Senior principal scientist jobs in League City, TX

Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood! You won't find a work culture and benefits package like ours every day. Come join our team and a group of colleagues who love working at Castle! Learn more at ************************* Castle Biosciences Inc. is growing, and we are looking to hire a full-time R&D, Senior Scientist working from our Friendswood, TX office location, with a start date of February 1, 2026. Why Castle Biosciences? Exceptional Benefits Package: * Excellent Annual Salary + 20% Bonus Potential * 20 Accrued PTO Days Annually + 10 Paid Holidays * 401K with 100% Company Match up to 6% * 3 Health Care Plan Options + Company HSA Contribution * Company Stock Grant Upon Hire A DAY IN THE LIFE OF A Senior Scientist The Senior Scientist will work with R&D colleagues to develop evidence to support launched products in dermatology, while also collaborating across Castle Biosciences to produce key scientific materials such as publications, abstracts, slide decks, and other literature for internal training and external education. This role will spend the most time on data analysis, data presentation, collaboration with Marketing, Sales, and Medical Affairs, as well as publication planning, writing, and editing. REQUIREMENTS * PhD level training in life sciences * Experience related to Atopic Dermatitis preferred * The ability to successfully communicate and teach in a complex and competitive environment. * Strong interpersonal, organizational, and communication skills, written and oral. * Demonstrated team player. SCHEDULE * Monday - Friday, in-office 5 days a week from 9:00 am to 5:30 pm, exempt position, working from the Friendswood, TX office. * Off-hour work will be required to facilitate communication and meet deadlines. READY TO JOIN OUR BIOTECH TEAM? We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon! Castle Biosciences Awards and Research Developments! WORK AUTHORIZATION All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas. ABOUT CASTLE BIOSCIENCES INC. At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes. Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development. Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail ReasonableAccommodationsRequest@castlebiosciences.com. This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. No third-party recruiters, please

Thales people architect identity management and data protection solutions at the heart of digital security. Business and governments rely on us to bring trust to the billons of digital interactions they have with people. Our technologies and services help banks exchange funds, people cross borders, energy become smarter and much more. More than 30,000 organizations already rely on us to verify the identities of people and things, grant access to digital services, analyze vast quantities of information and encrypt data to make the connected world more secure. Biometrics and AI Research Scientist Pasadena, CA- Hybrid Regulatory Compliance Requirements Must have U.S. or Dual Citizenship (with U.S. being one of the citizenships) and be able to obtain post-hire Public Trust Security Clearance from the Department of Homeland Security Position Summary Thales is looking for a Biometrics and AI Research Scientist in our Pasadena, California-based biometric algorithms team who will lead and conduct applied research towards the implementation and improvement of the algorithms underlying our world-class biometric product line. Research areas include biometric image quality assessment, finger friction ridge, face, iris and scars/marks/tattoo recognition, biometric fusion, and presentation attack detection. Key Areas of Responsibility * Develop state-of-the-art biometric algorithms and systems for image quality assessment, recognition, fusion, and presentation attack detection * Evaluate and continuously improve these algorithms for biometric performance, speed, and demographic equitability * Validate each improvement after system integration and for the targeted scenario * Stay abreast of the latest scientific publications in biometrics and pertinent fields of computer vision (CV) * Implement and evaluate published approaches to benchmark them against our own * Propose new approaches for features that differentiate us from the competition * Write near-production level code and practice secure coding standards * Collaborate closely with your team members while effectively using resources within the global organization * Grow into the role of a Thales-wide subject matter expert in your fields of specialization * Prepare submissions for internal and external technology evaluations * Occasionally support pre/post-sales projects * Secure IP by submitting patent applications * Shape research roadmaps in negotiations with product managers and business owners Minimum Qualifications * A Master's of Science with 3+ years of industry in a relevant and technical discipline or a PhD in Electrical Engineering, Computer Science, or a related field * First-authored publications in related conference or journal if you possess a PhD * Prior experience in an analytical role using scientific rigor to create solutions * Collaborative skills with the ability and willingness to strive in a diverse environment * Prior completed-project experience in at least one of the fields: biometrics, 2D or 3D object detection & recognition, pose estimation, segmentation and texture analysis/synthesis * Experience in classical and deep-learning-based machine learning for CV applications, * Background in stochastic signal analysis and detection, as relevant to these fields * A thorough understanding of the digital imaging processing * 3+ years of strong coding skills experience in C/C++ in a corporate setting * Ability to effortlessly switch between the big-picture and detailed view of a problem While not required, an ideal candidate could also have: * Extensive knowledge of deep learning on image processing including convolutional neural network, transformer neural network, graph neural network * Hands-on experience in designing, training, and deploying deep neural networks using PyTorch, Tensorflow, Onnixruntime or OpenVino. * Experience in GPU programming using CUDA or OpenCL * Experience in developing algorithms for fingerprint recognition * Familiarity with concepts of cyber security If you're excited about working with Thales, but not meeting the requirements for this position, we encourage you to join our Talent Community! Special Position Requirements * Occasional domestic or international travel to conferences, trade shows or industry events - approximately 10% Why Join Us? Say HI and learn more about working at Thales click here #LI-Hybrid #LI-RG1 This position will require successfully completing a post-offer background check. Qualified candidates with [a] criminal history will be considered and are not automatically disqualified, consistent with federal law, state law, and local ordinances. We are an equal opportunity employer, including disability and veteran status. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need an accommodation or assistance in order to apply for a position with Thales, please contact us at ************************************. The reference Total Target Compensation (TTC) market range for this position, inclusive of annual base salary and the variable compensation target, is between Total Target Cash (TTC) 130,334.06 - 217,223.44 USD Annual This reflects how companies in a similar industry and geographic region generally pay for similar jobs. This range helps the Company make pay decisions as one data point among many. Where a position falls within this range is also dependent on other factors including - but not limited to - the employee's career path history, competencies, skills and performance, as well as the company's annual salary budget, the customer's program requirements, and the company's internal equity. Thales may offer additional benefits and other compensation, depending on circumstances not related to an applicant's status protected by local, state, or federal law. (For Internal candidate, if you need more information, please reach out to your HR Shared Service, 1st Point) Thales provides an extensive benefits program for all full-time employees working 30 or more hours per week and their eligible dependents, including the following: * Elective Health, Dental, Vision, FSA/HSA, Voluntary Life and AD&D, Whole Group Life w/LTC, Critical Illness, Hospital Indemnity, Accident Insurance, Legal Plan, Identity Theft, and Pet Insurance * Retirement Savings Plan after 30 days of employment with a company contribution and a match, and with no vesting period * Company paid holidays and Paid Time Off * Company provided Life Insurance, AD&D, Disability, Employee Assistance Plan, and Well-being Program

