Research Scientist Jobs in Corpus Christi, TX

Job Title - Research Scientist Project Duration - 12+ Months (Possible Extension) -Hybrid Role, 2 days remote/3 days in office -Candidates must be local to Austin, TX Required Skills: FE and/CFD simulation experience , COMSOL software, Experience in coding with MATLAB, Python, etc. Education: The candidate must have a PhD degree in Chemistry, Physics or equivalent field specializing in computational Chemistry. Position Summary: This position within the TEA ATG Clean Track team will involve the use of chemical engineering fundamentals and principles to develop, optimize and design new and existing wet chemical applications for the Clean Track BU. The position requires expertise in transport phenomena, thermodynamics, chemical reactions and reaction kinetics while having the ability to development predictive models and apply them to semiconductor industry applications. The candidate will provide process insight, develop detailed and innovative models via computational simulations, and spearhead process and equipment technology development leading to development, improvement, and optimization of TEL chemical/physical processes, equipment, and technologies that solves complex, high-value problems. The candidate should have a strong understanding in gas/surface chemistry, reactions, mechanisms, and computational chemistry modeling as well as experience in understanding, running, and programming scientific software in such field. Responsibilities: • Build chemical models to better understand and optimize photolithography applications consisting of single wafer chemical fluid transport and reactions • Build chemical models into simulation software to optimize tool design and/or process conditions • Model chemical reactions on semiconductor surfaces. • Prepare CFD and/or finite element simulation to understand and optimize equipment performance. • Prepare predictive models to understand process performance for next generation device length scales • Collaborate with other scientists and engineers within development team • Fully document work to provide colleagues with enough detail to maintain engineering simulations and/or code. • Strong emphasis is placed on candidates that can find solutions to difficult problems through structured project management while working in a team environment. • Good communications skills are considered critical. The candidate will communicate project goals and status updates internally and externally. • Some domestic and international travel are required. Please make sure your candidates have experience in FE and/CFD simulation experience; along for Plasma SIM & Modeling target applications experience. Education and Experience: • The candidate must have a PhD degree in Chemistry, Physics or equivalent field specializing in computational Chemistry. • Strong cause-effect analytical and troubleshooting abilities is required. • Multiscale modeling: experience using nanoscale phenomena to determine macroscale properties and predicting effects on the nanoscale when changing macroscale conditions is required. • Strong project management experience is required • Strong technical writing ability is required. • Excellent presentation and verbal communication skills are required. • Ability to execute tasks with minimal oversight is required. • Finite element and/or CFD simulation experience is required. • Extensive experience using COMSOL software is required. • Experience in coding with MATLAB, Python, etc. to solve technical problems is desired. • Knowledge of photo lithography and semiconductor industry is desirable. About Mindlance: Founded in 1999, Mindlance has been ranked as one of the fastest growing US Staffing firms by SIA for 9 consecutive years. We provide workforce solutions to Global 1000 companies in Technology, Engineering, Finance, Clinical Research, Scientific, Digital/Creative/Marketing space. Mindful of the opportunity gap, we provide balanced solutions for both employers and job seekers-elevating the standards of recruitment practice to a whole new level. Our aim is to make a difference in the lives of job seekers by providing them with opportunities that broaden career horizons and expand skill sets. We take pride in being a strong driver of mindfulness and balance at workplace. EEO: “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”

About XBiotech XBiotech is a drug Research & Development center headquartered in Austin, Texas. Our Austin facility incorporates all critical operations including discovery, research and development, drug testing, product formulation as well as clinical-regulatory affairs. XBiotech is also a fully integrated biopharmaceutical company. From pre-clinical models to clinical trial execution, from discovery to manufacturing, all activities are under one roof. XBiotech is focused on developing antibody therapeutics targeting the major medical needs of inflammatory diseases and cancer. Currently, XBiotech is growing rapidly. Our excellent facilities allow us to effectively implement and fully develop any program we adopt. We are currently planning new infrastructure and are working to change the future of medicine. Who we want: XBiotech is looking for a motivated and skilled researcher with extensive experience in immunology, virology and non-clinical assay development position in the infectious disease research area. Passion for what you do is the key to success in our environment. Multitasking and high energy is an absolute must. Open mindedness and creativity are part of your daily schedule. Qualifications · Ph.D. with 5+ years post-doctoral experience in immunology, microbiology (specifically virology) or a related field. · Experience in bioactivity assay development and neutralization assay design for therapeutics against a variety of pipeline viral and bacterial disease targets. · Experience working with virus propagation, plaque reduction neutralization assay, virus host interaction studies is required. . Experience working with aerobic and/or anaerobic pathogenic bacteria is a plus. · Experience in method development, optimization and validation of assays as a read out of an infection model is needed. · The candidate must demonstrate good oral, and written communication skills. · Must be able to manage multiple simultaneous project assignments. · Very positive interests in keeping up to date with new technologies and developments. · Ability to work well independently or in a team environment with minimal or no supervision. · Work may include weekend and off-hours. · Passion for what you do. Key Responsibilities · Direct scientific responsibilities include the design and execution of scientific research associated with XBiotech's current and future assets to support successful development of new medicines according to current industry standards and regulatory guidelines. · The candidate will be responsible for planning, executing and summarizing data generated from pre-clinical assays to support efficacy of novel anti-infective and anti-inflammatory antibodies, and to elucidate their mechanism of action. Direct laboratory efforts for bioassay, immunoassay, viral and bacterial neutralization assay development, optimization, validation and analysis support for preclinical studies as required. · Perform in vivo experiments in animal models of diseases and perform ex vivo experiments with blood and tissues from the models. · The candidate will prepare protocols, standard operating procedures, and other documentation necessary to conduct assigned experiments. · Demonstrate scientific rigor, maintain lab notebooks, and comply with good laboratory practices. Other · Prepare high quality scientific reports or presentation at R&D meetings. · Ensure that studies are completed in accordance with project timelines. · Other duties as required. Work Environment · Fast paced environment · Must be able to take on a project without constant supervision · Must be able to multitask Education · A Ph. D. degree in immunology, virology or microbiology . · Extensive knowledge in immunochemistry, viral infectious disease, viral propagation, and cell based assay development. Employee Value Proposition · Work on launching a breakthrough drug that could treat millions of people around the world · Work with the latest technology and simplest manufacturing process · Learn from an outstanding professional team equipped with experience in providing scientific services. · Work alongside staff with extensive experience in R&D, manufacturing, drug implementation and management · Pioneer in the commercialization of its antibody products using a much simpler process · From discovery to manufacturing all under one roof · Casual and friendly atmosphere · Growth potential

