologics CDMO specializing in antibody-based therapeutics, offering services from discovery through cGMP clinical supply. Our mission is to accelerate the translation of drug discoveries into clinical impact for our customers.
We are proud to be recognized by Newsweek as one of America&rsquo;s Greatest Startup Workplaces 2026. This recognition reflects the strength of our team, our continued growth, and our commitment to our values: Teamwork, Accountability, Integrity, Transparency, and Excellence.

THE ROLE

As Director of Business Development, you will deliver new business for Wheeler Bio. You will be the primary point of contact for our prospects and clients, combining a deep understanding of our services with your industry network to build relationships that fuel our growth today and into the future.

WHAT YOU WILL DO

Build the pipeline
      Identify and qualify new clients using clinical trial databases, financing news, licensing deals, conferences, and your own network.
      Prioritize accounts by program stage, funding, modality fit, and timing of manufacturing decisions.
      Develop and execute territory sales strategies aligned with Wheeler&rsquo;s strategic priorities and marketing opportunities.
Engage clients
      Lead discovery with CMC, technical operations, quality, procurement, and executive stakeholders to understand client program needs and decision criteria.
      Tailor your message to each audience: technical proof for CMC leaders, commercial clarity and risk terms for procurement.
      Partner with commercial team members and technical subject matter experts on targeting, technical deep dives, site visits, and audits.
Close the deal
      Orchestrate and own client proposals in collaboration with Business Operations to deliver accurate scope, pricing, and timelines.
      Negotiate commercial terms, including MSAs, SOWs, NDAs, MTAs, capacity reservations, and supply agreements, with support from Legal and the CCO.
      Close new business to achieve or exceed annual bookings targets.
Advancing Client Relationships
      Guide new clients from program award through onboarding and handover to the Operations project management teams.
      Introduce new and existing clients to additional Wheeler services.
      Track and report key sales metrics, adjusting strategy based on the data.
      Evangelize Wheeler Bio&rsquo;s capabilities at tradeshows, roadshows, conferences, and summits.

WHAT YOU BRING

      Bachelor&rsquo;s degree, preferably in Life Sciences or Engineering. A master&rsquo;s degree or MBA is a plus.
      5+ years of CDMO sales experience in large molecule drug substance or drug product.
      A proven track record of achieving year over year territory growth goals driven by new account and new program acquisition.
      An established network of partner relationships across the industry.
      Strong understanding of clinical development phases, large molecule process development and manufacturing (including late phase requirements), and GMP and regulatory requirements.
      Advanced CRM proficiency (Salesforce) combined with modern digital content strategies to build targeted outbound campaigns, nurture partner relationships, and scale the sales pipeline.

HOW YOU WORK

      You build high-trust, consultative relationships with biotech executives, navigating complex program challenges and aligning technical realities with strict clinical timelines.
      You keep stakeholders engaged across 12+ month CDMO sales cycles, adapting your strategy to client feedback, funding landscapes, and shifting market conditions.
      You use competitive landscape and market trend analysis to shape territory strategy and position Wheeler&rsquo;s high-science CDMO services for multi-year value for Wheeler and its partners.
      You serve as the bridge between clients and internal leadership, advocating for the resources, pricing, and custom program scopes that win business.
      You drive remote territory growth while bringing together Business Operations, Finance, Legal, and technical SMEs to close complex deals.
      You achieve or exceed bookings and revenue targets through disciplined pipeline management, continuous refinement of your sales tactics, and an aggressive focus on measurable growth.
 
COMPENSATION & BENEFITS
At Wheeler Bio, we reward our team members for their vital contributions to our mission. We offer a highly competitive compensation package designed to recognize your expertise and drive, alongside a comprehensive benefits program that supports your health, well-being, and financial future. Join us and thrive both personally and professionally as we scale new heights together!