Core Laboratories is the Reservoir Optimization Company™ Core Laboratories Inc. is a leading provider of proprietary and patented reservoir description and production enhancement services and products used to optimize petroleum reservoir performance. The Company has over 70 offices in more than 50 countries and is located in every major oil-producing province in the world. We are well-positioned to serve the growing needs of the energy transition while continuing to fulfill the demand for reliable and affordable energy sources like crude oil and natural gas. Our services, products, expertise, and innovations will continue to be essential as our clients meet the growing demand for energy globally. For more information, visit *********************** At Core Lab, our values matter: Safety, Honesty and Integrity, Customer Focus, Building Trust, and Employee Development. We regard our employees as our greatest asset. We believe that identifying, attracting, developing, and retaining talent are significant actions because our people are so important. SUMMARY We are seeking a highly skilled and detail oriented R&D Scientist with a strong background in analytical chemistry to join our Research & Development team. The ideal candidate will have a strong background in analytical chemistry, with hands-on experience in advanced instrumentation, including GC-MS (single and triple quadrupole), Electron Capture Detector (ECD), Flame Ionization Detector (FID), and HPLC. This role involves method development and supporting the creation of new products and chemical tracers through rigorous experimentation and data analysis. DUTIES & RESPONSIBILITIES Design, plan and execute analytical experiments to support R&D initiatives. Develop, validate, and optimize methods using technics such as Agilent GC-MS (single and triple quadrupole), ECD, FID, and other analytical tools. Analyze and interpret experimental data to draw meaningful conclusions and guide project direction. Maintain, calibrate, and troubleshoot analytical instruments to ensure optimal performance. Collaborate with cross-functional teams including analytical scientists, engineers, and laboratory technicians. Document experimental procedures, results, and conclusions in technical reports and laboratory notebooks. Ensure compliance with laboratory safety protocols, regulatory standards and good laboratory practices (GLP). Contribute to the development, scale-up, and market launch of innovative chemical products and tracer technologies. Stay up to date with scientific publications and technological advancements in analytical and R&D chemistry to inform research strategies and support ongoing development efforts. Develop the vision for the future of Tracer Lab and its technologies. QUALIFICATIONS Master's degree in Chemistry, Analytical Chemistry, or a related field required. 7+ years of experience in an analytical or R&D laboratory setting. Proficiency in Agilent GC-MS (single and triple quadrupole), ECD, FID, HPLC, UV-vis, NMR and related techniques. Experience with data analysis software (e.g., ChemStation, MassHunter). Experience in tracer chemical development, gas analysis or environmental analysis preferred. Familiarity with LIMS, statistical analysis tools and regulatory requirements (e.g., EPA, OSHA, REACH). Project management experience in R&D environments. KNOWLEDGE, SKILLS & ATTRIBUTES Excellent problem-solving skills and attention to detail. Strong written and verbal communication skills. Strong understanding of chemical principles, method development, and validation practices. Ability to work independently and as part of a collaborative team. Knowledge of regulatory requirements for chemical testing and reporting. Core Laboratories, including all of its affiliated and related entities, is an equal opportunity employer and is committed to creating an inclusive environment for everyone. Employment decisions are made regardless of characteristics including, but not limited to, race, color, sex, sexual orientation, gender identity, national origin, age, disability, religion, genetic information, protected veteran or uniformed service member status, and any other characteristic protected under applicable law.

About Us Sino Biological is an internationally recognized reagent supplier and contract research organization, listed on ChiNext of the Shenzhen stock exchange (301047 Sino Biological Inc.). Sino Biological's core technology platform is its in-house developed mammalian cell-based recombinant expression system, which employs proprietary reagents and processes for the efficient production of antigens and antibodies. With its main manufacturing facilities in Beijing, China, Sino Biological also has a growing global presence with a US headquarters in the greater Philadelphia area, a bioprocessing facility in Houston, Texas, and subsidiaries in Frankfurt, Germany, and Tokyo, Japan. As part of its major global expansion, the company has established the Center for Bioprocessing (C4B) in Houston, Texas, located in the world-renowned Texas Medical Center at Levit Green. This vibrant hub is home to some of the most cutting-edge innovation in biotechnology, offering our team an inspiring environment to do meaningful, impactful work in the heart of the medical and research community. Job Description We are seeking an accomplished scientist with industrial experience in recombinant protein and antibody production to join our team as a Senior or Principal R&D Scientist. This role requires strong expertise in sequence and construct design, expression, purification, and characterization of complex biomolecules, including engineered antibody formats (full-length IgG, bispecific, Fab, sc Fv, Fc-fusions) and fusion proteins. The successful candidate will lead small - to medium - scale production projects, serve as a technical authority in molecular and biochemical design, and ensure delivery of high- quality proteins for research and therapeutic applications. While the emphasis is on project leadership, planning, and mentorship, this position also involves hands-on bench work when needed to support critical projects or troubleshooting. Flexibility is required, including potential weekend work and early or late weekday shifts based on project demands. Responsibilities Lead end-to-end protein production projects, from amino acid sequence design to purified, quality-tested product. Design and optimize molecular constructs for recombinant proteins, including antibodies and antibody-derived formats (full-length IgG, bispecific, Fab, sc Fv, Fc-fusions) as well as Fc- and non-Fc fusion proteins. Develop and lead critical SOPs, especially those related to sequence/construct design and molecular engineering, in coordination with upstream, downstream, and analytical teams. Assist with customized project inquiry review. Determine feasibility of protein expressions, identify areas for optimization, and draft production proposals for project managers. Advise and review upstream expression workflows in mammalian and insect systems (HEK293, CHO, Sf9), ensuring reproducibility and scalability. Lead downstream purification strategies using modern chromatography platforms (affinity, IEX, SEC) and contribute to process optimization. Develop and interpret analytical assays, including ELISA, BLI, DSF, HPLC-SEC, and related QC methods, to assess protein quality, stability, and activity. Mentor and supervise associates and junior scientists, ensuring rigorous documentation, data integrity, and efficient lab execution. Collaborate across departments to align on construct design principles, process strategies, and project execution. Perform bench work when necessary to support critical experiments, troubleshooting, or method development. Requirements Ph.D. in Biochemistry, Molecular Biology, Biotechnology, or related field, with 5+ years of industrial experience in recombinant protein and antibody production. Proven expertise in amino acid sequence design and molecular construct development for recombinant proteins, including antibodies (full-length IgG, bispecific, Fab, sc Fv) and fusion proteins (Fc- and non-Fc). Experience with protein structural and sequence analysis software. Demonstrated ability to act as a sole technical contributor and project owner. Hands-on experience with mammalian and insect cell expression systems, as well as chromatography purification (e.g., Cytiva AKTA). Proficiency in protein characterization assays such as ELISA, BLI, DSF, HPLC-SEC, and SDS-PAGE. Strong record of SOP authorship and cross-team collaboration on technical standards. Excellent project management, organizational, and communication skills. Industrial CRO/CMO experience preferred. Flexibility to work occasional early/late shifts or weekends based on project needs. Must be able to lift and move 25-50 lbs as needed. At this time, we are unable to provide visa sponsorship. Applicants must be legally authorized to work in the United States now and in the future without the need for sponsorship. Why Join Us at C4B? Working at Sino Biological's C4B facility isn't just another lab job - it's a chance to be part of something bigger. Here are just a few of the unique benefits of our Houston site: World-class location: Be part of the Texas Medical Center, the largest medical complex in the world, where biotech innovation thrives. Beautiful work environment: Enjoy a brand-new, state-of-the-art facility designed for collaboration and scientific excellence. Free onsite parking: Skip the hassle and expense of parking in the Medical Center - we've got you covered. Free onsite gym: Stay active and energized with convenient access to fitness facilities right at work. Career growth opportunities: Learn directly from industry professionals while growing your career at a global biotech company. Supportive team culture: A welcoming, team-first workplace that values diversity, collaboration, and professional development. Note: Only shortlisted candidates will be contacted for interviews. If selected, an HR team member will reach out to schedule a quick phone interview using the contact information provided in your resume. Sino Biological Inc. is an equal-opportunity employer. We celebrate diversity and are committed to building an inclusive environment for all employees. #LI-Onsite

