Postdoctoral scholar jobs in Houston, TX - 171 jobs

Kindbody is a leading fertility clinic network and family-building benefits provider, delivering comprehensive reproductive care across the U.S. Our mission is to make fertility and family-building more accessible and affordable while ensuring superior health outcomes through clinical excellence and a seamless patient experience. About the Role As a Senior Embryologist at Kindbody, you will be working in a fast-paced, rapidly growing environment where you will be relied on for your expertise, professionalism, and collaboration. We consider our Senior Embryologists to be someone who is fully trained & signed off in all aspects of Embryology (basic + micro manipulation) for 6+ years. Responsibilities Perform Chemistry Laboratory and Andrology Laboratory Procedures as needed. Perform assisted reproductive technology methods, including but not limited to semen preparation, oocyte identification, conventional IVF, ICSI, embryo culture and grading, laser-assisted hatching, trophectoderm biopsy, sperm, oocyte, and embryo cryopreservation (vitrification). Maintain accurate laboratory records Perform quality control procedures and monitor KPIs Participate in the laboratory's quality management program Coordinate with reproductive endocrinologists and OB/GYNs to assist their patients with reproductive health issues and clinical research. Communicate with patients on outcomes, lab procedures, and general patient lab-related questions as needed Ensure all patient information is documented appropriately in our EMR according to our procedures Works independently to ensure the program goals are achieved Support and promote excellence in customer service Provide feedback to HQ on process improvement and job specifications to help gain efficiencies in the day-to-day Is willing to travel to other Kindbody locations to perform patient testing, train or support staff. Is willing to collaboratively support the Kindbody team remotely or locally with their expertise. Assist with projects, tasks, and team support as needed. Who You Are 6+ years experience in clinical embryology {3-4 of which are micromanipulation} TS (ABB) certified or eligible Able to work independently with minimal supervision Proficiency in all IVF laboratory methods, including micromanipulation techniques and vitrification Detail-oriented, meticulous record-keeping Strong communication skills & a team player Willingness to be flexible Familiarity with all state and local regulations, including tissue bank licensing Experienced in EMR and G-Suite

Primary purpose is to research new bankruptcy cases. Once a case is found to have delinquent taxes for one of the Firms clients, you will prepare Proofs of Claim and Notices of Appearance. In addition, you will key in this data into BankTool and code account(s) in Tax Tool. Describe this positions Essential Functions: (Tasks, duties & responsibilities of the job. Outline the core responsibilities of the position. Highlight the day-to-day activities of the position). 1. Research: Research new bankruptcy cases filed for individuals under Chapter 13 and Chapter 7 for any taxes owed to clients. 2. Research: Review all cases included in each PACER case filing report provided by various offices for any taxes owed to clients. 3. Research: Research and review Petitions, Schedules, Statement of Financial Affairs, and all amendments, for any taxes owed to clients. 4. Research: Review snail mail and emails daily to research and review for additional bankruptcy cases that need claims prepared or amended. 5. Administrative: Prepare Proofs of Claim and Notices of Appearance in a timely manner. 6. Administrative: Input new case info into Bank Tool. 7. Administrative: Prepares Proofs of Claim for Court Costs & Fees. 8. Administrative: Contacts various firm staff and jurisdictions for additional tax information. 9. Administrative: Prepare amendments to proofs of claim to add, remove, or update tax claims, including updating Bank Tool with the changes. 10. Communicate and coordinate with consumer case paralegals to shift priority on cases needing immediate attention. 11. Complete recurring special projects to amend claims, updating estimated amounts to actual amounts as needed. 12. Research: Review foreclosure lists for any active bankruptcies. 13. Occasionally may perform other duties within the scope of the job Describe the Physical Demands & Work Environment 1. Physical demands are sitting at desk and lifting 5lbs or less from time to time. 2. Work environment is very open, friendly and courteous. 3. Employee is required to sit, walk, and use hands and fingers to operate office equipment. 4. Visual abilities include viewing computer screens and the ability to adjust focus. Package Details

Researcher Firm SummaryWhite & Case is an elite global law firm serving leading companies, financial institutions and governments worldwide. Our long history as an international firm means we are perfectly placed to help our clients resolve their most complex legal challenges wherever they may be. With lawyers operating from more than 40 locations, working in virtually every country of the world, we have invested heavily in building a high-quality full-service practice competing at the top of the market. We are distinguished by our on-the-ground presence in the world's key financial markets and our strength in handling complex cross-border work. It's not just about our global network of offices; it's the global interconnectedness of the Firm that our people, and our clients, value most. We work well together across geographic and practice boundaries. It's one of the reasons we attract and retain cross-border work. Our lawyers are globally minded, enterprising, collaborative and committed to excellence. Our people represent 90 nationalities and speak 80 languages. Position SummaryThe Researcher will be part of the global Practice Solutions team and will conduct substantive research across a range of practice areas and deliver insights for client work and business development efforts. They will also coordinate and conduct formal and informal attorney training on research tools and methodology, lead a variety of short- and long-term research projects, and participate in broader department strategic initiatives. As part of a global research team, the Researcher will collaborate with colleagues to provide research across White & Case offices. Our TeamThe global Research & Market Intelligence team delivers research to support client work and matters and provides actionable competitive intelligence to support business and client development efforts. The team also works to ensure that we have the optimal selection of research tools and expertise to help build and sustain the Firm's practices. Our goal is to provide research support to benefit unique and complex client and practice needs across the globe. Duties and Accountabilities1Performs substantive research using online and print information to support local and global practices. Provides competitive intelligence and background research on current or potential clients and markets in support of business and client development efforts. Proactively and independently assesses research requests to ensure that the research meets stated and anticipated needs. Educates attorneys and staff on research resources and methodology, and ensures effective promotion of research services to attorneys and legal staff. Uses current awareness tools to create newsletters and alerts for ongoing monitoring of clients, industries and events. Participates in evaluating and developing the research collection and piloting new services, including generative AI tools and other AI technologies. Ensures continuing professional development and keeps abreast of the legal industry. Provides cross-training and mentoring to colleagues in other offices. Incorporates Generative AI into daily work as appropriate and trains or advises lawyers and others on Generative AI services. QualificationsFive or more years of broad research experience required, plus Master's degree in library or information science, law degree, or other relevant advanced degree strongly preferred, or an equivalent combination of relevant education and experience. Successful candidates will have experience with the energy industry to support our global Energy practice and assist with complex research queries from our Houston-based attorneys. Strong preference will be given to candidates with Spanish-language skills. Essential Job RequirementsEvidence of strong research and problem-solving skills, including the ability to absorb large amounts of information and synthesize into actionable intelligence. Knowledge of key legal and corporate-focused databases and tools is preferred, including Lexis+, Westlaw Edge, Bloomberg Law, Lex Machina, Intelligize, Capital IQ, MergerMarket, among others. Strong data literacy skills and experience with data manipulation preferred. Resourceful, proactive, with a demonstrated ability to prioritize effectively and meet tight internal and external deadlines. Evidence of a strong client service focus, superior written and oral communication skills, and the ability to build productive relationships with internal and external clients,Ability to apply strong, independent judgment at all times, and to see the big picture. Ability to handle sensitive matters and maintain confidentiality. Availability to work outside regular work hours as needed to meet firm business needs. Equal OpportunitiesWhite & Case is an Equal Employment Opportunity (EEO) employer and is committed to creating a fair workplace. It is our Firm's policy to recruit, employ, train, compensate and promote without regard to race, color, religion, creed, national origin, age, gender, sexual orientation, marital status, military or veteran status, disability, genetic information, or any other category protected by applicable law. Applicants who are interested in applying for a position and require an accommodation during the process should contact talent. acquisition@whitecase. com. Benefits at White & CaseWhite & Case LLP offers a comprehensive suite of benefit programs to all eligible employees, including medical, dental, and vision insurance, life and disability coverage, 401(k) retirement savings, vacation time, and leave programs (including parental leave). Exempt roles are also performance bonus eligible. Note to Recruitment AgenciesOur Internal Recruitment team are responsible for all end-to-end lateral recruitment process. All agencies must sign White & Case terms of business which are often specific. Candidates submitted by an agency without terms of business agreed with the appropriate office, and/or outside of our online application tracking system, will not be considered a formal introduction. Any applications and CVs sent directly to White & Case Partners and employees will not be accepted as formal introductions. If you have any questions, please contact the Americas Lateral Recruitment team. Location & ReportingThis role is based in Houston, TX. Ideal work schedule is 10 a. m. - 6:30 p. m. Central. This role reports to the Manager, Research & Market Intelligence for the Americas. The firm may modify and amend this job description at any time in its sole discretion. Nothing herein creates a contract of employment or modifies the at-will nature of employment Primary Location: United States-Houston Expected Workplace: Onsite Job Posting: Dec 15, 2025, 6:40:22 PM Refer a friend for this job Tell us about a friend who might be interested in this job. All privacy rights will be protected. Refer a friend