ERM is looking for a motivated, detail-oriented Consulting Senior Associate, Remediation to join our growing team in Austin, TX. The successful candidate will work on a variety of interesting site investigation, remediation, and hazardous waste management projects throughout Texas and our Gulf Business Unit. You may also have the opportunity to work on a variety of projects, covering the full spectrum of ERM's services. This is a great opportunity to work with ERM's technical experts to implement the latest investigation and remediation technologies, while building the required experience to obtain your professional registration. RESPONSIBILITIES: Conduct field work, including soil, sediment, groundwater, and surface water sampling, aquifer testing, drilling oversight and soil logging, soil boring and monitoring well installation, well development, purging and sampling, and construction oversight. Coordinate and direct drilling, surveying, and laboratory services. Provide construction oversight on environmental remediation projects, and operations and maintenance of environmental remediation systems. Compile and evaluate soil, groundwater, air, sediment and other environmental data. Assist in preparation of reports for submittal to regulatory agencies. Review groundwater chemistry data and prepare figures/exhibits to support regulatory reporting. Perform Phase I and II environmental site assessments to support property transfer transactions. Assist in ensuring compliance with all federal, state and local regulations. Work within quality/budget/schedule expectations and scope-specific assignments. Communicate with subcontractors, regulatory agents, tenants, and clients during field activities. REQUIREMENTS: BS in geology, hydrogeology, environmental science, or environmental engineering required. Or equivalent experience. 1+ years of experience, including willingness/interest in field assignments. Ability to work independently and as part of a team. Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports required. Ability to succeed in a consulting pace, handling multiple project assignments and maintaining flexibility while meeting strict deadlines. Detail-oriented with mechanical aptitude and hands-on troubleshooting/problem-solving skills. Environmental field work experience and 40-hour OSHA HAZWOPER certification a plus. Up to 50% regional travel Strong commitment to safety, including following established Health and Safety protocols. Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.

Kelly Science & Clinical is currently seeking candidates for a Development Scientist position at the R&D facility of a specialty chemical company in West Houston. The overall responsibilities of the position are to provide technical support for the company's products and lead application development projects to expand business opportunities. Job Responsibilities Work with R&D teams to test and evaluate new and existing polymers in the lab and pilot plant Troubleshoot and resolve technical issues by offering solutions to improve product performance Lead application development projects, ensuring they meet timelines and budgets Develop application processes and specialized test methods for new products Conduct studies on processing equipment to improve product performance Operate lab compounders, extruders, injection molders, and other equipment for testing Present experimental results and recommendations to stakeholders Collaborate with patent counsel to assess patentability and assist with patent applications Qualifications BS/MS degree in Polymer Science, Chemistry, Chemical Engineering, or related field of study Strong knowledge of polymer material science, rheology, processing, and film applications 2-5 years of experience in testing and characterization of films and plastics Familiarity with thermoplastic polymer processing, polymer rheology, and extrusion equipment Experience with developing new products Ability to travel up to 25% within the US and internationally This is a direct hire position with a Monday-Friday day shift work schedule. Salary is commensurate upon level of education and applicable experience. If you meet the above qualifications, please submit your resume for immediate consideration.