Job Description We are seeking a highly motivated and experienced R&D Scientist to join our dynamic, fast-paced team focused on driving innovation in the genomic diagnostics field. The R&D Scientist will play a critical role in developing new sequencing based diagnostic assays. This role is ideal for a scientist with a Ph.D. in molecular biology, biochemistry, genetics, or a related field, and a strong background in assay development and validation. The successful candidate will play a key role in developing and optimizing tissue biopsy and liquid biopsy workflows, contributing to the advancement of cutting-edge molecular diagnostic assays. The candidate will independently lead assay development projects while collaborating with cross-functional teams, both within and outside the department, under general supervision. REQUIRED QUALIFICATIONS: Ph.D. in molecular biology, biochemistry, genetics, or related discipline. Minimum of 3 years of hands-on experience in sequencing workflow and assay development, preferably in an industrial or clinical diagnostic setting. Proven expertise in tissue FFPE, fine needle biopsy, and/or cf DNA sequencing workflows. Strong understanding of molecular assay development and validation principles. Proficiency in molecular biology techniques such as PCR, qPCR, NGS, and nucleic acid extraction. Experience with data analysis tools and software relevant to NGS. Excellent problem-solving skills and attention to detail. Strong communication and collaboration skills. PREFERRED QUALIFICATIONS: Agility in learning new concepts and skills and applying them to R&D work. Experience in R&D assay transfer to operation. Experience working in a regulated environment (e.g., CLIA, CAP). Familiarity with automation platforms and liquid handling systems. DUTIES AND RESPONSIBILITIES: Lead and contribute to the design, development, and optimization of molecular assays, with a focus on tissue and cf DNA workflows. Develop DNA library preparation chemistry and workflow for FFPE tissue samples. Refine chemistry and workflows for cell-free DNA library preparation. Design and execute experiments, analyze data, and interpret results to support assay performance and troubleshooting. Define assay performance metrics and collaborate with the validation team on designing verification & validation study. Collaborate cross-functionally with bioinformatics, validation, automation, and clinical teams to ensure robust assay development, validation and transfer. Maintain detailed records of experimental procedures, results, and protocols in accordance with regulatory and quality standards. Present findings and updates to internal stakeholders and contribute to technical reports and publications. Keep up to date with emerging technology and scientific trends, and contribute to new assay improvement or development ideas. Evaluate assay improvement and novel ideas through experimental approach. Adhere to the Code of Conduct as outlined in the Baylor Genetics Compliance Program. Perform other job-related duties as assigned PHYSICAL DEMANDS AND WORK ENVIRONMENT: Frequently required to sit Frequently required to stand Frequently required to utilize hand and finger dexterity Frequently required to talk or hear Frequently required to utilize visual acuity to operate equipment, read technical information, and/or use a keyboard. Occasionally exposed to bloodborne and airborne pathogens or infectious materials EEO Statement: Baylor Genetics is proud to be an equal opportunity employer dedicated to building an inclusive and diverse workforce. We do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, gender identity, veteran status, disability, genetic information, pregnancy, childbirth, or related medical conditions, or any other status protected under applicable federal, state, or local law.

Job Description "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.

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.

We have an exciting opportunity for a Research Scientist I, Analytical Chemist at UL Research Institutes, Electrochemical Safety Research Institute (ESRI) based in our Houston, Texas facilities. The Research Scientist I, Analytical Chemist will under general direction, supports experimental and analytical research through the execution of laboratory experiments, data collection and interpretation, and preparation of technical reports. This role collaborates with senior research scientists and engineers to ensure all procedures and results meet rigorous scientific standards. Responsibilities also include the routine operation, calibration, and maintenance of analytical instruments to support daily laboratory functions. UL Research Institutes: At UL Research Institutes (ULRI), we expand the boundaries of safety science to create a more secure and sustainable world. For more than a century, we have studied the unintended consequences of innovation, designed solutions to mitigate risk and shared our findings with academia, scientists, manufacturers, and policymakers across industries. We identify critical safety and sustainability issues, asking the tough questions because we believe a safer world begins with knowledge. Build a safer, more secure, and sustainable future with us. Join us and work with our Electrochemical Safety Research Institute team who conduct the research required to produce that knowledge and put into practice. Electrochemical Safety Research Institute: The Electrochemical Safety Research Institute investigates the safety and performance limits of energy technologies. Through our discovery-driven research, we innovate, test, model, and lay the foundation for electrochemical energy storage that is both safe and reliable. Our scientific research helps everyone in the energy storage and battery value chain - from cell and battery manufacturers, suppliers, and original equipment manufacturers to recyclers, shippers, and consumers - understand and thereby help minimize the various safety risks associated with batteries in various applications, including electric vehicles and renewable energy storage systems. Collaborating with a wide variety of partners to help meet the world's energy safety needs, we disseminate information by convening a diverse group of stakeholders at events such as global battery summits and webinars to find data-driven solutions to new and emerging energy storage risks. What you'll learn and achieve: As the Research Scientist I, you will play a key role in the rapid growth of UL as you: Identify fundamental knowledge needed to enhance UL's thought leadership and support the strategy of UL. Document laboratory procedures and prepare detailed reports that include data plotting and analysis. Evaluate technical specifications and factors related to process or design objectives using a variety of analytical techniques, including Gas Chromatography-Mass Spectrometry (GC-MS), X-Ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), Thermogravimetric Analysis/Differential Scanning Calorimetry (TGA/DSC), Ultraviolet-Visible (UV/Vis) Spectroscopy, and Accelerating Rate Calorimetry (ARC). Identify and recommend appropriate hardware and equipment necessary for analytical operations. Remain current on emerging technologies and scientific trends by engaging with scientific literature and attending academic conferences. Support project initiation by gathering preliminary data and collaborating with research engineers and scientists to execute experiments. Develop and refine analytical methods and data analysis procedures to improve lab efficiency and data accuracy. What you'll experience working at UL Research Institutes: We have pursued our mission of working for a safer, more secure, and sustainable world for over 130 years, embedding conscientious stewardship into everything we do. People: Our people make us special. You'll work with a diverse team of experts respected for their independence and transparency and build a network, because our approach is collaborative. We collaborate across disciplines, organizations, and geographies to build the global scientific response that today's global challenges require. Interesting work: Every day is different for us here. We see what's on the horizon and use our expertise to build the foundations of a safer future. You'll have the opportunity to push the boundaries of human understanding as part of a team working to advance the public good. Grow and achieve: We learn, work, and grow together through targeted development, reward, and recognition programs. Values. Four core values guide our work: collaboration, respect, integrity, and beneficence. By living our values, we inspire the trust essential to fulfilling our mission and foster the partnerships that enable us to pursue a beneficent future in which we all can thrive. Total Rewards: All employees at UL Research Institutes are eligible for bonus compensation. We offer comprehensive medical, dental, vision, and life insurance plans and a generous 401k matching structure of up to 5% of eligible pay. Moreover, we invest an additional 4% into your retirement saving fund after your first year of continuous employment. Depending on your role, you may be able to discuss flexible working arrangements with your manager. We also provide employees with paid time off, including vacation, holiday, sick, and volunteer days. Perform other duties as assigned. What makes you a great fit: While no one candidate will embody every quality, the successful candidate will bring many of the following professional competencies and personal attributes: Demonstrated ability to maintain academic and applied knowledge and skills. Demonstrated knowledge of data collection, analysis and plotting, ability to take videos and photos as necessary during the tests. Demonstrated knowledge of handling analytical instruments such as FTIR, GC-MS, SEM-EDX, TGA-DSC, XRD, etc. in a chemistry lab. Excellent problem-solving skills related to instrumentation and data interpretation. Excellent communication skills both written and verbal. Ability to collaborate with peers and work directly with research scientists and other team members to complete a project from start to finish. Professional education and experience requirements for the role include: Bachelor's degree or higher in Chemistry, Materials Science, or Chemical Engineering Minimum 2 years of directly related work experience About UL Research Institutes and UL Standards & Engagement UL Research Institutes and UL Standards & Engagement are nonprofit organizations dedicated to advancing safety science research through the discovery and application of scientific knowledge. We conduct rigorous independent research and analyze safety data, convene experts worldwide to address risks, share knowledge through safety education and public outreach initiatives, and develop standards to guide safe commercialization of evolving technologies. We foster communities of safety, from grassroots initiatives for neighborhoods to summits of world leaders. Our organization employs collaborative and scientific approaches with partners and stakeholders to drive innovation and progress toward improving safety, security, and sustainability, ultimately enhancing societal well-being. Our affiliate, UL Solutions, stands alongside us in working for a safer and more sustainable world. UL Solutions conducts testing, verification and certification, and provides training and advisory services, along with data-driven reporting and decision-making tools, for customers around the world. To learn more, visit our websites UL.org and ULSE.org. Salary Range: $61,199.38-$84,149.14 Pay Type: Salary

