<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0">
  <channel>
    <title>Wheeler Bio, Inc. Jobs</title>
    <link>https://j.brt.mv/CompanyPortal.do?companyGK=48927&amp;portalGK=39260</link>
    <description><![CDATA[Job Postings available for application.]]></description>
    <language>en-us</language>
    <pubDate>Tue, 09 Jun 2026 19:54:50 EDT</pubDate>
    <lastBuildDate>Tue, 09 Jun 2026 19:54:50 EDT</lastBuildDate>
    <generator>BrightMove ATS</generator>
    <item>
      <title><![CDATA[Senior Program Manager (on-site, based in Oklahoma City) - Oklahoma City, OK]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27772310&amp;companyGK=48927&amp;portalGK=39260</link>
      <guid>fa271279-71f3-48d2-916d-38b65a70c04f</guid>
      <description><![CDATA[Important: This role requires hands-on project leadership experience in regulated pharmaceutical, biotechnology, or aerospace environments, including direct oversight of manufacturing or technical operations. Candidates without this background will not be considered.

Position Overview:
Seeking a driven and resourceful Senior Program Manager to lead complex multi-phase biologics development and manufacturing projects within a CDMO environment. As part of the Commercial team, this position is accountable for the planning and successful delivery of projects in alignment with contracted commitment to clients, regulatory requirements, and Wheeler&rsquo;s revenue goals. Acting as the primary point of contact for clients, the Senior Program Manager will manage timelines, budgets, resources, and cross-functional project teams. This role requires a strategic mindset with exceptional organizational, communication, and critical thinking skills.
 
Key Responsibilities:
Project Leadership & Execution: Lead process development and/or GMP manufacturing projects with end-to-end oversight, managing all project phases to ensure adherence to timelines, budget, quality, and regulatory standards. Develop and maintain Project Plans to manage critical path activities and drive on-time delivery of revenue generating milestones. Effectively handle changes by evaluating and managing change orders, assessing their impact, and ensuring proper documentation, approval, and stakeholder communication.
Client Management: Establish and maintain strong relationships with clients through proactive engagement and clear, concise communication throughout project cycle.
Cross-functional Collaboration: Work closely with process development, manufacturing, quality assurance, regulatory, supply chain, and third-party vendors to coordinate resources and ensure alignment on project deliverables. Partner with the Finance Team to ensure accurate and timely completion of financial transactions.
Risk Management: Proactively identify, assess, and mitigate project risks to ensure project continuity. Develop contingency plans and address potential roadblocks to project success.
Performance Reporting: Generate regular project status reports and documentation to provide stakeholders with visibility into project progress, variances, challenges, and successes.
Continuous Improvement: Identify areas for process improvement and contribute to the development of best practices to enhance organizational efficiency and project outcomes.
 
Qualifications:
Education: Bachelor&rsquo;s degree in Life Sciences, Engineering, or a related field. Advanced degree and/or PMP certification is a plus.
Experience: 3+ years in people leadership and 5+ years in project/program management in regulated pharmaceutical, biotechnology or aerospace environments. Experience in Technical Operations in both product-based and service-based settings is highly desirable.
Technical Know-How: Keen understanding of biologics processes, cGMP manufacturing, supply chain, and regulatory requirements. Expertise in Lean and other process improvement methodologies, with a proven track record of delivering measurable results is a plus.
 
Ideal candidate:
&middot; Proficient in project management tools (e.g., MS Project, Smartsheet) for effective timeline and resource management.
&middot; Master communicator, with ability to navigate stakeholder conflicts and negotiate for best outcomes.
&middot; Critical thinker; able to apply analytical techniques to solve for array of project challenges.
&middot; Solid decision-maker; adopts data-informed approach in guiding Teams methodically to better outcomes.
&middot; Adaptable; able to thrive in a fast-paced, dynamic environment and pivot quickly when faced with changing business priorities and tight deadlines.
&middot; Committed to continuous learning and professional development, with a growth mindset and a passion for excellence.]]></description>
      <pubDate>Wed, 27 May 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Environmental, Health and Safety (EHS) Manager - Oklahoma City, OK]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27770160&amp;companyGK=48927&amp;portalGK=39260</link>
      <guid>d6160d2b-6e97-47da-89db-87c63ef3baa2</guid>
      <description><![CDATA[The EHS Manager is responsible for all Environmental, Health, and Safety programs at Wheeler Bio, ensuring compliance with federal, state, and local regulations (OSHA, EPA, FDA, etc.) while fostering a proactive safety culture and minimizing environmental impact. This role reports directly to the Chief Operating Officer (COO) and closely collaborates with operations, quality, facilities and maintenance across both Development and cGMP manufacturing to embed safety and sustainability into all processes, from design to daily operations. 
Key Responsibilities