About the Harris County Public Defender's Office The Harris County Public Defender's Office (HCPDO), established in 2010, is a dynamic public defense office that is becoming one of the largest in the country, with over 300 employees, including more than 200 attorneys. We are a client-centered, holistic public defense office dedicated to fighting for fairness in one of the nation's largest and most complex criminal legal systems. Our interdisciplinary teams, which include attorneys, social workers, investigators, mitigation specialists, and other professionals, provide a wrap-around advocacy that addresses both the case and the person. HCPDO's work goes beyond individual representation. We are committed to systemic change and community empowerment, advancing justice through participatory defense, immigration advisal, and support for the private bar. Our core values: client-centered representation, professionalism in advocacy, teamwork, collaboration, community empowerment, and systemic change; guide everything we do. What We Offer * Working at HCPDO means joining a collaborative, mission-driven community of advocates who believe in excellence and support one another at every step. * Extensive Training & Development - Frequent in-house training and CLE's, case reviews, brainstorming sessions, and trial skills workshops (including voir dire and advocacy practice). Attorneys are also supported in attending statewide CLEs and training. * Mentorship & Built-In Support - Our culture is deeply collaborative: no attorney goes to trial alone. Every trial has a required second chair, ensuring built-in guidance and teamwork. * Courtroom Experience - Attorneys gain meaningful courtroom exposure early in their careers while benefiting from mentoring and structured training. * Work-Life Balance - Caseloads are capped, ensuring sustainability and allowing attorneys to provide high-level representation. * Holistic, Client-Centered Advocacy - Attorneys work alongside investigators, social workers, mitigation specialists, and other professionals to provide comprehensive representation. * Comprehensive Benefits - As Harris County employees, attorneys receive full benefits, including health, dental, vision, retirement, and paid leave. Position Overview The HCPDO seeks third-year law students (3Ls) graduating in Spring 2026, as well as recent law school graduates, to join our team as Post-Bar Fellows. Applicants must have either completed the Texas Bar Exam or be registered to take it and awaiting results when the fellowship begins. This fellowship offers a unique and immersive opportunity to gain hands-on experience in indigent criminal defense. Fellows begin with HCPDO's 10-week Fellowship Training Bootcamp, a program that combines onboarding, substantive training, courtroom shadowing, and supervised client advocacy. Through this intensive experience, fellows work alongside experienced public defenders and play an active role in all stages of representation - from case investigation and legal research to client advocacy and trial preparation. Duties and Responsibilities * Conduct legal research and draft memoranda, motions, and other pleadings under attorney supervision. * Assist attorneys in reviewing discovery, investigating cases, and formulating defense strategies. * Participate in client interviews, jail visits, and witness preparation. * Organize case files and assist in trial preparation, including reviewing evidence and preparing exhibits. * Observe and participate in court proceedings, including pre-trial hearings, motions, and plea negotiations. * Collaborate with attorneys, investigators, and social workers to ensure holistic representation of clients. * Uphold the mission and values of the HCPDO by ensuring zealous advocacy and ethical representation. Harris County is an Equal Opportunity Employer ************************************************************************* If you need special services or accommodations, please call ************** or email ***************************. This position is subject to a criminal history check. Only relevant convictions will be considered and, even when considered, may not automatically disqualify the candidate. Requirements Required Supporting Documents: * Resume * Cover Letter * Must explain why you want to do this work * Applications without a cover letter will not be considered * Include lived, educational, or professional experiences that have prepared you for the role * Add any other information for the hiring committee to consider. * Law school transcript (an unofficial transcript is acceptable). * Contact information for at least two professional references. Education and Experience: * J.D. from an accredited law school by the fellowship start date. * Eligible applicants include recent graduates, individuals finishing judicial clerkships or fellowships who plan to transition into public defense, and those eager to start a career in public defense immediately after graduation. * Applicants must be: * 3L student or recent law school graduate preparing to take the July 2026 Texas Bar Exam OR * A recent law school graduate who is already licensed in Texas NOTE: Qualifying education, experience, knowledge, and skills must be documented on your job application. You may attach a resume to the application as supporting documentation but ONLY information stated on the application will be used for consideration. "See Resume" will not be accepted for qualifications. Preferences The ideal candidate will have the following skills and abilities: * Strong research, analytical, and written communication skills. * Ability to thrive in a fast-paced environment. * Strong organizational and time management skills. * Demonstrated commitment to public service, indigent criminal defense, and social justice. General Information Deadlines & Review * Early Decision Deadline: November 30 * Applications will be reviewed, and interviews will be scheduled on a rolling basis. Position Type and Typical Hours of Work: * Seasonal Full-time * Monday - Friday | 8:00 AM - 5:00 PM Desired Start Date: * 8/17/2026 | Approximately 3 months, beginning after completion of the Texas Bar Exam. * This fellowship is intended to lead directly to employment with HCPDO (subject to performance and office needs). Employment may be contingent on passing a drug screen and meeting other standards. Due to a high volume of applications positions may close prior to the advertised closing date or at the discretion of the Hiring Department. Applications will be reviewed on a rolling basis. For questions or concerns regarding the application, please contact: ************************ HARRIS COUNTY EMPLOYEE BENEFITS Harris County offers a highly competitive benefits program, featuring a comprehensive group health plan and defined benefit retirement plan. The following benefits are offered only to Harris County employees in regular (full-time) positions: Health & Wellness Benefits * Medical Coverage * Dental Coverage * Vision Coverage * Wellness Plan * Life Insurance * Long-Term Disability (LTD) Insurance * Employee Assistance Program (EAP) * Healthcare Flexible Spending Account * Dependent Care Flexible Spending Account Paid Time Off (PTO) * Ten (10) days of vacation leave per year (accrual rate increases after 5 years of service) * Eleven (11) County-observed holidays * One (1) floating holiday per year * Paid Parental Leave* * Sick Leave Retirement Savings Benefit * 457 Deferred Compensation Plan The following benefits are available to Harris County employees in full-time and select part-time positions: * Professional learning & development opportunities * Retirement pension (TCDRS defined benefit plan) * Flexible work schedule* * METRO RideSponsor Program* * Participation may vary by County department. The employee benefits plans of Harris County are extended to all eligible participants across various departments with the exception of the Harris County Community Supervision and Corrections Department, for which the cited Health & Wellness Benefits are administered through the State of Texas. In accordance with the Harris County Personnel Regulations, group health and related benefits are subject to amendment or discontinuance at any time. Harris County Commissioners Court reserves the right to make benefit modifications on the County's behalf as needed. For plan details, visit the Harris County Benefits & Wellness website: ********************** 01 Have you completed or will you have completed a Juris Doctorate degree by the start of the fellowship? * Yes * No 02 Please describe your educational background including level of education completed, area of study and completed major and minor programs. 03 Are you currently licensed to practice law with the State Bar of Texas? * Yes * No 04 Will you be sitting for the Texas Bar Exam and awaiting results at the time the fellowship begins? * Yes * No 05 Interested candidates must submit the following materials: 1 . Resume 2. Cover letter (review job posting for guidelines) 3. Law school transcript 4. At least two (2) professional references and their contact information Did you attach all required documents to your application? * Yes Required Question Employer Harris County Address 1111 Fannin St Ste. 600 Houston, Texas, 77002 Phone ************ Website *****************************************************