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.

Sr. Med Lab Scientist, LabServ - Hematology (Days) - (2506382) Description JOB SUMMARY:Senior Medical Laboratory Scientist, Laboratory Services provides administrative and technical skills necessary to organize, supervise, and complete various medical laboratory procedures within a section. REQUIRED EDUCATION / EXPERIENCE:Bachelor's degree in a Clinical Laboratory Science or Basic Science with two (2) years related experience. Technologist level certification from either the American Society of Clinical Pathology (ASCP), American Board of Medical Technology (AMT), or the American Board of Histocompatibility and Immunogenetics (ABHI) or equivalent certification. Qualifies as Testing Personnel for high complexity testing under the Clinical Laboratory Improvement Amendment (CLIA). Preferred:Specialty certification and clinical laboratory hematology experience. ESSENTIAL JOB FUNCTIONS:• Responsible for recruitment, hiring, payroll, orientation, training, supervision, evaluation, competency assessment, coaching, disciplinary action and/or termination process of divisional employees. • Supervises the work of laboratory personnel engaged in performing routine and specialized technical procedures, including planning laboratory work, evaluating work performed and handling procedural and technical laboratory problems. • Acts as lead worker, supervises, directs, plans, develops, implements, evaluates, and oversees the execution of daily operations including scheduling work assignments. • Assists section leadership in developing protocols and procedures for the area, and reviews and updates existing procedures. • Responsible for ensuring that the laboratory division functions with the appropriate level of staff to guarantee an efficient operation. • Reviews and evaluates accuracy of lab data and reports patient results with all required documentation. • Assists personnel with complex procedures, exercising independent judgment and responsibility. • Ability to work independently within established guidelines, apply problem-solving skills, meet deadlines and meet urgent patient, provider, and system needs. • Assists with Quality Management activities including but not limited to evaluating quality of reported test results, quality control and equipment maintenance procedures, proficiency testing and verifying appropriate documentation is maintained and corrective actions are implemented as necessary. • Assists in evaluations of new tests or instruments, as assigned. • Maintains inventory of reagents and other supplies including ordering supplies and monitoring expenditures and providing input for budget. • Communicates pertinent information to staff members, management, medical directors, and other divisions. • Serves as a liaison between departmental staff, management, and supervisory staff. • Performs laboratory testing as required per division. • Instructs and trains students. • Available to cover different shifts if requested to guarantee patient care. • Responsible for maintaining compliance with regulatory accreditation standards. • Adheres to internal controls and reporting structure. • Adheres to all safety protocols in each laboratory area. WORK SCHEDULE:Day shift 6:30am to 3:00pm, Monday - Friday, rotating weekends and holidays. Qualifications Equal Employment OpportunityUTMB 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: 0419 Clinical Services Wing 301 University Blvd. Galveston 77555-0419Job: Clinical LaboratoryOrganization: UTMB Health: RegularShift: StandardEmployee Status: SupervisorJob Level: Day ShiftJob Posting: Nov 11, 2025, 8:44:51 PM