Our client is a leading biotech research company focusing on clinical research and developmental processes for new, life-changing therapeutics and treatments. Get to be a part of the groundbreaking research team, specializing in rare disease an oncology and work alongside some of the best research professionals in the field. If you are looking for career growth and professional development, this is the organization for you! Schedule: Monday-Friday 1st Pay: $55k-$60k Requirements: Bachelor's degree in science, Biology or related field with 1+ years of relevant lab experience Strong assay development and troubleshooting Perform tissue mIF and IHC staining regularly A solid understanding of current GLP and/or ISO/CAP/CLIA standards The Research Associate will focus on tissue image-mIF/IHC projects with an emphasis on performing assays and working with Scientists and relevant personnel on assay design and development, validation, and clinical sample processing in a timely manner. Responsibilities: Demonstrate independent thought and success in technical proficiency in more than one area, pay attention to detail, and collaborate with others. Independently plan and conduct drug treatment with cell lines, mIF/IHC staining on tissue or multiplex staining as needed. Support the development and implementation of protein scientific services to fulfill the Translational Research needs of Precision customers. Plan and conduct assays, perform or calibrate instrument Lecia Bondrx and Akoya Vectra Polaris, Phenocycler system, GT 450, Apostream, microscope etc. Preform assays or samples with Ficoll process, IF /IHC /ISH/Opal staining Work with Scientists and relevant personnel in the design, performance and analysis of experiments, as applicable. Perform research and development activities to support new product development. Perform assay development, validation or clinical sample processing, as needed. Operate and maintain equipment as needed. Work with managers and team members to develop project timelines and meet milestones. Assist in the training of new and existing laboratory staff in accordance with SOPs. Assist in establishing and improving all procedures and required SOP documentation. Evaluate opportunities for revision of SOPs and make necessary recommendations to improve efficiency and quality. Perform QC analyses to ensure that results meet specifications. Monitor assays and troubleshoot, as appropriate. Maintain and support safe lab practices and environment Assist with writing, reviewing and editing reports, as appropriate Other duties as assigned Escalate risks/issues in a timely manner using all established operating mechanisms available to seek guidance for mitigation. Participates in the review of new projects at late stages of contract execution. Ensure thorough review of work-scopes with accountability for assigned functional lead(s). Provide comments, as appropriate, on the feasibility, resource requirements, technical details, work-scope, and work-order clarity for projects. Provide SOP and Policy Oversight. Support functionally lead in establishing and maintaining an annual cycle to review existing SOPs for currency. Monitor to ensure that SOPs and policies are followed by all team members working within their functional area. Lead training for both existing and new team members. ** This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you**

Responsible for obtaining, researching and compiling information on claims filed for settlement. Ensures files are accurate and complete before sending to claims adjuster. Designated as point of contact to borrowers, clients and various vendors for claims that have been filed. Answer and respond to telephone inquiries from clients and borrowers Request status updates from vendors (i.e. appraisers, skip-tracers) Obtain missing information on files by contacting appropriate contact via phone, fax or email Ensure files have required information and documentation before going to the adjuster Assist borrowers, providers, and clients with problems or questions regarding their claims and/ or policies Document files with pertinent information Additional Responsibilities: Responsible for complying with state laws, policies and company procedures Other duties as assigned or required Knowledge/Skills/Abilities: Basic Microsoft Office Skills (Word, Excel, Outlook and Internet Explorer) required Typing of 45 wpm Good attention to detail Ability to multi-task Good verbal and written communication skills Good time management and organizational skills Knowledge of claims processing required Knowledge of Collateral Protection Insurance helpful Insurtrak knowledge helpful Education/Experience: High School Diploma or equivalent required Previous experience working in a claims environment required 1-3 years of general office experience required Qualifications Banking, Claims Processing, Collateral Protection Insurance, Credit Union, Remarketing

What the Senior Scientist, Bioanalytical Study Manager does at Worldwide The Senior Scientist, Bioanalytical Study leader is a role that involves overseeing the - conduct of regulated and non-regulated Bioanalytical studies. This individual collaborates with the cross-functional teams (sample management, bioanalytical labs, project management, document coordinators and quality assurance unit) for successful execution of Bioanalytical projects at Worldwide and ensures adherence to regulatory requirements. In this role they are responsible for development of project specific study plans and in ensuring projects are conducted in compliance with applicable (GLP, GCP and GCLP) regulatory guidelines. Senior Scientists provide leadership and collaborate with other functional teams in execution of projects and ensuring they oversee. They think and act strategically to align internal and externa resources to align with business needs and to meet customer's expectations. A Senior Scientist regularly participates in the production of Scientific literature such as posters, presentations, and publications. What you will do Write and implement project-specific study plans in alignment with the executed contracts and/or work orders. Assist with the review of lab manuals to ensure samples are collected in accordance with the scope of the validated method. Assist sample management in resolving sample discrepancies during shipping. Review and approve data and records associated with assigned studies including validation, post validation, stock stabilities, clinical and non-clinical studies. Ensure data, reports, and any supporting documentation is delivered to the Sponsor by the agreed upon date Lead/Assist with sponsor visits as needed What you will bring to the role Strong Scientific background. Effective time management skills Analytical problem-solving skills Ability to direct and train others in laboratory skills and project specific tasks related to their assigned studies Ability to review proposals, analytical test methods, protocols, reports, and SOPs. Your experience 8+ of relevant work experience in a Bioanalytical Laboratory Bachelor's degree (Masters preferred) in Chemistry, Biochemistry, Pharmacology, Immunology, Pharmaceutical science or High School Degree and 12 + years of experience in Bioanalytical Laboratory Minimum of 5 years' experience in a regulated (GxP) environment. Experience in Pharmaceutical, Biotechnology or Contract Research Organizations