EQUAL OPPORTUNITY

Wheeler Bio is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected by law.]]></description>
      <pubDate>Thu, 29 Oct 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Manufacturing Sciences and Technologies (MSAT) Engineer II - Oklahoma City, OK]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27787360&amp;companyGK=48927&amp;portalGK=39260</link>
      <guid>4ec0ae57-8826-4a4d-9374-77c6598a5958</guid>
      <description><![CDATA[The main responsibility of the MSAT Engineer II is to support the manufacturing team, fellow MSAT Scientists, and Process Engineers as a technical advisor and through the development, implementation and continual improvement of technical transfers of processes to manufacturing scale. The MSAT Engineer II will have a thorough understanding of adaptation of mammalian upstream and downstream processes demonstrated at the R&D/Lab scale to the suitable manufacturing scale, authoring bill of materials, process flow diagrams, risk assessments, facility fit assessments of equipment capabilities, validation protocols (as needed for manufacturing execution) and investigations, and reviewing process descriptions or other internal or external process documents. Collaborates with Facilities and Engineering to determine equipment requirements and to support equipment troubleshooting.
 
Responsibilities 
&middot;         Follow established policies, procedures, and strategies that are consistent with cGMP regulations for early and late-phase programs.
&middot;         Adhere to Quality standards and regulatory requirements.
&middot;         Possess proficiency in understanding the concepts and scale-up requirements for mammalian cell culture and downstream purification, including TFF, chromatography and viral clearance.
&middot;         Advise internal and external development groups on manufacturing scale feasibility throughout process lifetime.
&middot;         Assist in the generation of process and facility fit assessments by providing technical expertise on equipment capabilities
&middot;         Author and review Bill of Materials for internal or external processes and assist in material readiness for manufacturing activities.
&middot;         Author, review, and approve documents for technology transfer as needed, including batch records, protocols and Summary/Engineering run reports.
&middot;         Provide technical expertise for equipment readiness and operations for internally or externally developed processes.
&middot;         Participate in and author, review or approve documents for Failure Mode and Effects Analysis (FMEA) for processes as needed.
&middot;         Provide support to manufacturing or MSAT personnel during active manufacturing campaigns by performing and analyzing data trending and troubleshooting issues with the ability to interpret process trends and data. 
&middot;         Collaborate with the Quality Assurance department as needed to provide input on materials, deviations, impact assessments, risk assessments, change control, CAPAs, and process validation if applicable.
&middot;         Coordinate with other departments to maintain process timelines.
&middot;         Lead and participate in troubleshooting to improve operations.
&middot;         Other duties as assigned.
 
Knowledge / Skills / Experience Requirements
&middot;         PhD or MS in engineering or a relevant life-science field with a minimum of 3 years industry experience in GMP production.
&middot;         BS in engineering or relevant life-science related field with a minimum of 5 years industry experience in GMP Production.
&middot;         Experience in technical transfer and scale-up of biologics drug substance required; experience with single-use technologies preferred.
&middot;         Knowledge of FDA, ICH, EMA, JP, and other regulatory guidance on CGMP manufacturing.
&middot;         Strong written, oral, and presentation skills.
&middot;         Strong attention to detail with a focus on product quality requirements.
&middot;         Proven track record of complex problem solving with use of ingenuity and creativity.
&middot;         Strong interpersonal, collaboration, and leadership skills.
&middot;         Ability to work flexible hours and inconsistent schedules as necessary to meet production demands and timelines.]]></description>
      <pubDate>Mon, 19 Oct 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Cell Line Development Scientist - Oklahoma City, OK]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27784634&amp;companyGK=48927&amp;portalGK=39260</link>
      <guid>31c83443-f647-4de9-aabe-40ab2cb2eb42</guid>
      <description><![CDATA[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:
&middot;                     Perform laboratory experiments to support mammalian cell line development and upstream process development.
&middot;                     Utilize Design of Experiments (DoE) for data analysis and experimental design.
&middot;                     Coordinate and execute all phases of the CLD process, collaborating with downstream, analytical and formulation teams.
&middot;                     Work cross-functionally with analytical development, MSAT, manufacturing and quality teams to drive successful technology transfer.
&middot;                     Translate client amino acid sequences into nucleotide FASTA files to expedite DNA ordering process.
&middot;                     Prepare buffers, media, and other solutions according to SOPs and protocols.
&middot;                     Operate and maintain cell line development equipment including electroporation, single cell dispensing, and imaging equipment.
&middot;                     Program and operate ambr250 microbioreactor system.
&middot;                     Collect, analyze, and interpret experimental data; maintain accurate lab records and electronic notebooks.
&middot;                     Present findings in internal and client meetings.
&middot;                     Author technical reports and regulatory documentation.
&middot;                     Complete Root Cause Analyses as needed, implementing corrective and preventative actions as needed.
&middot;                     Mentor junior scientists and research associates in daily activities, data trending and data analysis.
&middot;                     Follow all safety, quality, and compliance requirements.
 