The Museum of Fine Arts, Houston (MFAH) seeks an Assistant/Associate/ Conservation Scientist to join a collaborative, cross-disciplinary team committed to the care, interpretation, and study of the museum's diverse collection. This is a full-time position housed within the Conservation Department, where science is integrated into broader museum practice with a strong emphasis on curiosity, transparency, and shared responsibility. The Assistant/Associate/ Conservation Scientist supports ongoing conservation treatments, acquisitions, and research projects through advanced scientific analysis, interpretive insight, and clear communication. Working alongside conservators, curators, collections staff, and educators, the scientist will contribute meaningfully to the understanding and preservation of works of art across cultures, time periods, and media. What We're Looking For We're seeking someone who: Is scientifically grounded, with expertise in conservation science, chemistry, or a related field, and values interpretation and context in a museum setting. Works collaboratively. This is a team-driven lab rooted in generosity of knowledge, time, and credit. Thrives in complexity, comfortably navigating both the analytical and passionate nuances of museum work. Sees conservation as a shared responsibility, working effectively across disciplines and job titles. Leads with humility and curiosity, fostering a culture of learning and mutual respect. Is values-driven, with integrity, empathy, and a respect for diverse lived experiences at the core of their approach. Understands that how we work matters-and that excellence should never come at the cost of well-being, equity, or kindness. Primary Responsibilities Design and conduct non-destructive and micro-destructive analysis using a range of techniques (e.g., SEM-EDS, XRF, FTIR, Raman spectroscopy, GC-MS, PLM). Collaborate with curators and conservators to determine analytical priorities, develop methodologies, and interpret results within historical and material contexts. Manage daily lab operations including workflow, documentation, equipment care, and inventory within budget. Generate technical reports, contribute to peer-reviewed publications, and present research at professional conferences. Maintain digital records and ensure proper archiving of data, images, samples, and reports. Supervise and mentor interns, fellows, or visiting researchers as applicable. Support educational and outreach efforts, including talks, tours, and public programming. Advise on preventive conservation strategies, environmental monitoring, and materials evaluation. Participate in departmental planning, professional development, and institutional initiatives including emergency preparedness and strategic projects. Minimum Qualifications Ph.D. in chemistry, physics, materials science, or a closely related field. Minimum five years of applied scientific research experience in cultural heritage, preferably in a museum setting. Demonstrated knowledge of materials used in works of art, degradation mechanisms, and conservation techniques. Advanced instrumental skills in analytical methods commonly used in heritage science. A record of peer-reviewed publications or public scholarship in conservation science or related disciplines. Excellent interpersonal and communication skills, with the ability to collaborate across departments and share knowledge with both technical and non-technical audiences. Strong organizational, computational, and data management skills. Legal eligibility to work in the United States. Work Environment & Physical Demands Ability to occasionally lift up to 50 pounds; manual dexterity required for handling delicate objects and instruments. Activities include standing, walking, sitting, bending, kneeling, and climbing. Use of PPE as needed for chemical and analytical processes. The MFAH is equally committed to the full inclusion of all qualified individuals interested in employment with the organization. As part of this commitment, we want to ensure that persons with disabilities are provided reasonable accommodation needed to 1) participate in the job application or 2) interview process; 3) perform essential job functions; and/or 4) participate in the benefits and privileges of employment with the MFAH. If reasonable accommodation is needed, please contact the human resources department: *********** Compensation and Benefits Benefits The Museum of Fine Arts, Houston, offers an excellent benefits package that includes: Medical Insurance : Employee and dependent coverage through a choice of managed health care programs Dental Insurance : Employee and dependent coverage through two plan choices Vision Insurance : Employee and dependent coverage through a vision program Group health, dental and vision insurance coverage available and effective the first of the month following employment with the MFAH for this role. Life Insurance & AD&D : Employee coverage at no cost to the employee Long Term Disability : Employee coverage at no cost to the employee The MFAH provides a generous schedule for time off under the following benefit categories: Paid Time Off - Used for absences from work such as vacation, illness of short duration, and personal reasons. Hours are accrued biweekly, based on employment status, length of service, and hours worked Reserve Time Off - Used for extended illnesses. Employees accrue up to 6 days per year, up to a maximum of 120 days Holidays - Full-time employees receive eleven paid holidays per year Volunteer Time Off - The MFAH supports activities that enhance and serve the communities in which we live and work. Employees receive up to 40 hours of paid time off annually to give back and volunteer. Other Benefits Staff may contribute to the MFAH Retirement Savings Plan. Eligible staff contributing to the plan may receive up to a 5% matching contribution from the MFAH after one year of service. ( We also recognize prior nonprofit service which will provide for an accelerated employer match! ) Roth IRA also available! MFAH Membership - Staff receive a free Family-level membership Discounts - Staff receive discounts on purchases at the Museum shop and all on campus eateries and courses for you or your family at the Glassell School of Art. Metro commuter subsidy available upon request Professional development support and museum membership Relocation assistance and research-related travel funds may be available Compensation Salary will be commensurate with the applicant's experience and the needs and requirements expressed in the . The MFAH has set the pay range for this job and level as a general guideline and not a guarantee of the compensation amount or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, the needs and requirements expressed in the , as well as internal equity, and alignment with market data, and any related regulations or other laws. How to Apply Qualified applicants should apply online, which will be the most effective way to ensure consideration. Application materials should include: CV or résumé Cover letter addressing your qualifications, interest in the position, and how your values align with the MFAH's mission Contact information for three professional references Applications or letters of interest sent via mail, fax, or direct email to a staff member will not ensure consideration. Visit the MFAH Careers page at - *********************************** "Click" on All current employment opportunities Scroll through the listings to find this role. "Click" and apply! It's that easy. About the MFAH Conservation Environment The Sarah Campbell Blaffer Foundation Center for Conservation at the Museum of Fine Arts, Houston, is home to 21 diverse and highly skilled team of conservation professionals dedicated to the preservation and study of the museum's encyclopedic collection. The staff includes specialists in paintings, paper, photo, science, sculpture and objects, textiles, time-based media art, as well as imaging specialist, conservation technicians, matting and framing technicians, fellows, and interns. We care for an encyclopedic collection, which includes almost 80,000 objects and spans 5,000 years of achievement in the arts. Together, we bring a wide range of expertise in historical and contemporary materials, treatment methodologies, and preventive conservation. We have a collaborative spirit, with intellectual rigor, and commitment to ethical and inclusive practice, our team works closely with curators, educators, and scientists to advance cross-disciplinary research, public engagement, and innovative approaches to collections care. The Center fosters a supportive environment where mentorship, transparency, and continual learning are core values. We are proud to be one of the most diverse conservation laboratories in the U.S.-and we approach that responsibility with care, respect, and determination. The MFAH is an organization comprised of 600+ employees and 1,000+ docents and volunteers. The museum is more than 100 years old and ranks nationally among the top 10 art museums in exhibition space, memberships, endowments, and attendance, with 1M visitors annually. Our multifaceted institution includes multiple gallery buildings, a sculpture garden, two art schools, three eateries and two house museums for decorative arts. The encyclopedic collection numbers more than 70,000 works of art in a wide range of media. As an employer, MFAH offers a supportive, collegial and inclusive work environment and a competitive benefits package. Working Conditions and Physical Demands Work will primarily be performed in an office environment. Work will involve extended sitting and computer use. With or without reasonable accommodation, the individual selected must have the capacity to perform effectively all essential functions. In addition to the other demands mentioned, the demands of the job may or will include: Must undergo and meet company standards for background and reference checks. Required ability to handle multiple tasks concurrently. Extensive computer usage. Seeing, hearing, speaking, and writing clearly in order to communicate with staff, guests and others. Frequent sitting, standing, bending, kneeling, climbing, and walking, which may be required for extended periods of time. Good vision or corrected by use of glasses and/or contacts for reading and viewing abilities. Ability to occasionally lift up to 50 pounds; manual dexterity required for handling delicate objects and instruments. Use of PPE as needed for chemical and analytical processes. Equal Opportunities for All At the MFAH, we believe that diversity, equity, accessibility, and inclusivity are fundamental to our organization. We welcome all candidates whose experience has prepared them to contribute to our organization and our pledge for workplace diversity, inclusion, and excellence. Our commitment to our policy and practice of nondiscrimination represents more than good intentions. It provides for employment decisions that are made without regard to race, creed, color, age, gender, sexual orientation, religion, national origin, gender identity or expression, genetic information, disability, or veteran status, or any other protected characteristic as established by law or any other reason unrelated to your ability to join and contribute to our organization and support our mission to provide a museum experience for all. Research shows some individuals from underrepresented backgrounds often apply to jobs only if they meet 100% of the qualifications. We recognize that it is highly unlikely that an applicant meets 100% of the qualifications for a given role. Therefore, if much of this job description describes you, then you are highly encouraged to apply for this role. The MFAH is equally committed to the full inclusion of all qualified individuals interested in employment with the organization. As part of this commitment, we want to ensure that persons with disabilities are provided reasonable accommodation needed to 1) participate in the job application or 2) interview process; 3) perform essential job functions; and/or 4) participate in the benefits and privileges of employment with the MFAH. If reasonable accommodation is needed, please contact the human resources department: ***********