Program Development & Implementation: Create and manage EHS policies, procedures, and management systems, including hazard communication (SDS), waste management, and emergency response plans.
Compliance & Auditing: Conduct regular internal audits, inspections, and assessments; manage environmental permits and reporting (e.g., RCRA, SPCC); interface with regulatory agencies.
Risk Management: Perform risk assessments (chemical, biological, physical hazards); investigate incidents/near misses; implement corrective actions and root cause analyses; manage contractor safety.
Training & Culture: Develop and deliver EHS training; promote a strong safety-first culture; coach leaders and employees on best practices.
Data & Reporting: Manage EHS databases (Intelex, etc.); track metrics, analyze trends, and report performance to leadership.
Sustainability: Support and lead initiatives to reduce emissions, manage waste, and improve overall environmental footprint.
Leadership: Serve as a key member of the Extended Leadership Team (ELT), providing technical guidance and ensuring alignment with business objectives. 

Qualifications

Education: Bachelor's degree in Safety Engineering, Environmental Science, Occupational Health, or related field.
Experience: Extensive experience working in a manufacturing environment with a background in chemical, food, or pharmaceutical manufacturing strongly preferred.
Certifications (Preferred): CSP, CIH, CHMM, or relevant HAZWOPER training.
Skills: Strong knowledge of OSHA, EPA, DOT regulations; excellent leadership, communication, and problem-solving skills; ability to build relationships and influence change.]]></description>
      <pubDate>Wed, 27 May 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Process Development Upstream Scientist - Oklahoma City, OK]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27775531&amp;companyGK=48927&amp;portalGK=39260</link>
      <guid>b0b2679e-0a9c-498b-ac98-93338840587b</guid>
      <description><![CDATA[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:
&middot; Perform laboratory experiments to support mammalian upstream (cell culture) process development.
&middot; Assist in the optimization of bioprocess parameters for yield, purity, and product quality.
&middot; Support scale-up and technology transfer of processes to manufacturing or pilot facilities.
&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 and contribute to technical reports and regulatory documentation.
&middot; Complete Root Cause Analyses as needed.
&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; Experience in a CDMO environment is preferred.
&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, 16 Apr 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Senior Director, Process Development - Oklahoma City, OK]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27775153&amp;companyGK=48927&amp;portalGK=39260</link>
      <guid>689a3153-0647-43ca-8a43-60a762e55e9e</guid>
      <description><![CDATA[Position Summary
The Senior Director of Process Development is a senior technical and people leader responsible for the strategic oversight, execution, and continuous improvement of upstream, downstream, and cell line development activities in support of client-sponsored programs and internal technology platforms. This role ensures robust, scalable, and compliant processes that enable successful technology transfer into GMP manufacturing and support regulatory filings across preclinical through commercial stages.
The position serves as a key interface between clients, manufacturing, quality, regulatory, and business development, playing a critical role in maintaining the Wheeler Bio&rsquo;s technical excellence, operational readiness, and client satisfaction.
 
Key Responsibilities
Strategic & Technical Leadership:
&middot;         Define and execute process development strategy aligned with company growth objectives and client portfolio needs
&middot;         Oversee development of scalable, robust, and cost-effective processes for biologics and/or advanced therapeutics (e.g., monoclonal antibodies, multi-specific antibodies, recombinant proteins)
&middot;         Ensure scientific rigor and data integrity across all development activities
&middot;         Stay current with emerging technologies, regulatory guidance, and industry trends to maintain competitive advantage
Program & Client Management:
&middot;         Serve as senior technical lead and escalation point for client programs
&middot;         Provide expert guidance during client engagements, proposal development, and technical due diligence
&middot;         Ensure development timelines, budgets, and deliverables meet client and internal expectations
&middot;         Support technical sections of regulatory submissions (INDs, IMPDs, BLAs, MAAs)
Operational Excellence & Technology Transfer:
&middot;         Drive seamless technology transfer from development to GMP manufacturing
&middot;         Partner closely with Manufacturing, Quality, Supply Chain, and MSAT to ensure process robustness and readiness
&middot;         Establish phase-appropriate and risk-based development approaches and control strategies
People & Organizational Leadership:
&middot;         Lead, mentor, and develop a multidisciplinary team of scientists and managers
&middot;         Build a high-performing, collaborative culture focused on accountability and continuous improvement
&middot;         Support workforce planning, hiring, and talent development initiatives
&middot;         Establish clear performance expectations and career development pathways
Cross-Functional Collaboration:
&middot;         Collaborate with Business Development on proposals, technical assessments, and client onboarding
&middot;         Partner with R&D, MSAT, Manufacturing, Quality, Regulatory Affairs, and Supply Chain to ensure integrated execution
&middot;         Provide executive-level technical input to leadership teams and governance bodies
 