The Product Development Scientist is responsible for developing products that meet the requirements of the customer(s) request while ensuring all safety and quality requirements are met and works with the product development team on strategic initiatives to expand Formulife's supplement product line. The Product Development Scientist will have KPIs in all stages, including but not limited to the process for specified projects spanning innovation, flavor, collaborating with customers, vendors, and internal departments, cost optimization, and commercialization. Essential Duties and Responsibilities The essential functions include, but are not limited to, the following: To develop prototype samples, plans for scale up batches for stability test, prepares product samples for stability test, stores and records samples in laboratory. Assures that materialsused, and materials manufactured meet writtenspecifications for physical and chemical attributes necessary for product manufacture Performs raw materialevaluations, documents all data collected during testing and evaluates same for completeness and correctness Performs and/or assistsin various phases of R&Dand product development activities. Process lab batches and scale up batches using scales, blenders, tablet presses, encapsulators, coaters, granulators, mills, rollers, compactors, etc. Maintain branded ingredient and raw material database Research potential ingredients based on physicalproperties such as solubility for particular form factors. Forge relationships with key suppliers, and purchasing team to keep abreast of upcoming trends, to solicit and secure opportunities for new food ideas, technologies, ingredients, and packaging materials. Lead product tastings,evaluations, etc., and analyze/record resultsin a statistical/analytical manner. Test new productsfor flavor, texture, color, nutritional content,and adherence to government and industry standards. Stay up to date on new regulations and currentevents regarding food scienceby reviewing scientific literature. Study the structure and composition of raw ingredients or the changes raw ingredients undergoin storage and processing. Develop new food items for production, based on consumerfeedback. Maintain accurate recordsof lab work, documentation of ingredients, and provide statistical evaluations and reports Perform other dutiesas assigned. Minimum Qualifications (Knowledge, Skills, and Abilities) Food safety standardsand regulations. Knowledge of cGMPs Ability to manageprocesses and procedures. Ability to manageteam members effectively. Ability to work in an environment with inside/outside extremetemperatures and in noisy environments. Knowledge of Nutritional science and formulation principles FDA, cGMP, NSF, and other regulatory compliance requirements Knowledge of Raw material and ingredient functionality Knowledge of Food safety and quality standards including HACCP and GMP Ability to conduct product development lifecycles from R&D to commercialization Knowledge of labeling regulations, supplement facts panels, and permissible health claims Scientific research and problem-solving skills Knowledge of data analysis and reporting of lab test results and production records Project management and cross-functional collaboration Ability to develop and improve supplement formulations for efficacy and stability Adapt to changing regulatory requirements and compliance measures Troubleshoot production challenges and formulation stability issues Manage multiple projects in a fast-paced environment EDUCATION: High School Diploma or equivalent required. Bachelor's degreeB.S. in Chemicalengineering, pharmaceutical sciences,Nutraceutical sciences, Nutrition, Food Engineering, Food Technology, Food Science, or similar is preferred. Employee Responsibilities Adhere to cGMP and SOPs. Report any situations that might have a negativeeffect on food safety or quality immediately to the supervisor or QA Department. Ensure food safety and quality are maintained according to company standards. Comply with policies and procedures to prepare and pack productsunder sanitary conditions that do not expose it to the risk of contamination. Operate and maintain a clean and hygienic standard of operation. Follow CompanycGMP's (Current Good Manufacturing Practices and Food Safety Policies at all times) In the absence of the Product Development Scientist, the Product Development Assistant or a same-level trained employee will overseethe daily dutiesand responsibilities regardingoperation workflow and adherence of the SOPs and cGMPs. QUALIFICATIONS: If you apply for this position,you must be eligibleto work in the U.S. without need for an employer sponsored visa (work permit). PHYSICAL DEMANDS:The work is sedentary, requiring extended period of sitting or standing to perform the work. There may be some infrequent movement from area-to-area to transport items weighing no more than 20 pounds. WORK ENVIRONMENT: While performing the primary dutiesof the job, the employeeis regularly exposedto various outdoor and indoor environments (i.e. general office, industrial complexes, food processing plants, semiconductor labs, clean rooms, etc., some of which can be hazardous). Temperature variances, high noise levels, and dusty environments may be encountered. FOOD ALLERGENNOTICE: This facility may containthe following allergens: Milk, eggs, fish, crustacean shellfish, tree nuts, peanuts, wheat & soybeans. EQUAL OPPORTUNITY EMPLOYER: We are an Equal Opportunity Employer and consider qualified applicants for employment without regard to race, ethnicity, national origin, sex, sexual orientation, gender, identity or expression, age, disability, religion, military or veteran status,or any other characteristics protected by law. YOUR RIGHT TO WORK: In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire. Job Type: Full-time Benefits: Dental insurance Disability insurance Flexible schedule Flexible spending account Health insurance Health savings account Life insurance Paid time off Parental leave Vision insurance Schedule: 8-hour shift Monday to Friday Work Location: In-person required

TH Daniels is currently partnering with a Personal Care organization who are looking for a Principal Scientist for their Skincare product portfolio. We are looking for someone who has experience within skin care, dermatology, beauty and application development in the space to come on board to help grow the organization's presence in the market. Responsibilities Work with the R&D team to define and target new product development for their key customers. Designing and developing new skincare and dermatology products. Deal with customer enquiries and target new areas of the market to expand into. Responsible for training and developing junior staff and KOL and working with the Commercial Teams to expand into new markets. Ensure close alignment with on going market trends and developments in skincare technology. Qualifications You must have experience within the personal care industry, experience with dermatology-focused products is preferred You must have a proven track record of application development and or innovation within skincare or cosmetic market A Chemical Engineering background is essential, a Masters or PhD will be preferred.