JobID: 210672538 JobSchedule: Full time JobShift: Day Base Pay/Salary: Jersey City,NJ $152,000.00-$260,000.00; New York,NY $152,000.00-$260,000.00; Chicago,IL $133,000.00-$225,000.00; Brooklyn,NY $152,000.00-$260,000.00 As an Vulnerability Researcher - Assessments & Exercises at JPMorgan Chase in the Cybersecurity Technology & Controls line of business, you will contribute significantly to enhancing the firm's cybersecurity or resiliency posture by using industry-standard assessment methodologies and techniques to proactively identify risks and vulnerabilities in people, processes, and technology. Design and deploy risk-driven tests and simulations (or manage a highly-skilled team that does) and inform analysis to clearly outline root-causes. In this role, you will evaluate preventative controls, incident response processes, and detection capabilities, and advise cross-functional teams on security strategy and risk management. We are seeking a dedicated vulnerability researcher to engage in advanced vulnerability analysis and research, addressing the complex demands of our mission. In this role, you will work closely with fellow researchers and defense teams to identify vulnerabilities and develop cutting-edge solutions. The ideal candidate will be self-motivated, possess extensive technical curiosity, and have a strong background in reverse engineering. You will thrive in a collaborative environment, working on challenging targets to enhance our security posture. Job responsibilities * Design and execute testing and simulations - such as penetration tests, technical controls assessments, cyber exercises, or resiliency simulations, and contribute to the development and refinement of assessment methodologies, tools, and frameworks to ensure alignment with the firm's strategy and compliance with regulatory requirements * Evaluate controls for effectiveness and impact on operational risk, as well as opportunities to automate control evaluation * Collaborate closely with cross-functional teams to develop comprehensive assessment reports - including detailed findings, risk assessments, and remediation recommendations - making data-driven decisions that encourage continuous improvement * Utilize threat intelligence and security research to stay informed about emerging threats, vulnerabilities, industry best practices, and regulations. Apply this knowledge to enhance the firm's assessment strategy and risk management. Engage with peers and industry groups that share threat intelligence analytics * Conduct in-depth vulnerability research and exploit development across a broad range of software on modern operating systems, edge devices, on premise, and open-source software. * Reverse engineer binaries using tools such as IDA Pro, Ghidra, or Binary Ninja to identify novel attack surfaces and develop proof-of-concept exploits. * Use common VR toolsets such as Fuzzers, disassemblers, debuggers, and code browsers for static and dynamic analysis. * N-Day vulnerability analysis, patch diffing, and zero-day vulnerability research. * Collaborate with other teams to share findings, support vulnerability triage, patch prioritization, and IOCs sharing, supporting the firm's mission requirements. * Document research findings, proof-of-concepts, and technical workflows. Required qualifications, capabilities, and skills * Obtain 5+ years of experience in cybersecurity or resiliency, with demonstrated exceptional organizational skills to plan, design, and coordinate the development of offensive security testing, assessments, or simulation exercises * Track record of discovered vulnerabilities (CVEs) in high-profile targets in at least one of the following environments: operating systems, mobile devices, web applications, browsers. * Proven hands-on experience in vulnerability research and PoC/exploit development, reporting, and mitigating security vulnerabilities in open-source projects. * Expertise in advanced analysis frameworks leveraging symbolic execution techniques and dynamic binary instrumentation to uncover, triage, and exploit complex software vulnerabilities. * Hands-on proficiency exploiting complex vulnerability classes - including user-after-free, double free, type confusion - and applying advanced exploitation techniques such as heap spraying and controlled memory corruption to achieve reliable code execution. * Strong understanding of at least two operating systems internals throughout user mode and kernel mode (Microsoft Windows, GNU/Linux, Android, MacOS, or iOS). * Experience auditing large C/C++, Java, and .Net codebases combining automated static analyzers with manual review to trace data and control flow, uncover memory-safety, injection, and deserialization vulnerabilities and produce proof-of-concept code. * Extensive reverse engineering expertise on x86/x64 and ARM/ARM64 binaries, employing IDA Pro, Ghidra, Binary Ninja, WinDbg, GDB, and RR for deep static/dynamic analysis and root cause vulnerability discovery. * Knowledge of US financial services sector cybersecurity or resiliency organization practices, operations risk management processes, principles, regulations, threats, risks, and incident response methodologies * Ability to identify systemic security or resiliency issues as they relate to threats, vulnerabilities, or risks, with a focus on recommendations for enhancements or remediation, and proficiency in multiple security assessment methodologies (e.g., Open Worldwide Application Security Project (OWASP) Top Ten, National Institute of Standards and Technology (NIST) Cybersecurity Framework), offensive testing tools, or resiliency testing equivalents * Excellent communication, collaboration, and report writing skills, with the ability to influence and engage stakeholders across various functions and levels Preferred qualifications, capabilities, and skills * Bachelor's degree in computer science, or PhD in a related technical field, or an equivalent combination of education and/or experience in a related field. * 5+ years of experience in exploit research and development. * Experience using Fuzzing tools such as LibFuzzer, LibAFL, AFL++, OSS-Fuzz, Syzkaller and program analysis tools such as LLVM, Angr, KLEE, Intel Pin, DynamoRIO, and Frida. * Experience emulating embedded platforms for live debugging. * Kernel and low-level OS development. * Deep Linux internals knowledge (SELinux, AppArmor, Seccomp, eBPF, containers, VMs). * Deep Windows internals knowledge (KASLR, DSE, SSDT, IDT, SMEP, SMAP, PXN, KPP, KDP, VBS, HVCI, KMCI, UMCI).

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Lonza is currently seeking an experienced Scientist II, BioAssay Services to join their team in Houston, TX. POSITION: Scientist II, BioAssay Services JOB LOCATION: 14905 Kirby Dr, Houston, TX 77047 DUTIES: Design analytical methodology for the characterization of Cell and Gene Therapies. Execute analytical testing to characterize Cell and Gene Therapy drug products/substances. Validate analytical methodology for the characterization and release of Cell and Gene Therapies. Transfer analytical methodologies to the quality control laboratory and train quality control analysts. Lead client discussion and drive project direction. Manage project timelines and delivery. Lead a project team in a matrix organization to deliver projects on-time and in-full. Develop junior scientists analytical capability through direct on-the-job training and mentorship. Present and explain complex scientific concepts and data to audiences of varying levels of scientific competency. Identify and manage potential new business through client management, relationship building, and problem solving. Develop and execute studies relevant to assays required for development and execution of Current Good Manufacturing Practice regulations (cGMP) manufacturing of Cell and Gene Therapy Products within the development matrix. Interact with new and existing Cell and Gene Therapy clients to document and transfer new protocols and procedures to Lonza sites and communicate and present the work in internal and client meetings. Design and review of experiments of assay optimization, qualification, validation, and trouble shoot the problems. Understand development of processes for manufacturing of Cell and Gene Therapy Products and implementation of appropriate in process control and monitoring assays into such processes. Provide technical and scientific leadership to other team members which includes, providing assistance to management in the design of new, unique or existing protocols. Support and lead the discussions around definition of scope of development work and resource planning. Establish and maintain a good working relationship within the operations department and other departments such as Research and Development (R&D), Quality Control (QC), Quality Assurance (QA) and Project Management (PM). Lead, review, train, assist in writing and revising technical documents including laboratory Standard Operating Procedures (SOPs), protocols, reports and batch records. Develop and execute state-of-the-art manufacturing processes for current Good Manufacturing Practices (cGMP) within the Cell Therapy Development matrix with minimal support from development manager. Utilize experience with cellular, biochemical and molecular techniques including cell culture, nucleic acid extraction, real time qPCR/RT-PCR, dd PCR, flow cytometry, microscopy, ELISA, spectrophotometric, and fluorometric cell-based potency assays. Oversee One(1) Scientist I. MINIMUM REQUIREMENTS: Requires a Master's degree, or foreign equivalent degree, in Medical Sciences or Biochemistry and Molecular Biology and 2 Years of experience in the job offered, or 2 Years of experience in a related occupation developing and executing state-of-the-art manufacturing processes for Current Good Manufacturing Practices (cGMP) within the Cell Therapy Development matrix with minimal support from development manager; utilizing experience with cellular, biochemical and molecular techniques including cell culture, nucleic acid extraction, real time qPCR/RT-PCR, dd PCR, flow cytometry, microscopy, ELISA, spectrophotometric, and fluorometric cell-based potency assays. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