Amentum is actively seeking applicants for Associate Scientist 1 Houston, TX Amentum Position Description: The Associate Scientist 1 - shall perform, at a minimum, the following tasks and responsibilities in accordance with standard operating procedures: Must be able to obtain/maintain a DHS Suitability security clearance * Handling, receipt, and processing of operational, Quality Assurance (QA), and proficiency test (PT) samples potentially containing biological threat agents * Performing non-research biological science work utilizing microbiological and molecular techniques, including, but not limited to, DNA extraction and real-time polymerase chain reaction (real-time PCR) to identify and characterize pathogenic bacterial and viral agents * Preparing reagents and samples * Familiarity with Good Laboratory Practice (GLP) * Decontamination of work spaces, including Biological Safety Cabinets (BSCs), hoods/air boxes, equipment, and other items associated with processing and analysis activities * Maintaining chain-of-custody * Interpretation of results * Data entry utilizing computerized or computer-linked systems * Performing routine equipment calibration, cleaning, assembly, and maintenance * Collecting, processing, and analyzing internal laboratory swipes/swabs for Quality Assurance/Quality Control (QA/QC) and contamination monitoring * Proper disposal of biohazardous waste * Restocking and maintaining proper inventory of necessary supplies * Supporting Program logistics in conducting and documenting annual inventory of DHS-procured durable equipment and property * QA/QC and acceptance testing of reagents in accordance with applicable Standard Operating Procedures (SOPs) and the Laboratory Operations Quality Assurance Program Plan (QAPP) * Adhering to QA/QC requirements in accordance with the Public Health Laboratory quality management systems and the QAPP * Maintaining documentation of records demonstrating compliance with applicable training/retraining, competencies, and document reviews * Analyzing routine external QA samples in accordance with the SOP's and QA Program guidance * Proper archiving, storage, and shipping of samples * Demonstrating ability to follow and adhere to written procedures and accepted practices in accordance with federal, state, and local regulations, safety, security and dress code policies, procedures, and guidelines, including DHS Safeguarding Sensitive but Unclassified (For Official Use Only) Information (January 2005) when visiting or working at Government facilities * Preparing written and oral technical reports, answering questions, and making recommendations to the Lead Biological Scientist for inclusion in comprehensive reports * Accurately performing work with confidence * Demonstrating competency in various testing methodologies (e.g., multi-center studies), evaluating potential products and processes against unique environmental backgrounds, and meeting established deadlines * Scheduled workdays include weekends and holidays * Must be present for all hours of the workday, and be available 24/7/365 in case of emergency Position Minimum Requirements/Qualifications: * minimum of a Bachelor's degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences, and at least one (1) year of laboratory bench experience outside of an academic environment, utilizing PCR, aseptic techniques, and biological assays. * Biological Safety Level (BSL)-3 experience is desirable. Amentum is proud to be an Equal Opportunity Employer. Our hiring practices provide equal opportunity for employment without regard to race, sex, sexual orientation, pregnancy (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, ancestry, United States military or veteran status, color, religion, creed, marital or domestic partner status, medical condition, genetic information, national origin, citizenship status, low-income status, or mental or physical disability so long as the essential functions of the job can be performed with or without reasonable accommodation, or any other protected category under federal, state, or local law. Learn more about your rights under Federal laws and supplemental language at Labor Laws Posters.

Our client is looking for an Application Scientist to provide technical assistance to Crop Solutions' customers to sustain the current businesses and with the objective of developing new business at these customers. Main responsibilities include: Ensure products meet the client's exact standards (internal and external). Conducts research and directs lab work for such purposes as product/application development, etc. Devises and develops ways and methods for the solution of technical problems. Possesses a full understanding of the uses and applications of existing products and related product lines. Develops new product concepts including proprietary blends using both products and co-producer products. Compiles applications information specific to the product line and interfaces with internal and external customers to solve specific product needs. Lead product and process developments for the crop protection, agrochemical, and related markets. Education, Experience and Skills Required Degree in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry/Engineering. Minimum 5 years of experience in Agrochemical formulations: pesticides functions / active ingredients/types of formulations / experimental methodologies /regulatory framework in Ag/agronomy required Surfactants experience R&D experience Technical + Commercial profile

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 AG seeks an outstanding Process Validation Scientist III to uphold high standards in MSAT SS. Lead PPQ, APS, and CPV for Viral Vector and Cell Therapy in Houston, TX. Key Responsibilities: The PV Scientist III is responsible for the planning, execution, and close-out of PPQ, APS, and CPV activities for Viral Vector and Cell Therapy processes. Ensure timely and in-full delivery of tasks, activities, and documents Generate PPQ/PV/APS/CPV reports as required Lead projects involving PPQ/APS/CPV activities and communicate with Quality Control, Quality Assurance, Supply Chain/ERP, Manufacturing, Data Science, and the Commercial Development Organization Work with other MSAT teams on complex problems requiring diverse scope analysis Key Qualifications: Bachelor's Degree in Science or related field 5 years of relevant experience Experience in Viral Vectors/Cell Therapy/Biologics PPQ/PV/APS/CPV, Technology Transfer, MSAT, and/or Manufacturing preferred Proven ability to challenge the status quo and seek improvements Embrace and drive new initiatives successfully Effective engagement in change processes Understand and explain corporate strategy to peers and team Provide feedback on strategy content and implementation Actively seek and share diverse perspectives Champion and role model diversity and inclusion values Proactively understand customer and market needs Develop insights to improve customer happiness Develop resource plans and prioritize demands Ensure delivery excellence for personal and team goals Regularly solicit and address feedback Establish a positive work environment while demonstrating high integrity Lonza AG is dedicated to encouraging an inclusive and collaborative work environment, where every team member's contribution is valued and respected. Compensation for the role will depend on a number of factors, including the successful candidate's qualifications, skills, competencies, experience, and job-related knowledge. Full-time employees receive a comprehensive benefits package including performance-related bonus, medical and dental coverage, 401k plan, life insurance, short-term and long-term disability insurance, an employee assistance program, paid time off (PTO), and more. 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.