Required Qualifications
Education:
Master&rsquo;s degree or above in Chemical Engineering, Biochemistry, Biotechnology, Chemistry, or related discipline
Experience:
&middot;         12+ years of progressive experience in biopharmaceutical process development, with direct experience in a CDMO regulated manufacturing environment
&middot;         Proven leadership experience managing scientific teams and complex client programs, as well as experience in client-facing leadership roles
&middot;         Demonstrated success developing and scaling processes from early development through commercialization
&middot;         Experience supporting regulatory filings and health authority interactions
Technical Expertise:
&middot;         Deep knowledge of mammalian upstream and/or downstream process development for biologics or advanced therapies
&middot;         Strong understanding of GMP manufacturing, process scale-up, and tech transfer
&middot;         Experience in establishing and maintaining platform processes
&middot;         Familiarity with analytical development, characterization, and control strategies
&middot;         Experience applying QbD, DoE, and risk management tools
Key Competencies:
&middot;         Strategic thinking and decision-making
&middot;         Strong leadership, communication, and influencing skills
&middot;         Client-centric mindset
&middot;         Scientific rigor and problem-solving ability
&middot;         Ability to operate effectively in a fast-paced, deadline-driven environment]]></description>
      <pubDate>Thu, 09 Apr 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Analytical Development Scientist - Oklahoma City, OK]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27767852&amp;companyGK=48927&amp;portalGK=39260</link>
      <guid>459D7246-3B20-73B0-E063-0100007FC485</guid>
      <description><![CDATA[Position Overview: Wheeler Bio is seeking a motivated analytical mind with a passion for problem solving, fast-paced environments, and expertise in protein mass spectrometry to join the analytical team. The Analytical Development Scientist will participate in the development of robust analytical techniques designed for seamless transition to a quality control environment in a manner to emphasize &ldquo;right first time&rdquo; and prolonged success. The position will require broad scientific knowledge of bioanalytical techniques that are used to assess and characterize proteins with a focus on monoclonal antibodies.
Key Responsibilities:

1.    Analytical program management:
&middot;         Manages client analytical programs with a focus on quality and timeline.
&middot;         Leads analytical method development, transfer, and qualification of robust, fit-for-purpose methods to support cGMP testing.
&middot;         Designs, participates in, and reviews required analytical testing according to pre-defined plans and protocols.
&middot;         Writes and reviews analytical plans, protocols, SOPs, and summary reports.
&middot;         Leads transfer of analytical methods to Quality Control.
&middot;         Collaborates with team members and clients to troubleshoot and solve complex problems to meet project needs.
2.    Data analysis and communication:
&middot;         Possesses advanced knowledge of protein biochemistry, analysis, and associated techniques.
&middot;         Independently uses and applies complex instrumentation, computer systems, and software for data acquisition and analysis.
&middot;         Applies knowledge and expertise to critically evaluate data, summarize results, and generate thorough reports.
&middot;         Clearly presents scientific information to senior management, external customers, and/or internal customers 
&middot;         Generates SME content and technical documents (memos, development reports, white papers, presentations etc.).
3.    Continuous improvement:
&middot;         Integrates ongoing quality and operational improvement strategies into workflows.
&middot;         Actively expands scientific expertise to encompass multiple analytical modalities. 
&middot;         Stays abreast of new technologies in the field.
&middot;         Leads development of new analytical methods, processes, or technologies.
4.    Training and personnel management:
&middot;         May oversee team of Analytical Development Associates 
&middot;         Trains and provides guidance to team members and peers
&middot;         As appropriate, leads or participates in training Quality Control, Process Development, and Manufacturing teams performing analytical techniques.
5.    Other duties as assigned.