About the Role: We are seeking a highly motivated Reservoir Simulation Research Scientist to contribute to the next generation of reservoir modeling technologies. This role focuses on the research and development (R&D) of advanced computational methods combining physics-based reservoir simulation with machine learning, data assimilation, and optimization. You will work on developing novel algorithms, enhancing simulation capabilities, and bridging data-driven and physics-based modeling approaches to support the energy transition and improve reservoir management workflows. Key Responsibilities: Conduct fundamental and applied research in reservoir simulation, computational physics, and data-driven methods. Develop and prototype novel algorithms that integrate machine learning with traditional reservoir simulation workflows, including surrogate modeling, reduced-order modeling, and hybrid physics-ML models. Research and implement advanced data assimilation techniques, including ensemble-based methods, adjoint-based gradient optimization, and Bayesian inference for history matching and uncertainty quantification. Develop and apply optimization algorithms for field development planning, production enhancement, and reservoir control under uncertainty. Collaborate with cross-disciplinary teams including reservoir engineers, geoscientists, data scientists, and software engineers. Publish research outcomes in peer-reviewed journals, patents, and present at industry and academic conferences. Provide technical leadership in framing R&D roadmaps, identifying high-impact research directions, and supporting technology transfer into commercial or operational tools. Contribute to the development of internal software prototypes or production-grade software for reservoir modeling and AI-enabled workflows. Required Qualifications: Ph.D. in Petroleum Engineering or Reservoir Engineering or a related field with a focus on numerical simulation, optimization, or machine learning applications. Strong background in numerical methods for PDEs, linear and nonlinear solvers, and reservoir flow physics. Expertise in reservoir simulation technologies, including finite difference, finite volume, or finite element methods applied to multiphase subsurface flow. Demonstrated research experience in one or more of the following: Machine learning (e.g., surrogate modeling, neural networks, Gaussian processes, physics-informed ML) Data assimilation (e.g., Ensemble Kalman Filter, Ensemble Smoother, Adjoint-based optimization, Bayesian inference) Optimization (e.g., field development planning, well control optimization, robust optimization under uncertainty) Proficiency in scientific programming (ideally Python and MATLAB) for algorithm development and prototyping. Proven track record of peer-reviewed publications, conference presentations, or patents in relevant technical domains. Preferred Qualifications: Experience integrating physics-based simulation with machine learning frameworks, including Physics-Informed Neural Networks (PINNs) or hybrid models. Knowledge of high-performance computing (HPC), parallel programming, or cloud computing for large-scale simulations. Familiarity with open-source or commercial reservoir simulators (e.g., MRST, Open Porous Media, Eclipse, Intersect, tNavigator, CMG). Experience with probabilistic modeling, uncertainty quantification, and decision-making under uncertainty. Background in related domains such as CO₂ sequestration, geothermal systems, or unconventional resources modeling is a plus. Soft Skills: Strong analytical and problem-solving skills with a rigorous scientific approach. Ability to communicate complex technical ideas clearly to both technical and non-technical audiences. Self-driven, collaborative, and passionate about advancing the state of the art in reservoir engineering and computational sciences. Comfortable working in both independent research settings and collaborative, multi-disciplinary environments. Why Join Us? Work on cutting-edge problems at the intersection of subsurface science, machine learning, optimization and computational physics. Be part of a collaborative R&D team influencing the future of energy, carbon management, and sustainable subsurface technologies. Opportunities to publish, patent, and contribute to open-source software or commercial products. Competitive compensation, research freedom, and professional growth in a dynamic, innovation-driven environment.

Full-time Description Job Title: Scientist I/II, PD - Downstream Department: PD and CRO Reports To: Associate Director FLSA Status: Full Time/Exempt Mission Statement The mission of PackGene Biotech is to accelerate gene therapy product development by providing an integrated one-stop shop solution to the gene therapy industry. We strive to make gene therapy accessible to more patients in needs. Gene therapy is believed to revolutionize the healthcare field in upcoming years. PackGene is well positioned to play a big role in this transformation. Company Background PackGene Biotech was founded in 2014 by a team of visionary scientists united by a common goal-to make life-changing gene therapies accessible to all. Witnessing the success of adeno-associated virus (AAV) vectors in restoring sight and hearing to patients, our team saw both the promise and the challenge: the high cost and complexity of vector production, which limited access to those who needed it most. Determined to overcome these barriers, we built PackGene to revolutionize AAV manufacturing with innovative, scalable, and cost-effective solutions. Our work has enabled life-changing therapies, including a young boy born with congenital deafness. After receiving an AAV-based treatment produced by PackGene, he began responding to his family's voices. A few months later, he spoke his first word: “Dad.” His father wept with joy-a moment that reminded our team why we do what we do. It was more than just science; it was about restoring hope and giving families a future. Today, PackGene is a global leader, serving clients in over 30 countries and partnering with more than 1,000 biopharmaceutical companies and research institutions. Our slogan, "Make Gene Therapy Affordable," reflects our unwavering mission. We focus on tackling key challenges in gene therapy development, including viral vector production and specific targeting, mRNA technologies, and GMP production at scale. We are committed to providing stable, qualified, cost-efficient, and fast services, along with technical support, to empower our gene therapy partners. Together, we aim to transform lives and build a healthier, better world. Requirements Duties and responsibilities Participate in planning and hands-on execution of lab operation activities, including new equipment acquisition, training and maintenance. Hands-on execution of downstream unit operations such as clarification and filtration, tangential flow filtration (TFF), chromatography purification with AKTA system and ultracentrifugation unit operations. Downstream process development and operation experience of viral vectors or protein/antibody therapeutics is strongly preferred. Maintain a high level of technical acumen in the field of viral vector downstream process. Participate in client meetings and serve as a downstream process subject matter expert (SME). Work with a cross-functional team to perform technology transfer of downstream procedures into GMP. Ability to pass gowning training and support GMP operations in cleanrooms Design and execute downstream development studies, involving suspension and adherence platform process. Occasional weekend work may be required. Perform timely data acquisition, analysis and troubleshooting; report project progress in cross-functional team meetings. Ability to troubleshoot process and equipment, and support deviation investigations and make scientifically sound decisions Draft and review technical documents such as protocols, technical reports, and risk assessments. Ability to perform scientific review of master batch records and SOPs. Ability to create and review Unicorn methods for accuracy. Ensure timeline adherence Coach of junior associates on experimental rationale, design, execution and troubleshooting. High level of accountability, integrity and communication; foster a culture of collaboration, trust, and teamwork. Build strong and cohesive working relationships with colleagues from other teams to accomplish company goals. Skills and Qualifications Ph.D. or M.S. in Biology, Biotechnology, Engineering, or other gene therapy-related field. 1-4+ years for Ph.D. or 4-8 years for M.S. of industrial experience in Biologics development, including protein, antibody, and viral vectors (AAV, or lentiviral vector). Proficient in QbD based approach utilizing Design of Experiments (DOE). Working knowledge of GMP, FDA-regulated industry. Demonstrated ability to work cross functionally in multi-disciplinary teamwork. Proficient in MS Office suites of products. Ability to multitask, prioritize work independently. Capable of analyzing problems and finding solutions. Ability to work under pressure while maintaining a professional manner. Other duties as assigned. Working conditions Onsite location with occasionally sitting at a desk as well as frequently walking and standing in the lab to perform lab work. Physical requirements Crouching: Bending the body downward and forward by bending leg and spine. Hearing: Perceiving the nature of sounds at normal speaking levels with or without correction and having the ability to receive detailed information through oral communication and making fine discriminations in sound. Kneeling: Bending legs at knee to come to a rest on knee or knees. Lifting: Raising objects of 25lbs from a lower to a higher position or moving objects horizontally from position to position. This factor is important if it occurs to a considerable degree and requires the substantial use of the upper extremities and back muscles. Pulling: Using upper extremities to exert force in order to draw, drag, haul or tug objects in a sustained motion. Pushing: Using upper extremities to press against something with steady force in order to thrust forward, downward or outward. Reaching: Extending hand(s) and arm(s) in any direction. Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers. Sitting: Sitting for a period of time. Standing: Remaining upright on the feet, particularly for sustained periods of time. Stooping: Bending body downward and forward by bending spine at the waist. Talking: Expressing or exchanging ideas by means of the spoken word; those activities where detailed or important spoken instructions must be conveyed to other workers accurately, loudly, or quickly. Walking: Moving about on foot to accomplish tasks, particularly for long distances or moving from one work site to another. The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading; visual inspection involving small defects, small parts, and/or operation of machines (including inspection); using measurement devices; and/or assembly or fabrication of parts at distances close to the eyes.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Lonza is currently seeking an experienced Scientist II, BioAssay Services to join their team in Houston, TX. POSITION: Scientist II, BioAssay Services JOB LOCATION: 14905 Kirby Dr, Houston, TX 77047 DUTIES: Design analytical methodology for the characterization of Cell and Gene Therapies. Execute analytical testing to characterize Cell and Gene Therapy drug products/substances. Validate analytical methodology for the characterization and release of Cell and Gene Therapies. Transfer analytical methodologies to the quality control laboratory and train quality control analysts. Lead client discussion and drive project direction. Manage project timelines and delivery. Lead a project team in a matrix organization to deliver projects on-time and in-full. Develop junior scientists analytical capability through direct on-the-job training and mentorship. Present and explain complex scientific concepts and data to audiences of varying levels of scientific competency. Identify and manage potential new business through client management, relationship building, and problem solving. Develop and execute studies relevant to assays required for development and execution of Current Good Manufacturing Practice regulations (cGMP) manufacturing of Cell and Gene Therapy Products within the development matrix. Interact with new and existing Cell and Gene Therapy clients to document and transfer new protocols and procedures to Lonza sites and communicate and present the work in internal and client meetings. Design and review of experiments of assay optimization, qualification, validation, and trouble shoot the problems. Understand development of processes for manufacturing of Cell and Gene Therapy Products and implementation of appropriate in process control and monitoring assays into such processes. Provide technical and scientific leadership to other team members which includes, providing assistance to management in the design of new, unique or existing protocols. Support and lead the discussions around definition of scope of development work and resource planning. Establish and maintain a good working relationship within the operations department and other departments such as Research and Development (R&D), Quality Control (QC), Quality Assurance (QA) and Project Management (PM). Lead, review, train, assist in writing and revising technical documents including laboratory Standard Operating Procedures (SOPs), protocols, reports and batch records. Develop and execute state-of-the-art manufacturing processes for current Good Manufacturing Practices (cGMP) within the Cell Therapy Development matrix with minimal support from development manager. Utilize experience with cellular, biochemical and molecular techniques including cell culture, nucleic acid extraction, real time qPCR/RT-PCR, dd PCR, flow cytometry, microscopy, ELISA, spectrophotometric, and fluorometric cell-based potency assays. Oversee One(1) Scientist I. MINIMUM REQUIREMENTS: Requires a Master's degree, or foreign equivalent degree, in Medical Sciences or Biochemistry and Molecular Biology and 2 Years of experience in the job offered, or 2 Years of experience in a related occupation developing and executing state-of-the-art manufacturing processes for Current Good Manufacturing Practices (cGMP) within the Cell Therapy Development matrix with minimal support from development manager; utilizing experience with cellular, biochemical and molecular techniques including cell culture, nucleic acid extraction, real time qPCR/RT-PCR, dd PCR, flow cytometry, microscopy, ELISA, spectrophotometric, and fluorometric cell-based potency assays. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