Job Title: DLE Scientist / NPI Scientist Job Status: Full-time Department: New Product Initiative (NPI) We are seeking a NPI scientist specializing in industrial water treatment solutions for our Houston office who is interested in working for a technology-driven company. This hands-on role involves working in a lab environment and potentially at commercial sites. You will contribute to the design and development of water and wastewater treatment products, particularly those related to direct lithium extraction (DLE). Essential Duties & Responsibilities: Lead the development and implementation of DLE technologies in the US. Identify and evaluate new materials, sorbents, membranes, and process configurations for DLE applications. Design and conduct laboratory and pilot-scale experiments to assess extraction performance and optimize process parameters. Analyze and interpret experimental data to drive decision-making and improvements in extraction efficiency, cost reduction, and sustainability. Support patent filings and intellectual property development related to innovative lithium extraction methods. Produce technical documentation, SOPs, and reports to support process validation and regulatory compliance. Skills/Experience/Education Required or Preferred: Ph.D., M.S., or Bachelor's Degree in Chemical Engineering, Materials Science, Chemistry, or a related field. At least 3-5 years of industry experience with DLE technologies, including ion-exchange, adsorption, solvent extraction, or membrane-based separation techniques. Examples include: Working with lithium brine resources and optimizing lithium recovery efficiency. Sorbent material development and characterization for lithium extraction. Previous involvement in pilot plant operations or commercial-scale lithium extraction projects. Excellent critical thinking, teamwork, and problem-solving abilities. Experience in process development, scale-up, and technology transfer in an industrial setting. Ability to work effectively in a fast-paced, collaborative environment with cross-disciplinary teams. Strong writing and communication skills, with the ability to present technical findings to both technical and non-technical stakeholders.

The Senior Research Associate works closely with the Director of Laboratory Operations and Chief Technology Officer to design, execute, and validate laboratory methods to support company projects. They are responsible for ensuring the accuracy and reliability of current and future laboratory procedures and compliance with regulatory requirements and industry standards. Duties, Responsibilities, and Accountabilities Coordinate the activities of junior laboratory members, providing guidance, training, and mentoring and ensuring the accuracy and reliability of laboratory results. Develop, implement, and standardize laboratory procedures and protocols. Develop and maintain effective relationships with key stakeholders. Identify and implement new technologies and methods. Ensure that laboratory equipment and supplies are properly maintained and calibrated. Develop and implement safety procedures and protocols, ensuring a safe laboratory environment. Monitor and maintain laboratory inventory. Identify and troubleshoot laboratory issues, collaborating with laboratory staff and other stakeholders to develop solutions. Conduct routine and specialized laboratory tests, following standard operating procedures and safety guidelines. Prepare and analyze laboratory samples. Record and analyze laboratory data using appropriate software and tools. Analyze laboratory data, prepare written reports, and deliver presentations with adequate analysis and interpretation. Skills Hands-on experience working with high-temperature and high-pressure equipment and analytical equipment. Experience mentoring and supervising junior laboratory members. Strong analytical and problem-solving skills. Excellent communication and interpersonal skills, with the ability to communicate complex scientific concepts to non-technical stakeholders. Ability to work effectively in a team-oriented, fast-paced, collaborative environment. Knowledge of laboratory safety procedures and protocols. Solid motivational skills with a positive mental attitude and morale. Minimum Qualifications and Experience Ph.D. in chemical engineering or a related field. 5+ years of experience in laboratory research, handling and analyzing crude oil samples using chromatography and spectroscopic methods, and handling microfluidics, core flooding, and/or other types of high-pressure & high-temperature equipment.

University Description Established in 1927, the University of Houston is a premier public research university located in the dynamic city of Houston, the energy capitol and home to most energy and chemical companies. With more than 47,000 students enrolled in over 250 academic programs, the university awards 10,000 degrees annually and boasts a strong alumni network of over 332,000 individuals. Department Description The William A. Brookshire Department of Chemical and Biomolecular Engineering is a robust program comprising 25 full-time faculty and 110 PhD students. The department has a collegial, collaborative, and diverse culture of faculty, post-doctoral and student researchers. Research Group Description The "Harold Group" led by Professor Mike Harold comprises 12 current members, doing research in chemical reaction engineering spanning the molecular to process scales. Current projects include methane abatement, methane conversion (reforming and pyrolysis), membrane reactors, and dynamic reactor & process operation. Role Description This is a full-time, on-site role for a Postdoctoral Researcher in the William A. Brookshire Department of Chemical and Biomolecular Engineering. The Postdoctoral Researcher will conduct process synthesis and analysis in the area of chemical plant repurposing. We face an exciting and challenging period in the chemical industry that requires development of more sustainable process technologies spanning feedstock, reactor and separation systems. But this must be accomplished with minimal capital. There is huge potential for retrofitting existing processes. The main goal of this project is to quantify that potential and to identify near-term opportunities. Qualifications Expertise in process synthesis and modeling (Aspen+ and related) Research and Data Analysis skills Strong problem-solving abilities Excellent written and verbal communication skills PhD in a chemical engineering Strong publication record