 
 
Qualifications:
Education:
&middot;                     Bachelor's, Master's or PhD degree in Chemical Engineering, Biochemistry, Biotechnology, Biology, or related field.
Experience:
&middot;                     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.
&middot;                     4 - 8 years of experience with mammalian stable cell line generation is required.
&middot;                     Familiarity with transposon-based expression systems is a plus.
&middot;                     Experience in a CDMO environment is preferred.
&middot;                     Knowledge of protein purification and analytical techniques is a plus.
Skills and Knowledge:
&middot;                     Understanding of cGMP, GLP, or other regulatory standards is preferred.
&middot;                     Strong analytical and problem-solving skills.
&middot;                     Good written and verbal communication skills.
&middot;                     Ability to work both independently and in a collaborative team environment.
 
Physical Requirements:
&middot;         Ability to perform lab-based tasks, including standing for long periods, working with various laboratory equipment, and handling biological samples.
&middot;         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.]]></description>
      <pubDate>Fri, 04 Sep 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Upstream Senior Scientist, Process Development - Oklahoma City, OK]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27779310&amp;companyGK=48927&amp;portalGK=39260</link>
      <guid>603f8c02-7c58-4e0b-b355-7eeba84bf749</guid>
      <description><![CDATA[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:
&middot;                     Perform laboratory experiments to support mammalian upstream (cell culture) process development.
&middot;                     Utilize Design of Experiments (DoE) for data analysis and experimental design.
&middot;                     Assist in the optimization of upstream bioprocess parameters for yield, purity, and product quality attributes, collaborating with downstream, analytical and formulation teams.
&middot;                     Support scale-up and technology transfer of processes to manufacturing or pilot facilities based on engineering principles including oxygen transfer.
&middot;                     Work cross-functionally with analytical development, MSAT, manufacturing and quality teams to drive successful technology transfer.
&middot;                     Prepare buffers, media, and other solutions according to SOPs and protocols.
&middot;                     Operate and maintain flask and bioreactor equipment.
&middot;                     Collect, analyze, and interpret experimental data; maintain accurate lab records and electronic notebooks.
&middot;                     Present findings in internal and client meetings.
&middot;                     Author technical reports and regulatory documentation.
&middot;                     Complete Root Cause Analyses as needed, implementing corrective and preventative actions as needed.
&middot;                     Mentor junior scientists and research associates in daily activities, data trending and data analysis.
&middot;                     Follow all safety, quality, and compliance requirements.
 
Qualifications:
Education:
&middot;                     Bachelor's, master's or PhD degree in Chemical Engineering, Biochemistry, Biotechnology, Biology, or related field.
Experience:
&middot;                     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.
&middot;                     Experience in a CDMO environment is required.
&middot;                     Experience with suspension mammalian cell culture and stirred tank bioreactors is required.
&middot;                     Knowledge of protein purification and analytical techniques is a plus.
Skills and Knowledge:
&middot;                     Understanding of cGMP, GLP, or other regulatory standards (preferred).
&middot;                     Strong analytical and problem-solving skills.
&middot;                     Good written and verbal communication skills.
&middot;                     Ability to work both independently and in a collaborative team environment.]]></description>
      <pubDate>Thu, 11 Jun 2026 00:00:00 EDT</pubDate>
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