ARTIDIS is a clinical-stage health-tech start-up founded in Basel, Switzerland, that has developed the first nanomechanical biomarker for cancer diagnosis and treatment optimization. The ARTIDIS nanotechnology platform integrates different types of clinical data into the ARTIDISNET digital platform, allowing physicians to significantly shorten the current diagnostic process and benefit both the patient and the healthcare system. ARTIDIS enables professionals to design personalized cancer treatment plans tailored to individual patients' needs and desired outcomes. Job Purpose We are seeking an AFM Scientist to join our Application Support team. In this role, you will leverage your advanced AFM expertise to support pre-clinical and clinical operations, develop and optimize measurement protocols, and ensure the highest standards of data quality, reproducibility, and regulatory compliance. You will work closely with research teams, clinical partners, and customers to deliver exceptional support, training, and troubleshooting. This position requires 100% on-site availability and approximately 50% travel within the USA. Duties and Responsibilities Conduct pre-clinical and clinical AFM-based research to characterize the nanomechanical properties of solid tumors. Develop and refine measurement protocols, including sample preparation methods, measurement standards, and custom specimen holder design. Optimize and execute measurement routines both at ARTIDIS facilities and customer sites. Prepare technical documentation, study reports, work instructions (WIs), and test plans in compliance with FDA regulations and ISO 13485 standards. Provide on-site support and troubleshooting for clinical and research teams, adapting to hospital and laboratory schedules. Improve AFM data analysis pipelines, conduct advanced statistical analyses, and support analytical validation testing. Validate the performance of new devices and measurement tools on biological samples in clinical settings. Develop training protocols and education for internals and externals. Gather and document user requirement and feedback to guide ongoing development and product improvements. Maintain strong relationships with hospital partners and customers through regular site visits and workflow support. Qualifications Ph.D. or equivalent in Physics, Biomedical Engineering, Materials Science, or a related field with a focus on AFM or scanning probe microscopy. Proven experience in AFM measurements of biological samples, tissue/cell nanomechanics, sample preparation, and quantitative data analysis. Familiar with medical device operations, ISO 13485, FDA guidelines, CE Marking, and international regulatory frameworks. Skilled in technical training, application support, and tailoring AFM solutions to end-user needs. Strong ability to troubleshoot AFM systems, optimize measurement workflows, and collaborate in multidisciplinary environments. Willingness and ability to travel frequently in the USA. Excellent written and verbal skills for technical documentation, presentations, and scientific discussions. Ability to manage multiple AFM-related projects in a fast-paced, evolving environment. Working Conditions You will join a highly motivated international team in a dynamic start-up environment. This role offers the opportunity to rapidly expand your expertise, take ownership of critical AFM projects, and contribute to impactful cancer research. We value initiative, direct communication, and a team spirit that goes the extra mile. Your efforts will be rewarded with challenging projects, meaningful contributions to patient care, and a competitive compensation package with performance-based bonuses.

Roger Trinh Talent Solutions is partnering with a growing Houston-based contract manufacturing company. Our client seeks a Scientist I to join their product development team in collaboration with Roger Trinh Talent Solutions. The Scientist will be responsible for developing robust processes for formulation, fill and finish, and cryopreservation of chimeric antigen receptor T (CAR T) and Tumor-Infiltrating Lymphocytes (TIL) cell products. The ideal candidate will be an internal expert in cellular cryopreservation and cryobiology and stay current on advancements in the field. Proficiency in Cryobiologist and Cryopreservation experience with cell therapy drug development (working with different reagents) is required. Key Responsibilities: Developing solid processes for the formulation, fill and finish, and cryopreservation of CAR T and TIL cell products. Conducting studies on these products' formulation, fill/finish, and cryopreservation. Evaluating new cryobiological technologies. Implementing process advancements for scaling up and introduction into a GMP manufacturing environment. Leading technology transfer activities and training manufacturing staff on new processes and equipment. Monitoring process performance during clinical manufacturing via data tracking, trending, and analysis. Designing and conducting experiments in the development laboratory to support process changes, generate process robustness data, and resolve manufacturing non-conformances. Drafting technical documents, including development reports, process descriptions, risk assessments, SOPs, MBRs, and regulatory filing sections Acting as an internal expert, maintaining state-of-the-art cellular cryopreservation and cryobiology knowledge, and performing other duties as assigned. Requirements: Ph.D. in a related scientific/engineering field preferred, or master's degree with 5+ years' experience in a related field, preferably in the biotech industry or equivalent combination of education and experience. Strong knowledge and hands-on experience with cell therapy process development and cryopreservation. Highly desired experience: Formulation science experience with cryoprotectant additives. Demonstrated aseptic cell handling skills. Experience working in or supporting a cGMP-regulated environment. Hands-on experience with standard cell therapy laboratory equipment and technology platforms Familiarity with the following is a plus: Solid background in cell therapy manufacturing processes. Proficient with MS Office (Excel, Outlook, etc.) and statistical software (Prism, JMP). Strong scientific understanding of the fundamental principles of cryopreservation and cell therapy. Demonstrated ability to collaborate effectively in a multi-disciplinary team. Demonstrated strong communication skills, interpersonal skills, and a superior drive for results. Excellent written, oral, interpersonal, and presentation skills and the ability to effectively interface with senior management and staff. Excellent judgment and creative problem-solving skills, including negotiation and conflict resolution skills.