We have a post-doc position at UT Southwestern available! Please message me if interested in a position in translational breast tumor immunology and immunotherapy. We're doing very exciting work focused on enhancing antigen presentation. ***************************************** Postdoctoral Fellowship in Breast Cancer Immunology and Immunotherapy A postdoctoral training position is available in the laboratory of Dr. Sangeetha Reddy, (Sangeetha Reddy, M.D., Internal Medicine | Breast Cancer Immunology and Immunotherapy), in the Department of Internal Medicine, Division of Hematology and Oncology at UT Southwestern Medical Center to study Breast Cancer Immunology and Immunotherapy. Our laboratory has several exciting projects related to improving outcomes of breast cancer patients through immunotherapy. Candidates must hold a Ph.D. degree. Experience in tumor immunology leading to publication in peer-reviewed journals is recommended. Candidate should possess strong laboratory and analytical skills, a record of peer-reviewed publications, and proficiency in oral and written scientific presentations. The candidate will have the opportunity to interact and collaborate with the rich community of basic and translational scientists at UT Southwestern, as well as a team of medical oncologists. Specific duties for this position include: performing complex murine experiments testing novel immunotherapy combinations, conducting immunophenotyping assays, handling and processing patient tissue and blood specimens for immune and molecular assays in coordination with existing UT Southwestern core facilities, initiating and assisting in design of new techniques and procedures, analyzing multi-parameter research data, and assisting principal investigator in the writing of research papers for publication. Information on our postdoctoral training program and benefits can be found in our Postdoc Handbook or at *************************************** Interested individuals should send a CV, statement of interests, and a list of three references to: Sangeetha Reddy, M.D., **********************************

Our client is actively looking for a Formulation Scientist. This is an on-site position in Houston TX. You should apply if you have: 3+ years of sterile formulation experience Experience with injectables Experience with lyophilized products and strong understanding of lyo cycle development

My name is Amber Zander, a Recruiting Specialist with SCN (***************** We are partnering with a Synthetic Rubber manufacturing company who is hiring for a Sr. Technical Services Scientist. Company Highlights • Info: Corporation is a global leader in synthetic rubber manufacturing, headquartered in Taipei, Taiwan. Founded in 1973, the company specializes in producing Styrene-Butadiene Rubber (SBR), Polybutadiene Rubber (BR), Thermoplastic Elastomers (TPE), and Nitrile Butadiene Rubber (NBR) for industries such as tires, footwear, adhesives, and industrial applications. • Size: The company operates internationally, with manufacturing sites in Taiwan, China, the U.S., India, and other locations. • Employees: Approximately, 1,600 Across global operations • Dollars: reported annual revenue of approximately $993.12 million USD. • Industry: Our client operates within the chemical manufacturing sector, focusing on the production of synthetic rubber and related products. Position Highlights • Title: Sr. Technical Services Scientist • Full Time Direct Hire Background Requirements • Polymer Science & Processing Expertise - 2-5 years of experience in cast/blown/multi-layer film, SBC compounding, and polymer material science, including knowledge of rheology, extrusion, and additives. • Education in Polymer/Material Science - B.S. or M.S. in Polymer Science/Engineering, Chemistry, Chemical Engineering, or Material Science. Job Responsibilities • Technical Service & Customer Support - Provide expert technical support on Styrenic Block Copolymer (SBC) products, troubleshoot customer issues, collaborate with sales teams, and ensure alignment between customer needs and manufacturing capabilities. • Application Development & Innovation - Lead new application development projects, conduct experiments, develop specialized test methods, and optimize processing parameters for SBC applications in films, molding, and plastic modification. What is Being Offered • Challenge: The challenge of this role is balancing technical expertise and innovation with business growth, by solving complex problems, driving new applications, and collaborating across teams to meet customer needs and project goals. • Location: Katy, TX (JUST OFF TEXAS 99 FREEWAY) • Money: o Competitive Salary o Comprehensive health care benefits o Paid Vacation o 401K with Matching If you are interested and qualified, please send your updated resume as a MS Word document, and how you fit this specific position to ********************. Thank you for your consideration!

We get it: job searching takes time and attention. At Kelly , we're here to make it a whole lot easier for you. We're seeking a Research and Development Associate to work at PepsiCo, a premier company in Plano, TX. This opportunity could be the one you've been looking for. - Job Type: Full-time - Company: PepsiCo - Location: Plano, TX - Pay Rate: $20/hr - 1st Shift: 8am-5pm Mon-Fri Why you should apply to be a Research and Development Associate at PepsiCo: Get paid every week! Long-term job opportunity with a career perspective Benefits included (paid holidays, paid time off, medical, dental, vision…) Opportunity to work for a reputable and established company in the food and beverage industry Access to outstanding Kelly perks via **************************************** What's a typical day as a Research and Development Associate at PepsiCo? Ability to deliver accurate analytical results to needed timelines. Ability to work as part of a team and closely with the chemist responsible for the assigned analytical techniques. Understanding of hazardous chemicals and ability to safely handle hazardous chemicals. Ability to take on additional tasks and responsibilities based on business needs and at management discretion. Ability to prepare graphs and tables using appropriate computer software such as Microsoft Excel. This job might be an outstanding fit if you: Science or relevant degree preferred. Experience in foods or general CPG or science/engineering industry. Excel/Word/Powerpoint/MS Outlook - Microsoft product proficient Possess attention to detail Have strong communication skills Works well in a team setting, working with QA/R&D work team on other aspects of project What happens next Once you apply, you'll proceed to the next steps if your skills and experience look like a good fit. But don't worry-even if this position doesn't work out, you're still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more. Helping you discover what's next in your career is what we're all about, so let's get to work. Apply today! Please email your resume to *************************