Higher education requirements include: Completing a bachelor's degree in medical technology or clinical laboratory science. A bachelor's degree in a science or health related field (e.g. chemistry or microbiology) may also be considered. Completing a clinical laboratory program or internship through a hospital-based program or as part of their education National certification as a medical technologist (MT), clinical laboratory scientist (CLS), or medical laboratory scientist (MLS) Previous experience in a health care setting Responsibilities and duties, including: Examining and analyzing blood, body fluids, tissues, and cells Relaying test results to physicians Utilizing microscopes, cell counters, and other high-precision lab equipment Cross matching blood for transfusion Monitoring patient outcomes Performing differential cell counts looking for abnormal cells to aid in the diagnosis of anemia and leukemia Establishing quality assurance programs to monitor and ensure the accuracy of test results Overseeing the work of a medical laboratory technician

Job Description Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood! You won't find a work culture and benefits package like ours every day. Come join our team and a group of colleagues who love working at Castle! Learn more at ************************* Castle Biosciences Inc. is growing, and we are looking to hire a full-time R&D, Senior Scientist working from our Friendswood, TX office location, with a start date of February 1, 2026. Why Castle Biosciences? Exceptional Benefits Package: Excellent Annual Salary + 20% Bonus Potential 20 Accrued PTO Days Annually + 10 Paid Holidays 401K with 100% Company Match up to 6% 3 Health Care Plan Options + Company HSA Contribution Company Stock Grant Upon Hire A DAY IN THE LIFE OF A Senior Scientist The Senior Scientist will work with R&D colleagues to develop evidence to support launched products in dermatology, while also collaborating across Castle Biosciences to produce key scientific materials such as publications, abstracts, slide decks, and other literature for internal training and external education. This role will spend the most time on data analysis, data presentation, collaboration with Marketing, Sales, and Medical Affairs, as well as publication planning, writing, and editing. REQUIREMENTS PhD level training in life sciences Experience related to Atopic Dermatitis preferred The ability to successfully communicate and teach in a complex and competitive environment. Strong interpersonal, organizational, and communication skills, written and oral. Demonstrated team player. SCHEDULE Monday - Friday, in-office 5 days a week from 9:00 am to 5:30 pm, exempt position, working from the Friendswood, TX office. Off-hour work will be required to facilitate communication and meet deadlines. READY TO JOIN OUR BIOTECH TEAM? We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon! Castle Biosciences Awards and Research Developments! WORK AUTHORIZATION All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas. ABOUT CASTLE BIOSCIENCES INC. At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes. Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development. Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail ReasonableAccommodationsRequest@castlebiosciences.com. This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. ** No third-party recruiters, please Job Posted by ApplicantPro

Location: Pasadena, United States of AmericaThales people architect identity management and data protection solutions at the heart of digital security. Business and governments rely on us to bring trust to the billons of digital interactions they have with people. Our technologies and services help banks exchange funds, people cross borders, energy become smarter and much more. More than 30,000 organizations already rely on us to verify the identities of people and things, grant access to digital services, analyze vast quantities of information and encrypt data to make the connected world more secure. Biometrics and AI Research Scientist Pasadena, CA- Hybrid Regulatory Compliance Requirements Must have U.S. or Dual Citizenship (with U.S. being one of the citizenships) and be able to obtain post-hire Public Trust Security Clearance from the Department of Homeland Security Position Summary Thales is looking for a Biometrics and AI Research Scientist in our Pasadena, California-based biometric algorithms team who will lead and conduct applied research towards the implementation and improvement of the algorithms underlying our world-class biometric product line. Research areas include biometric image quality assessment, finger friction ridge, face, iris and scars/marks/tattoo recognition, biometric fusion, and presentation attack detection. Key Areas of Responsibility Develop state-of-the-art biometric algorithms and systems for image quality assessment, recognition, fusion, and presentation attack detection Evaluate and continuously improve these algorithms for biometric performance, speed, and demographic equitability Validate each improvement after system integration and for the targeted scenario Stay abreast of the latest scientific publications in biometrics and pertinent fields of computer vision (CV) Implement and evaluate published approaches to benchmark them against our own Propose new approaches for features that differentiate us from the competition Write near-production level code and practice secure coding standards Collaborate closely with your team members while effectively using resources within the global organization Grow into the role of a Thales-wide subject matter expert in your fields of specialization Prepare submissions for internal and external technology evaluations Occasionally support pre/post-sales projects Secure IP by submitting patent applications Shape research roadmaps in negotiations with product managers and business owners Minimum Qualifications A Master's of Science with 3+ years of industry in a relevant and technical discipline or a PhD in Electrical Engineering, Computer Science, or a related field First-authored publications in related conference or journal if you possess a PhD Prior experience in an analytical role using scientific rigor to create solutions Collaborative skills with the ability and willingness to strive in a diverse environment Prior completed-project experience in at least one of the fields: biometrics, 2D or 3D object detection & recognition, pose estimation, segmentation and texture analysis/synthesis Experience in classical and deep-learning-based machine learning for CV applications, Background in stochastic signal analysis and detection, as relevant to these fields A thorough understanding of the digital imaging processing 3+ years of strong coding skills experience in C/C++ in a corporate setting Ability to effortlessly switch between the big-picture and detailed view of a problem While not required, an ideal candidate could also have: Extensive knowledge of deep learning on image processing including convolutional neural network, transformer neural network, graph neural network Hands-on experience in designing, training, and deploying deep neural networks using PyTorch, Tensorflow, Onnixruntime or OpenVino. Experience in GPU programming using CUDA or OpenCL Experience in developing algorithms for fingerprint recognition Familiarity with concepts of cyber security If you're excited about working with Thales, but not meeting the requirements for this position, we encourage you to join our Talent Community! Special Position Requirements Occasional domestic or international travel to conferences, trade shows or industry events - approximately 10% Why Join Us? Say HI and learn more about working at Thales click here #LI-Hybrid #LI-RG1 This position will require successfully completing a post-offer background check. Qualified candidates with [a] criminal history will be considered and are not automatically disqualified, consistent with federal law, state law, and local ordinances. We are an equal opportunity employer, including disability and veteran status. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need an accommodation or assistance in order to apply for a position with Thales, please contact us at ************************************. The reference Total Target Compensation (TTC) market range for this position, inclusive of annual base salary and the variable compensation target, is between Total Target Cash (TTC) 130,334.06 - 217,223.44 USD Annual This reflects how companies in a similar industry and geographic region generally pay for similar jobs. This range helps the Company make pay decisions as one data point among many. Where a position falls within this range is also dependent on other factors including - but not limited to - the employee's career path history, competencies, skills and performance, as well as the company's annual salary budget, the customer's program requirements, and the company's internal equity. Thales may offer additional benefits and other compensation, depending on circumstances not related to an applicant's status protected by local, state, or federal law. (For Internal candidate, if you need more information, please reach out to your HR Shared Service, 1st Point) Thales provides an extensive benefits program for all full-time employees working 30 or more hours per week and their eligible dependents, including the following: •Elective Health, Dental, Vision, FSA/HSA, Voluntary Life and AD&D, Whole Group Life w/LTC, Critical Illness, Hospital Indemnity, Accident Insurance, Legal Plan, Identity Theft, and Pet Insurance •Retirement Savings Plan after 30 days of employment with a company contribution and a match, and with no vesting period •Company paid holidays and Paid Time Off •Company provided Life Insurance, AD&D, Disability, Employee Assistance Plan, and Well-being Program