Who we are? United Imaging is a leading global medical device developer and supplier with a diversified portfolio of advanced medical products, digital healthcare solutions, and intelligent solutions that cover the entire process of imaging diagnosis and treatment. From our North American HQ in Houston, we are passionate about expanding our customer sales and support structure, embracing the highest quality and craftsmanship in each of our medical imaging products, and dedicated to building an outstanding organization. Join our innovative team with the mission of developing and supplying advanced technologies and improving patient care worldwide. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Company Website: ************************************** Benefits When joining our team, we offer the following benefits: medical, dental, vision, short- & long-term disability insurance, employee assistance program, company paid basic life insurance, 401(k) with employer match, paid time off, sick leave, and paid holidays. For on-site positions, relocation assistance will be provided as needed. Duties & Responsibilities As a CT Algorithm Research Scientist, major responsibilities will include, but are not limited to: Develop and implement advanced imaging algorithms for CT clinical applications, scientific research, and pre-clinical studies. Demonstrate the effectiveness and accuracy of the algorithms using appropriate quantitative metrics. Participate in the development of research and development plans for advanced CT products. Collaborate with internal development teams and research partners for the comprehensive evaluation and testing of prototypes and new products. Maintain clinical and technical expertise. Regularly share up-to-date knowledge of new developments in the CT imaging field within the group and actively seek out new opportunities for research project development. Review and evaluate mature technologies for potential incorporation into medical imaging products. Participate in publication of results at conferences and in peer-reviewed journals. Protect innovations with invention disclosures. Requirements Education PhD in Biomedical Engineering, Medical Physics, Computer Science, Electrical Engineering, Data Science, or related fields. Experience CT research experience with a proven track record of scientific publications. Background in medical imaging, artificial intelligence, and/or clinical experience is preferred. Required Skills or/ Attributes Excellent communication and presentation skills. Strong communication skills with great ambition. Desire to learn, ask questions, and be resourceful in identifying innovative applications and creative solutions to complex problems. Willing and able to travel up to 25%, including short-term international trips. Working Conditions: Magnetic Environment Exposure: This position requires working in an environment where strong magnetic fields may be present. Employees may be exposed to powerful magnets, electromagnetic equipment, or other devices that generate magnetic fields. Risk to Ferrous Metals in the Body: Due to the nature of the magnetic environment, employees must not wear or carry ferrous metals on their person while in the designated work area. This includes, but is not limited to, metal objects such as steel, iron, and other ferrous materials. Additionally, employees with implants, medical devices, or foreign objects containing ferrous metals within their body (e.g., certain surgical implants, pacemakers, or metal pins) may be at risk and must disclose any such conditions to their supervisor prior to starting work. Diversity, Equity, and Inclusion United Imaging is an Equal Opportunity Employer. Diversity, equity, and inclusion matter. United Imaging provides equal employment opportunities to all applicants for employment and prohibits discrimination and harassment of any type with regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.*Note: Relocation is not available for this role.

"Bridging Innovation to Cure" Developing and Manufacturing your cell therapies from benchtop to bedside Cellipont Bioservices is growing, and we are looking for a Scientist II, Analytical Development who believe in the potential bridging clients discoveries to patient cures and who want to challenge the status quo and take Cellipont and it's clients to the next level. The Scientist II, Analytical Development will participate in activities of development, tech transfer, qualification, validation, and automation of analytical methods to support client product manufacturing activities. This position plays a key role demonstrating the values, culture, and deliverables for the site. The Role Ability to work semi-independently, executing and analyzing experiments for multiple projects to support process development, product characterization, in-process monitoring, stability testing, and GMP manufacturing. Act as technical subject matter expert (SME) for the company, leading and participating in developing, transferring, and qualifying cell therapy methods, including flow cytometry, ELISA, q-PCR/dd PCR, and/or cell-based assays. Co-lead the development of automated QC methods for high-throughput sample testing, including the preparation, purification, and nucleic acid amplification. Work collaboratively with the AD, Process Development and Quality Control team members in the execution, documentation, and transfer of analytical methods. Writes and reviews Standard Operating Procedures (SOPs), protocols, and associated reports as needed. Experience presenting technical project status and data-driven updates to internal teams and clients. Responsible for remaining current with GMP/GLP/GDP, ICH, USP, and FDA guidelines, industry standards, and trends that apply to current and future Cell Therapy Development operations and products. Assess, support, and implement new analytical technologies and fill the technical gaps within Cellipont. Provides support in aspects of Laboratory Investigations, CAPAs, Change Control, and Quality Records. Domestic or international travel maybe be required. The Candidate Bachelor's Degree minimum in Biological Science, Biochemical Engineering, or related science preferred with a minimum of 5+ years of laboratory experience in R&D or Analytical Development within academia and/or direct industry environment. Master's Degree preferred with a minimum of 2+ years of laboratory experience in R&D or Analytical Development within academia and/or direct industry environment. D. preferred with a minimum of 1+ years of laboratory experience in R&D or Analytical Development within academia and/or direct industry environment. Demonstrated expertise in a range of analytical methods used in cell therapy, including flow cytometry, ELISA, q-PCR/dd PCR, and/or cell-based assays required. Experience in operating automated laboratory equipment is preferred. Attention to detail, problem-solving ability, and troubleshooting assays and instrumentation are required. Ability to apply problem-solving skills, work in a high-paced team environment, multitask activities, meet deadlines, and prioritize work on multiple projects. Ability to effectively present information to top management, public groups, and/or clients. Excellent interpersonal skills with the ability to work individually and as part of a multifunctional team. Position Benefits Opportunities for career growth within an expanding team. Defined career path and annual performance review & feedback process. Cross-functional exposure to other areas of within the organization. Robust benefit package designed for unique Health & Wellness needs, including coverage for your furry family members. 401K strong employer match. Tuition Reimbursement. Employee Referral Bonuses. Flexible work schedules and PTO based on role/level, increasing 1 PTO day each year and paid holidays Gain experience in the cutting-edge cell therapy space "At Cellipont Bioservices, we look for candidates with an innate desire to serve. Our "family" approach ensures you will get the mentorship you need to develop a satisfying career here!" Notice to Agency and Search Firm Representatives Cellipont Bioservices is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Cellipont Bioservices employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Cellipont Bioservices. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

UTHealth Houston's Psychiatry and Behavioral Sciences is hiring a Postdoctoral Research Fellow who will support a translational neuroscience laboratory investigating mechanisms linking Alzheimer's disease (AD), sepsis-associated encephalopathy, systemic inflammation, neuroimmune interactions, and long-term cognitive impairment. The position involves work with animal models (including the CLP sepsis model), human clinical samples, and a broad range of molecular, behavioral, and imaging techniques. The candidate should possess strong technical skills, including immunofluorescence (IF), immunohistochemistry (IHC), confocal imaging, and quantitative analysis of tissue sections. They should also be able to perform rodent behavioral tasks using the Any-maze tracking system (e.g., open field, Y-maze, fear conditioning), actively participate in the CLP sepsis procedure and related in vivo work, and analyze data using GraphPad Prism and other standard analytical software. Applicants must submit reference information/letters of recommendation for at least two professional references; one of the references may be the candidate's doctoral mentor. What we do here changes the world. UTHealth Houston is Texas' resource for healthcare education, innovation, scientific discovery, and excellence in patient care. That's where you come in. Once you join us you won't want to leave. It's because we reward our team for the excellent service they provide. Our total rewards package includes the benefits you'd expect from a top healthcare organization (benefits, insurance, etc.), plus: * 100% paid medical premiums for our full-time employees * Generous time off (holidays, preventative leave day, both vacation and sick time - all of which equates to around 37-38 days per year) * The longer you stay, the more vacation you'll accrue! * Build your future with our awesome retirement/pension plan! We take care of our employees! As a world-renowned institution, our employees' wellbeing is important to us. We offer work/life services such as... * Free financial and legal counseling * Free mental health counseling services * Gym membership discounts and access to wellness programs * Other employee discounts including entertainment, car rentals, cell phones, etc. * Resources for child and elder care * Plus many more! Position Summary: A biomedical postdoc position provides an opportunity for early-career researchers to gain valuable experience, develop independent research skills, and contribute to the advancement of scientific knowledge in their field of expertise. Position Key Accountabilities: * Plans and conducts experiments, analyzes data, and prepares publications describing results. * Assists in training and mentoring of lab personnel, including graduate students and other trainees. * Reads and evaluates literature. * Possess interpersonal skills to effectively collaborate and communicate with individuals at all levels. * Have strong written and oral communication skills. * Animal Models & In Vivo Procedures * Perform rodent handling, habituation, health monitoring, and husbandry tasks following IACUC guidelines. * Conduct Cecal Ligation and Puncture (CLP) surgery to model sepsis, including pre-operative and post-operative care, analgesia, fluid therapy, and survival monitoring. * Assist with transponder implantation, antibiotic treatment, fluid resuscitation, and humane endpoint evaluation. * Perform euthanasia, perfusion, and careful dissection of brain, CSF, blood, spleen, liver, lung, and gastrointestinal tissues. * Behavioral Neuroscience Testing * Conduct behavioral testing using Any-maze video tracking software, including: Open Field Test (locomotion/anxiety), Y-Maze (working memory), Novel Object Recognition, Contextual & Cued Fear Conditioning, SHIRPA neurological battery * Analyze behavioral outcomes, perform data cleaning, and generate tracking heat maps and statistical outputs. * Clinical Sample Processing * Receive, log, and process human biological samples, including plasma, serum, CSF, PBMCs, saliva, and stool from clinical collaborators. * Perform centrifugation, aliquoting, cryopreservation, and biobanking following established SOPs and biosafety guidelines. * Assist in clinical database management and maintain strict tracking of participant metadata, sample IDs, and storage locations. * Molecular & Cellular Assay * Prepare tissue homogenates for ELISA, Western blot, qPCR, multiplex cytokine/chemokine profiling, and biochemical marker analysis (e.g., GFAP, NfL, Aβ, pTau). * Isolate extracellular vesicles (EVs) using ultracentrifugation, differential centrifugation, or size-exclusion chromatography (IZON qEV columns). * Performs other duties as assigned. Minimum Education: Doctoral/Terminal Degree Experience preferred: * Laboratory Experimental Work * Immunofluorescence (IF) and Immunohistochemistry (IHC) * Confocal and Keyence Microscope Operation * Data Management and Analysis Physical Requirements: Exerts up to 20 pounds of force occasionally and/or up to 10 pounds frequently and/or a negligible amount constantly to move objects. Security Sensitive: This job class may contain positions that are security sensitive and thereby subject to the provisions of Texas Education Code § 51.215 Residency Requirement: Employees must permanently reside and work in the State of Texas.