Qualifications:

Preferred PhD degree (in biochemistry, chemistry, microbiology, or other life-science discipline) with previous industry experience. PhD degree with no prior experience or Master&rsquo;s Degree (in biochemistry, chemistry, microbiology, or other life-science discipline) with at least 2 years of relevant experience will be given consideration.
Advanced knowledge of and experience in protein mass spectrometry (e.g. intact mass, peptide mapping) is strongly preferred.]]></description>
      <pubDate>Mon, 06 Apr 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Manufacturing Supervisor - Oklahoma City, OK]]></title>
      <link>https://j.brt.mv/jb.do?reqGK=27770599&amp;companyGK=48927&amp;portalGK=39260</link>
      <guid>ed3d5bef-91da-46c2-bb6f-e8481821343f</guid>
      <description><![CDATA[Manufacturing Supervisor
POSITION SUMMARY:
We are in search of a proficient and seasoned Manufacturing Supervisor with expertise in GMP (Good Manufacturing Practice) environments, particularly in overseeing cell culture and downstream processing operations. The ideal candidate should possess over 6 years of relevant experience, demonstrating a strong proficiency in cell culture techniques and a track record of ensuring adherence to quality standards. As an integral part of our manufacturing leadership team, you will be instrumental in driving the production of top-tier biopharmaceutical products.
RESPONSIBILITIES:
&middot; Oversee and supervise GMP manufacturing processes for cell culture-based production, ensuring strict compliance with established protocols and regulatory standards.
&middot; Lead routine tasks such as media preparation, cell inoculation, bioreactor operation, and harvest operations, ensuring meticulous execution and adherence to quality parameters.
&middot; Foster collaboration with cross-functional teams, including Quality Control and Quality Assurance, to uphold product quality and regulatory compliance.
&middot; Spearhead troubleshooting efforts and resolution of process deviations, conducting root cause analyses and implementing corrective measures to optimize manufacturing efficiency.
&middot; Maintain comprehensive documentation of all manufacturing activities in accordance with GMP standards, ensuring the accuracy and completeness of batch records and related documentation.
&middot; Play a pivotal role in technology transfer activities, leveraging expertise in cell culture processes to contribute to process enhancement initiatives.
&middot; Facilitate the training and development of junior team members, actively participating in the formulation of standard operating procedures (SOPs) pertaining to cell culture manufacturing.
&middot; Ensure the upkeep of equipment and work areas in accordance with safety protocols and guidelines, fostering a culture of safety and compliance.
PROFESSIONAL SCOPE:
&middot; JOB LEVEL: Assumes responsibility for developing professional expertise, applying company policies and procedures to resolve various issues.
&middot; EXPERIENCE: Typically necessitates a university degree and a minimum of 8 years of relevant experience in a managerial or supervisory capacity.
&middot; COMPLEXITY: Deals with challenges of moderate scope, requiring analysis of diverse factors. Exercises judgment within defined procedures and practices, fostering productive internal and external relationships.
&middot; SUPERVISION: Generally receives general instructions for routine tasks, while detailed instructions are provided for new projects or assignments.
LOCATION:
Wheeler Bio's headquarters are situated in Oklahoma City, OK. The selected individual is expected to operate onsite, necessitating relocation to the Oklahoma City headquarters to oversee this expanding team effectively.
 
CANDIDATE QUALIFICATIONS:
&middot; Bachelor's degree in a pertinent scientific discipline (Biotechnology, Biochemistry, Biology, or a related field) preferred.
&middot; Over 8 years of hands-on experience in GMP manufacturing, with a specialized focus on cell culture processes.
&middot; Profound understanding of bioreactor operations, aseptic techniques, and upstream processing. Experience with tangential flow filtration, ultracentrifugation and bulk fill downstream operations is a plus.
&middot; Hands-on experience with the Thermo Fisher DynaDrive STR system preferred, or comparable STR platforms.
&middot; Familiarity with regulatory requirements governing the production of biopharmaceuticals, including FDA and EMA guidelines.
&middot; Exceptional problem-solving and analytical aptitude, coupled with the capacity to troubleshoot and refine manufacturing processes.
&middot; Strong communication and collaboration skills, enabling effective interaction across departments and fostering a positive team dynamic.
&middot; Detail-oriented with a demonstrated ability to maintain meticulous documentation in compliance with GMP standards.]]></description>
      <pubDate>Mon, 02 Feb 2026 00:00:00 EST</pubDate>
    </item>
  </channel>
</rss>