Join us as we pursue our disruptive new vision to make machine data accessible, usable and valuable to everyone. We are a company filled with people who are passionate about our product and seek to deliver the best experience for our customers. At Splunk, we're committed to our work, customers, having fun and most importantly to each other's success. Learn more about Splunk careers and how you can become a part of our journey! The responsibilities of this role include: + Lead the development of core AI/ML models and algorithms that drive our product's key use cases in the cybersecurity and observability domains. + Collaborate closely with software engineers, applied scientists, and product managers to integrate generative AI solutions into our products and services. + Stay up to date with the latest research and developments in the field of AI/ML, and ensure that these advancements are properly incorporated into our technology roadmap. + Actively participate in cross-functional discussions and strategic decisions related to AI research directions and product roadmaps. Requirements: Knowledge, Skills, and Abilities: + PhD in Computer Science or a related field OR MS in Computer Science or related field with at least 2-3 years of industry experience + Experience training and fine tuning LLMs + Experience with time series anomaly detection + In-depth knowledge and proven track record in AI/ML technology, including deep learning, time series modeling, natural language processing, and unsupervised learning. + In-depth knowledge and proven track record in Generative AI technology and Large Language Models (LLM). + Experience developing large-scale, complex models and deploying and taking them from research to production systems. + Strong problem-solving skills and the ability to translate research insights into practical solutions that address real-world challenges. + Deep understanding of ML frameworks (e.g., TensorFlow, PyTorch) and programming languages commonly used in AI research. + Excellent communication skills with the ability to articulate complex technical concepts to both technical and non-technical audiences. + Experience in the Cybersecurity and/or Observability industry is preferred. Splunk, a Cisco company, is an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, national origin, genetic information, age, disability, veteran status, or any other legally protected basis. Note: **Base Pay Range** SF Bay Area, Seattle Metro, and New York City Metro Area Base Pay Range: $146,400.00 - 201,300.00 per year California (excludes SF Bay Area), Washington (excludes Seattle Metro), Washington DC Metro, and Massachusetts Base Pay Range: $131,760.00 - 181,170.00 per year All other cities and states excluding California, Washington, Massachusetts, New York City Metro Area and Washington DC Metro Area. Base Pay Range: $117,120.00 - 161,040.00 per year Splunk provides flexibility and choice in the working arrangement for most roles, including remote and/or in-office roles. We have a market-based pay structure which varies by location. Please note that the base pay range is a guideline and for candidates who receive an offer, the base pay will vary based on factors such as work location as set out above, as well as the knowledge, skills and experience of the candidate. **In addition to base pay, this role is eligible for incentive compensation and may be eligible for equity or long-term cash awards.** Benefits are an important part of Splunk's Total Rewards package. This role is eligible for a competitive benefits package which includes medical, dental, vision, a 401(k) plan and match, paid time off and much more! Learn more about our next-level benefits at ************************** .

Job Overview: Job Title: Scientist, Product Development Location: Frisco, Texas JOB DESCRIPTIONThe Breakthrough Innovation Product Development team's purpose is to lead the innovation and productivity agendas to grow KDP brands, transform beyond its core, and improve the profitability of our products. At KDP, our inspiration is to bring meaningful impact and that starts with our company vision -- Drink Well, Do Good! The Scientist role within Research and Development will support the product Innovation agenda to develop consumer-centric liquid beverages across existing and new platforms in several categories and brands. The Scientist will work in a dynamic environment to support the development and commercialization of new concepts and prototypes. This role positions Keurig Dr Pepper to develop and commercialize new products to delight our consumers and customers. POSITION ACCOUNTABILITIESLeads bench-top experiments, formula calculations, and develops prototypes for product tastings and sensory testing across a variety of KDP brands and product types, including alcohol containing beverages Interprets test results, writes technical reports, and effectively communicates information within the organization Verifies formula accuracy, completes formula documentation, and conducts pilot-plant trials Fully understands R&D functions and project management process to lead the commercialization of ideas to launch Partners cross functionally across R&D (Sensory, Ingredients, Nutrition, Regulatory, Flavor Technology, Chemistry, Process Engineering, and Technical Services) Influences and actively participates in Marketing and Consumer Research programs to gain consumer insights, and translate into key product concepts Manages multiples projects and represents R&D in project teams consisting of members across various departments of KDP (R&D, Marketing, Supply Chain, Sales) Delivers updates on projects within the business to key stakeholders and cross-functional peers Develop the ability to effectively communicate technical information to senior leadership Proactively identifies opportunities for improvement within function Maintains accurate and detailed record of laboratory work Work appropriately and safely in a laboratory environment Use formulation software to document lab work and formulas Demonstrate flexibility and resilience in adapting to changing business needs and priorities Ability to earn trust, maintain positive and professional relationships, and strengthen our culture of inclusionA successful candidate will exhibit a passion for innovation Requirements:B. S. in Food Science, Chemistry, Biology, or Chemical Engineering4 years of experience in a related function within food/beverage (R&D, Quality), CPG, and/or commensurate advanced education. Ability to work independently and in a team environment. Excellent written and presentation skills Works independent, excels in team-based culture and collaborates Skilled in problem solving, with a growth mindset Ability to travel is required Company Overview: Keurig Dr Pepper (NASDAQ: KDP) is a modern beverage company with a bold vision built to deliver growth and opportunity. We operate with a differentiated business model and world-class brand portfolio, powered by a talented and engaged team that is anchored in our values. We work with big, exciting beverage brands and the #1 single-serve coffee brewing system in North America at KDP, and we have fun doing it! Together, we have built a leading beverage company in North America offering hot and cold beverages together at scale. Whatever your area of expertise, at KDP you can be a part of a team that's proud of its brands, partnerships, innovation, and growth. Will you join us? We strive to be an employer of choice, providing a culture and opportunities that empower our team of ~28,000 employees to grow and develop. We offer robust benefits to support your health and wellness as well as your personal and financial well-being. We also provide employee programs designed to enhance your professional growth and development, while ensuring you feel valued, inspired and appreciated at work.