Reports to: Research & Development Manager Do You Dream of Working in a Fast-Paced Environment Where Your Initiative Drives Success? Are You Ready to Drive Change Through Innovation and Responsible Action? The Color Scientist is responsible for supporting the development, matching, and maintenance of color formulations within the coatings segment. This role ensures accuracy, consistency, and efficiency in color processes through technical execution, database management, and cross-functional collaboration. The Color Scientist provides insight to internal teams, distributors, and customers while contributing to continuous improvement initiatives and supporting commercial/regional projects. Do You Want to Be Part of a Global Team Where Collaboration Drives Success? What you need to be successful in this role: Execution-oriented: delivers tasks with precision and timeliness. Collaborative: partners with peers, distributors, and cross-functional teams. Technical: focuses on accuracy of formulas, testing, and data. Supportive: assist with training and documentation but does not own strategy or leadership responsibilities Adaptability- Demonstrates adaptability and resilience by effectively adjusting to frequent changes in priorities, systems, and processes, while embracing new implementations to ensure continued alignment with organizational objectives. Key Responsibilities Execute color development, color matching, and tinting requests for R&D, distributors, customers and commercial. Support maintenance of color databases (Synergy T3, LargoMatch, LargoTint, etc.), ensuring formulas are accurate, current, and aligned with regional/global standards. Conduct testing, evaluation, and troubleshooting of color formulations to resolve technical issues including customer complaints. Conduct database audits, identifying and correcting shade duplications, missing reflectance data, or misalignments. Support distributor launches by preparing formulas, files, and training materials. Support product launches as needed based on color database requirements Collaborate with cross-functional teams (R&D, Technical Service, Operations, Marketing, Sales) to deliver color solutions. Assist with training, documentation, and technical support to internal staff and distributor personnel. Contribute to the development of SOPs and knowledge-transfer documents for sustainable processes. Participate in projects aimed at improving efficiency, standardization, optimization, and productivity in alignment with global color lab systems. Independently work and manage multiple projects with varying timelines. Troubleshoot color database related issues at off-site locations Travel requirement Qualifications Bachelor's degree in chemistry, Materials Science, or related field (or equivalent technical experience). Color matching and color theory experience is required 2-4 years of experience in a coatings or chemical manufacturing environment with focus on color matching, tinting, or formulation. Hands-on experience with color database software and spectrophotometer. Strategic thinker with a detail-oriented and proactive approach. Proficiency in spoken English and Spanish is considered a plus. Team members have the option to work a 4/10 schedule - four 10-hour days per week with one weekday off. Please note, we do not offer sponsorship for this role. Must be authorized to work in the US. Sounds like a match? Welcome to apply! Click the ‘Apply for position' button at the top of the page and submit your application letter with a CV in English via our recruitment system. Application due 2026-01-30 Seniority Level Associate Job Functions Production, Product Management, Research Industry Chemicals At Hempel, you're welcomed to a global community of +7000 colleagues around the world. A workplace built on shared trust, mutual respect and support for each other. We're on a mission to double our impact. To succeed, we need bright minds and team players. Which is why, from day one, your input, ideas and initiative are not only welcomed, but expected. In return, you will enjoy great opportunities for development in a growing global company - and be part of the solution by contributing to our global impact. At Hempel, we are committed to everyone feeling safe, valued and treated equally, in an environment where each employee can bring their authentic selves to work. We believe that inclusion is key to innovation and by bringing together the most diverse perspectives and talents, we can achieve great things, together.

**Have you ever thought about being part of a company that reimagines chemistry every day to build a better world?** That's the purpose of Indorama Ventures, and we want you with us on this journey! We are looking for innovative, collaborative professionals who are ready to embrace the challenge of working in a company that is constantly expanding internationally. We value flexibility, partnership, and believe that the impact of our actions goes far beyond the chemical industry. Here, diversity matters. Our work environment is inclusive, diverse, and guided by respect, ethics, and equal opportunities for all. **What we're looking for:** **What will be expected from you?** + Set up and execute laboratory to meet both internal and external customer expectations. + Developing methods to analyze samples or the applications testing to prove claims, + Maintain an awareness of the literature and other sources of information to remain current with developments in the area of functional products of interest to the Corporation. + Work with the sales force to evaluate, select, and apply standard chemistry techniques and procedures to solve customer or company objectives under the direction of the R&D management. + Able to present results to internal and external customers. + Present work at public forums like conferences. + Work projects in PMOx (project management system) + Preparing internal and customer document, reports, and presentations + Keep neat and orderly notebooks containing a record of all work performed. Maintain other records as necessary to support patent applications for innovative products. + Maintain orderly laboratory space, + Follow all safety and training requirements, + Stay with budget targets. + Manage and optimize all process under your responsibility taking into consideration Quality, Legality and Food Safety (if applicable) and client needs on Indorama's products and services. + Guarantee all documentation under your responsibility updated and available for consulting. + Interact with R&D team to improve the lab, lab methods, etc. **What are we looking for in the ideal candidate?** + BS in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry/Engineering required plus 6 years relevant experience. + M.S. in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry/Engineering with 4 years relevant experience in the chemical field, or + Ph. D. in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry/Engineering with no commercial experience in the chemical field. + 1-6 years' experience (more 5 years' experience preferred) in: + R&D laboratory preferred, Surfactants knowledge in laboratory or application use strongly preferred, + Use and knowledge of Parr Reactors preferred for scientists in process area or + Market applications specific knowledge required in agriculture, crop solutions, or biosolutions for scientists in market segment areas. + Excellent organizational and communications skills + Computer literacy w/ databases, word processing, spreadsheets + Demonstrated presentation skills required. + English with Bilingual Portuguese or Spanish strongly preferred. **What do we offer?** A competitive compensation package, including: - Health insurance - WellHub / TotalPass - Life insurance - And other exclusive benefits The division you'll be joining is a global leader in the chemical industry. We offer a broad portfolio of solutions and high delivery standards to markets such as Crop Solutions, Home and Personal Care, Coatings, Energy & Resources, and Performance Products. **Here, you can make a difference.** **Join us!** We're Indovinya, a top producer of chemical intermediates and surfactants. Our extensive portfolio is designed to meet our customers' most diverse needs. As producers of solutions used for crops, oil and gas, coatings, home and personal care, and other applications, we are present in the daily lives of millions worldwide. Through our increasingly sustainable chemistry, designed to meet the needs of each of our customers carefully, we want to transform our operations and products into something increasingly relevant for the planet. We are part of Indorama Ventures Public Company Limited, one of the world's leading petrochemical producers, and are present globally with manufacturing in Europe, Africa, Americas, and Asia-Pacific. With 18 plants, seven R&D centers, and an experienced management team, we have a strong track record of environmental stewardship. Our expertise lies in innovative, eco-friendly chemistry. Today, Indovinya emerges as a more robust and strategic company dedicated to driving new business opportunities while prioritizing the well-being of countless individuals as employees, customers, suppliers and mainly the communities close to our operations worldwide.