About Us Sino Biological is an internationally recognized reagent supplier and contract research organization, listed on ChiNext of the Shenzhen stock exchange (301047 Sino Biological Inc.). Sino Biological's core technology platform is its in-house developed mammalian cell-based recombinant expression system, which employs proprietary reagents and processes for the efficient production of antigens and antibodies. With its main manufacturing facilities in Beijing, China, Sino Biological also has a growing global presence with a US headquarters in the greater Philadelphia area, a bioprocessing facility in Houston, Texas, and subsidiaries in Frankfurt, Germany, and Tokyo, Japan. As part of its major global expansion, the company has established the Center for Bioprocessing (C4B) in Houston, Texas, located in the renowned Texas Medical Center at Levit Green. C4B is equipped with state-of-the-art facilities and staffed by a team of experts, driving innovation in bioprocessing. Job Title: R&D Scientist Location: Houston, TX Department: Center for Bioprocessing (C4B), Sino Biological US, Inc. Position Type: Full-time Job Description This position is suited for experienced scientists with a strong background in protein purification, characterization, and bioprocess development in an industrial environment. The Scientist or Senior Scientist will play a key role in leading and executing downstream process development, including chromatography-based purification and recombinant protein quality assessment. The role involves independent design and optimization of purification workflows, supervision of junior staff, and collaboration with upstream and operations teams to support internal pipeline and client-based programs. Responsibilities include method development, hands-on operation of FPLC systems (e.g., Cytiva AKTA), and analytical techniques such as HPLC-SEC, ELISA, and DSF to evaluate product quality and process consistency. The successful candidate will demonstrate strong scientific judgment, attention to detail, and the ability to document and communicate results clearly in a fast-paced, team-oriented setting. Flexibility is required, including potential weekend work and early or late weekday shifts based on project demands. Responsibilities * Lead bioprocessing projects and supervise associates in wet lab activities related to recombinant protein and antibody production. * Design and improve upstream and downstream bioprocessing workflows, contribute to project planning, and review project information to provide feedback on recombinant protein and antibody design for upstream and downstream processes. * Develop and optimize assays to evaluate protein interactions, stability, and quality controls, including BLI, ELISA, HPLC-SEC, DSF, and related analytical methods. * Oversee maintenance, calibration, and troubleshooting of bioprocessing instruments. * Collaborate with cross-functional teams to ensure alignment with project goals. * Maintain accurate and organized documentation, including experimental records and technical reports. * Ensure compliance with laboratory safety practices and OSHA guidelines. Requirements * MS or PhD in Biochemistry, Biotechnology, Molecular Biology, or a related field. * Several years of relevant experience in recombinant protein and antibody design, expression, purification, and characterization, as well as novel bioprocess development. * Proficiency in protein characterization assays such as BLI, ELISA, and DSF, and analytical techniques such as HPLC-SEC. * Strong knowledge of mammalian expression systems and downstream purification workflows, including HEK293/CHO expression and Cytiva AKTA or other FPLC platform applications. * Industrial experience is preferred. * Excellent organizational, analytical, and communication skills. * Willingness to work a flexible schedule, including occasional morning, evening, and weekend hours. * Must be able to lift and move 25-50 lbs as needed. Why Join Us? * Competitive compensation package. * Learn directly from industry professionals in a global biotech company. * Career growth opportunities and mentorship. * A welcoming, team-first workplace that celebrates diversity and collaboration. Note: Only shortlisted candidates will be contacted for interviews. If selected, an HR team member will reach out to schedule a quick phone interview using the contact information provided in your resume. Sino Biological Inc. is an equal-opportunity employer. We celebrate diversity and are committed to building an inclusive environment for all employees. #LI-Onsite

**Amentum** is actively seeking applicants for **Associate Scientist 1** ** **Houston, TX** **Amentum Position Description:** The Associate Scientist 1 **-** shall perform **, at a minimum,** the following tasks and responsibilities in accordance with standard operating procedures **:** **Must be able to obtain/maintain a DHS Suitability security clearance** + Handling, receipt, and processing of operational, Quality Assurance (QA), and proficiency test (PT) samples potentially containing biological threat agents + Performing non-research biological science work utilizing microbiological and molecular techniques, including, but not limited to, DNA extraction and real-time polymerase chain reaction (real-time PCR) to identify and characterize pathogenic bacterial and viral agents + Preparing reagents and samples + Familiarity with Good Laboratory Practice (GLP) + Decontamination of work spaces, including Biological Safety Cabinets (BSCs), hoods/air boxes, equipment, and other items associated with processing and analysis activities + Maintaining chain-of-custody + Interpretation of results + Data entry utilizing computerized or computer-linked systems + Performing routine equipment calibration, cleaning, assembly, and maintenance + Collecting, processing, and analyzing internal laboratory swipes/swabs for Quality Assurance/Quality Control (QA/QC) and contamination monitoring + Proper disposal of biohazardous waste + Restocking and maintaining proper inventory of necessary supplies + Supporting Program logistics in conducting and documenting annual inventory of DHS-procured durable equipment and property + QA/QC and acceptance testing of reagents in accordance with applicable Standard Operating Procedures (SOPs) and the Laboratory Operations Quality Assurance Program Plan (QAPP) + Adhering to QA/QC requirements in accordance with the Public Health Laboratory quality management systems and the QAPP + Maintaining documentation of records demonstrating compliance with applicable training/retraining, competencies, and document reviews + Analyzing routine external QA samples in accordance with the SOP's and QA Program guidance + Proper archiving, storage, and shipping of samples + Demonstrating ability to follow and adhere to written procedures and accepted practices in accordance with federal, state, and local regulations, safety, security and dress code policies, procedures, and guidelines, including DHS Safeguarding Sensitive but Unclassified (For Official Use Only) Information (January 2005) when visiting or working at Government facilities + Preparing written and oral technical reports, answering questions, and making recommendations to the Lead Biological Scientist for inclusion in comprehensive reports + Accurately performing work with confidence + Demonstrating competency in various testing methodologies (e.g., multi-center studies), evaluating potential products and processes against unique environmental backgrounds, and meeting established deadlines + Scheduled workdays include weekends and holidays + Must be present for all hours of the workday, and be available 24/7/365 in case of emergency **Position Minimum Requirements/Qualifications:** + minimum of a Bachelor's degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences, and at **least one (1) year** of laboratory bench experience outside of an academic environment, utilizing PCR, aseptic techniques, and biological assays. + Biological Safety Level (BSL)-3 experience is desirable. Amentum is proud to be an Equal Opportunity Employer. Our hiring practices provide equal opportunity for employment without regard to race, sex, sexual orientation, pregnancy (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, ancestry, United States military or veteran status, color, religion, creed, marital or domestic partner status, medical condition, genetic information, national origin, citizenship status, low-income status, or mental or physical disability so long as the essential functions of the job can be performed with or without reasonable accommodation, or any other protected category under federal, state, or local law. Learn more about your rights under Federal laws and supplemental language at Labor Laws Posters (********************************* SkbztPuAwwxfs) .