Are you looking for a new challenge? Passionate about innovation? Want to work for a global company that values integrity, teamwork, and loyalty? At LATICRETE International, we aim to be the leading construction brand trusted globally for high-performance tile and stone installation systems and building finishing solutions. We've been in business for over 65 years, family-owned for three generations, and can be found in over 100 countries. The Hartford Business Journal even named us one of Connecticut's top family-owned companies in 2017! We don't just make innovative, industry-leading products. Our purpose is to improve the built world and the lives of those who build it. We strive to connect with, engage with and improve the lives of our employees, our customers, our partners, and the global communities in which we operate. We are seeking passionate and ambitious employees who want to make a difference not just within our organization, but within their communities, our industry, and the world. If that sounds like you, then what are you waiting for? Join the family and expand your horizons! Just some of our benefits: Medical Dental Vision 401k Tuition reimbursement 12 paid holidays in addition to paid vacation and sick time Flexible spending Life Insurance, AD&D and Supplemental Insurance POSITION SUMMARY Under general supervision, the Scientist is responsible for independently formulating and conducting analytical tests in accordance with ANSI, ISO, International standards, ASTM procedures and/or other accepted methods. The Scientist is also responsible for designing complex chemical studies and experiments on organic and/or inorganic compounds for other chemists in the team. This role is also responsible for in-depth analysis of data and accurately reporting results. Scientists will demonstrate technical expertise and techniques in a specific area along with a complete understanding of projects. The scientist also demonstrates competency in planning research projects, production and Quality control. They are expected to train and work with chemists on assigned projects. Scientists are expected to use independent judgment within specific area to determine appropriate approach to project work. Additionally, they must identify new materials and develop quality control tests for new products and maintain working knowledge of all analytical equipment, procedures and techniques. ESSENTIAL DUTIES AND RESPONSIBILITIES Additional duties and responsibilities may be assigned, as necessary. Design, Develop and Validate - (50%) Under general supervision, formulate products to meet specified requirements. Devise and conduct experiments to solve increasingly complex problems. Evaluate and suggest new raw materials through increasing communication with raw material suppliers. Review and perform competitive testing and analysis as required. Maintain a clean working laboratory environment as well as properly working equipment. Ensure that all instruments that required periodic calibration and validation requirements do so per laboratory calibration/validation procedures. Comply with all laboratory, company, state and federal safety regulations. Provide Product Support - (20%) Maintain cooperative, professional attitude with all LATICRETE employees and customers. Support Technical Services requests to evaluate field complaints in specific area. Support Operations in evaluating product inconsistencies & providing disposition Participate in multi-disciplinary teams. Communicate results within R&D, cross-functional departments and Stage Gate Review meetings. Help organize and participate in field trials as required. Interact with end-use customers and contractors to understand product usage, limitations, and needs. Assist and guide the production scale-up of new products developed: Write batching formulas for the production department based upon completed and approved laboratory formulations. Follow process through to full commercialization. Determine Quality Control parameters for product testing. Design Experiments for Chemists, review data and analyze results. Data Analysis and Documentation - (10%) Responsible for documenting all work via approved methods and sharing developments via occasional technical presentations. Independently process, analyze, and interpret results and data in specific area. Summarize ongoing work and findings to colleagues during department meetings. Document work continuously according to standard practice. Summarize all project work in a formal end report. Mentor and Train New and Junior Team Members (20%) Write work instructions for R&D related test procedures. Help guide new and junior team members within the lab. Be a resource for escalations and problem solving. Impart Company knowledge of policies and procedures to help them orient to the organization. Consistently uphold Company culture through positive communications, managing conflict and fostering an open and constructive environment. REQUIRED SKILLS & QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and Experience: BS in Chemistry, Material Science, Polymer Science or relevant Engineering discipline is required. MS a plus. 8+ years of construction materials formulation experience with a proven track record of successful New Product Development, Scientific report writing, and skills in mentoring people. Specialized Skills and Experience: Experience formulating products in a research and development lab environment in a specific area of the construction industry. Experience with Production/Operations, Product Management, QC, ISO processes, Analytical Chemistry, Product Development, Finance, Accounting and Marketing departments. Must be familiar with the process of researching patents, writing invention disclosures, and other publications within the industry. Demonstrated analytical ability in specific area, well organized, detail oriented, and systematic in documenting results. Demonstrated verbal and written communication skills in order to present and write reports. Ability to organize and present results in a clear concise manner. Must be able to analyze data independently and apply some specialized knowledge (e.g. DOE and statistical methods to solve problems). Must be a self-starter and able to multi-task. Computer skills: Intermediate to Advanced knowledge of Microsoft Office 365 (Word, Excel, PowerPoint), Outlook and other specialty software systems as required. Physical Requirements: Lift: Must be able to lift and/or carry a minimum of 50 pounds. Push/Pull: Must be able to push/pull 50 pounds. Standing: Must be able to stand at least 50% of the day. Sitting: Must be able to sit at least 50% of the day. Travel: Domestic travel may be required as needed #LI-DS1