Have you ever thought about being part of a company that reimagines chemistry every day to build a better world? That's the purpose of Indorama Ventures, and we want you with us on this journey! We are looking for innovative, collaborative professionals who are ready to embrace the challenge of working in a company that is constantly expanding internationally. We value flexibility, partnership, and believe that the impact of our actions goes far beyond the chemical industry. Here, diversity matters. Our work environment is inclusive, diverse, and guided by respect, ethics, and equal opportunities for all. What we're looking for: What will be expected from you? Set up and execute laboratory to meet both internal and external customer expectations. Developing methods to analyze samples or the applications testing to prove claims, Maintain an awareness of the literature and other sources of information to remain current with developments in the area of functional products of interest to the Corporation. Work with the sales force to evaluate, select, and apply standard chemistry techniques and procedures to solve customer or company objectives under the direction of the R&D management. Able to present results to internal and external customers. Present work at public forums like conferences. Work projects in PMOx (project management system) Preparing internal and customer document, reports, and presentations Keep neat and orderly notebooks containing a record of all work performed. Maintain other records as necessary to support patent applications for innovative products. Maintain orderly laboratory space, Follow all safety and training requirements, Stay with budget targets. Manage and optimize all process under your responsibility taking into consideration Quality, Legality and Food Safety (if applicable) and client needs on Indorama's products and services. Guarantee all documentation under your responsibility updated and available for consulting. Interact with R&D team to improve the lab, lab methods, etc. What are we looking for in the ideal candidate? BS in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry/Engineering required plus 6 years relevant experience. M.S. in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry/Engineering with 4 years relevant experience in the chemical field, or Ph. D. in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry/Engineering with no commercial experience in the chemical field. 1-6 years' experience (more 5 years' experience preferred) in: R&D laboratory preferred, Surfactants knowledge in laboratory or application use strongly preferred, Use and knowledge of Parr Reactors preferred for scientists in process area or Market applications specific knowledge required in agriculture, crop solutions, or biosolutions for scientists in market segment areas. Excellent organizational and communications skills Computer literacy w/ databases, word processing, spreadsheets Demonstrated presentation skills required. English with Bilingual Portuguese or Spanish strongly preferred. What do we offer? A competitive compensation package, including: • Health insurance • WellHub / TotalPass • Life insurance • And other exclusive benefits The division you'll be joining is a global leader in the chemical industry. We offer a broad portfolio of solutions and high delivery standards to markets such as Crop Solutions, Home and Personal Care, Coatings, Energy & Resources, and Performance Products. Here, you can make a difference. Join us!

Research Scientist I, Moody Brain Health Institute - (2505969) Description JOB DESCRIPTION: The Research Scientist will lead research and development focused on digital twin modeling for brain health and health trajectory prediction within the Moody Brain Health Institute. This role involves designing, implementing, and validating computational models that simulate individual brain and health states across the lifespan. The scientist will integrate multi-modal patient data, including neuroimaging, electrophysiology, genomics, digital biomarkers, and electronic health records (EHRs), to create predictive digital twins capable of informing early diagnosis, personalized interventions, and resilience modeling. The position combines data science, neuroscience, and translational health research to advance precision brain health. They will also contribute to development of grant proposals, and scholarly publications. ESSENTIAL JOB FUNCTIONS:Execute the core's research initiatives, advancing key projects and objectives. Design and implement predictive models based on patient data to support research and clinical applications. Lead the development of virtual patient models to advance personalized medicine and data-driven research. Develop comprehensive data extraction strategies for Electronic Health Record (EHR) data, ensuring efficient and accurate analysis. Integrate multi-scale data sources such as neuroimaging, omics, cognitive, behavioral, and EHR data to build comprehensive individual-level representations. Present research findings and core activities at both internal and external conferences, symposia, and workshops. Support grant applications and publications, highlighting innovations in digital twin technologies for brain health. Contribute to infrastructure planning, including computing resources, secure data management, and AI model governance. Partner with the core director to plan resources and training for the development of AI tools and technologies. KNOWLEDGE/SKILLS/ABILITIESExcellent communication and interpersonal skills with a high degree of professionalism. Experience with high-throughput data analysis. Proficiency in AI, deep learning, and data fusion techniques for multimodal health data. Familiarity with federated or privacy-preserving learning for healthcare applications. Excellent communication and collaboration skills, with the ability to convey complex bioinformatics concepts to non-experts. Strong analytical skills and a proactive approach to problem resolution. Excellent decision-making skills. MINIMUM QUALIFICATIONS:PhD in Bioinformatics, Data Science, Biomedical Informatics, or a related biomedical field. Proven experience in Artificial Intelligence and/or statistical modeling, Familiarity with EHR data extraction, and analysis. Excellent communication skills and ability to collaborate with interdisciplinary teams. PREFERRED QUALIFICATIONS: Experience in working with AI and machine learning models, particularly in the biomedical context. Experience in digital twin frameworks, personalized modeling, or health trajectory prediction. Proven ability to lead collaborative, data-driven projects across disciplines. Prior involvement in leading or managing research projects. SALARY:Commensurate with experience. Qualifications EQUAL EMPLOYMENT OPPORTUNITY:UTMB Health strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. As a Federal Contractor, UTMB Health takes affirmative action to hire and advance protected veterans and individuals with disabilities. Primary Location: United States-Texas-GalvestonWork Locations: 0624 - Basic Science Bldg 301 University Blvd. Basic Science Building, rm. 120 Galveston 77555-0624Job: Research Academic & ClinicalOrganization: UTMB Health: RegularShift: StandardEmployee Status: Team Lead / TechnicalJob Level: Day ShiftJob Posting: Jan 12, 2026, 5:37:35 PM

Job Description Kindbody is a leading fertility clinic network and family-building benefits provider, delivering comprehensive reproductive care across the U.S. Our mission is to make fertility and family-building more accessible and affordable while ensuring superior health outcomes through clinical excellence and a seamless patient experience. About the Role As a Senior Embryologist at Kindbody, you will be working in a fast-paced, rapidly growing environment where you will be relied on for your expertise, professionalism, and collaboration. We consider our Senior Embryologists to be someone who is fully trained & signed off in all aspects of Embryology (basic + micro manipulation) for 6+ years. Responsibilities Perform Chemistry Laboratory and Andrology Laboratory Procedures as needed. Perform assisted reproductive technology methods, including but not limited to semen preparation, oocyte identification, conventional IVF, ICSI, embryo culture and grading, laser-assisted hatching, trophectoderm biopsy, sperm, oocyte, and embryo cryopreservation (vitrification). Maintain accurate laboratory records Perform quality control procedures and monitor KPIs Participate in the laboratory's quality management program Coordinate with reproductive endocrinologists and OB/GYNs to assist their patients with reproductive health issues and clinical research. Communicate with patients on outcomes, lab procedures, and general patient lab-related questions as needed Ensure all patient information is documented appropriately in our EMR according to our procedures Works independently to ensure the program goals are achieved Support and promote excellence in customer service Provide feedback to HQ on process improvement and job specifications to help gain efficiencies in the day-to-day Is willing to travel to other Kindbody locations to perform patient testing, train or support staff. Is willing to collaboratively support the Kindbody team remotely or locally with their expertise. Assist with projects, tasks, and team support as needed. Who You Are 6+ years experience in clinical embryology {3-4 of which are micromanipulation} TS (ABB) certified or eligible Able to work independently with minimal supervision Proficiency in all IVF laboratory methods, including micromanipulation techniques and vitrification Detail-oriented, meticulous record-keeping Strong communication skills & a team player Willingness to be flexible Familiarity with all state and local regulations, including tissue bank licensing Experienced in EMR and G-Suite