validation scientist

Labcorp

<div>At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.
We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. We put our trust in science and in one another. This is your chance to become part of a team that helps to bring the miracles of medicine to market sooner, as Labcorp Drug Development has helped pharmaceutical and biotech companies develop one-third of all prescription medicines on the market today.
We are seeking a LC/MS Validation Scientist III to join our Bioanalytical team in Indianapolis, IN. As a Validation Scientist III, you will perform method validation, method update and stability testing using a variety of analytical techniques in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. In addition, you will provide downstream support of methods to associated groups and serve as a bioanalytical resource to the broader business.
Duties and Responsibilities:<ul><li>
Organize and perform routine to advanced level of method validation/testing (and all associated activities) with independence and efficiency in compliance with appropriate SOPs and regulatory agency guidelines.</li><li>
Display advanced data interpretation and analytical instrumentation skills and respond to difficult procedural, technical, and quality questions with minimal guidance.</li><li>
Assist in writing and review of reports, methods, protocols, and SOPs and maintain complete study documentation in compliance with regulatory guidelines (e.g. GLP and GCP) and department processes.</li><li>
Inform Lead Scientist and/or management of any problems and/or deviations that may affect the integrity of the data and recommend corrective action.</li><li>
Write and review training materials and deliver training/mentorship of staff in relevant techniques, procedures and provide expert advice on training requirements.</li><li>
Support communications with external clients and other team members.</li><li>
Participate in new equipment, instrument and methodology assessment and qualifications.</li><li>
Demonstrate advanced time management skills and manages work on multiple assigned projects in a given week, and liaise and coordinate work activities with team members in order to deliver data.</li><li>
Support others in their duties to ensure all scheduled operational activities are completed on each given day by effective and concise communication with team members, and ability to listen and discuss ideas in an open and professional manner.</li><li>
Participate in process improvement initiatives.</li></ul>
Education/Experience:<ul><li>
Bachelor&rsquo;s Degree in Life Sciences, Pharmaceutical science or Chemistry with 3 years of relevant work experience or Master&rsquo;s Degree with at least 1 year of relevant work experience in LC/MS method validation</li><li>
Excellent communication and interpersonal skills</li><li>
Proven ability to prioritize and manage time.</li><li>
Excellent attention to detail</li><li>
Able to utilize word processing, database, spreadsheet, and specialized software.</li><li>
Work experience in GLP/GCP environment is a plus</li></ul>
Application Window: 12/30/2025 thru 1/5/2026
Pay Range: $69k - $81k annually
All job offers will be based on a candidate&rsquo;s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.
Benefits:
Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN &amp; Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.
Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.</div>

LCMS Validation Scientist III

Genalyte, Inc.

<div>ABOUT GENALYTE
At Genalyte, we're revolutionizing diagnostic testing to empower a healthier future. We believe that timely and accurate health insights shouldn't be a luxury, but a necessity. We are driven by a vision where advanced diagnostic capabilities are accessible, efficient, and seamlessly integrated into healthcare. Genalyte is more than just a laboratory; we are advocates for health empowerment, dedicated to providing insights that can transform lives and communities. 
WHY WORK FOR US
We believe in investing in our employees' well-being and success. As a valued member of our team, you'll have access to a comprehensive benefits package, including competitive salary, health, dental, and vision insurance, and generous paid time off. Additionally, we offer stock ownership and equity participation, providing you with the opportunity to directly share in the success and growth of the company. Join us in shaping the future of healthcare while building a rewarding career. 
POSITION SUMMARY 
We are seeking a Scientist II to lead our Development &amp; Validation operations and provide expertise across our organization on performing, developing and validating hematology, serology, and chemistry assays. In this role, you will lead with groups in R&amp;D, Quality, Regulatory and Manufacturing. In addition to overseeing daily operational activities, you will play a significant role in product development including leading GLP studies for FDA submissions and contributing to resolving design transfer and quality control challenges. You will also participate in research collaborations internally and with external partners. This posting is intended to fill two open positions. 
ESSENTIAL FUNCTIONS &amp; RESPONSIBILITIES
These may include but are not limited to:<ul><li>
Draft and finalize protocols and reports for analytical studies</li><li>
Lead the existing team with strong competencies in serology, chemistry and other immunoassay practices and execution of controlled performance studies</li><li>
Design, develop and optimize quantitative immunoassays for submission to the FDA for 510(k) clearance assessing feasibility through initial phases and through the design control process</li><li>
Analyze data for assay and process improvement and report findings to team and senior leadership</li><li>
Investigate and troubleshoot problem areas to recommend product improvements</li><li>
Meet milestones for product development timelines</li><li>
Work as part of a multi-disciplinary team with other chemists, data scientists, engineers and manufacturing personnel</li><li>
Maintain compliance with all company policies, quality systems, design control and procedures</li><li>
Document results, protocols, SOPs, etc</li><li>
Manage external studies in collaboration with key opinion leaders (KOLs) and support scientific publications</li><li>
Oversee collaborations with clinical trial partners, study sites, and contribute to any and all internal documents</li><li>
Actively communicates project status, challenges, concerns, and resource constraints to area management</li><li>
Writes design control documentation and executes/oversees associated test and risk management activities</li><li>
Works with R&amp;D to develop, optimize and integrate assay V&amp;V</li><li>
Ensures an appropriate and effective level of understanding of project needs to appropriately schedule and complete activities as committed</li><li>
Supports improvement verifications, validations, and transfers</li><li>
Develops, reviews, or approves execution protocols and group generated data</li><li>
Oversee studies, reviews protocol execution, and approves summary reports</li></ul> 
EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS AND ABILITIES:<ul><li>
A minimum of a Master&rsquo;s degree in chemistry, biochemistry or similar with 5+ years of experience in Assay Development</li><li>
Experience with team direction and mentorship</li><li>
Experience with FDA and 510(k) submission process</li><li>
Experience in some or all of the following areas:<ul><li>
Antibody and protein biochemistry, surface energy modification, assay development</li>
Experimental design (DOEs, etc), statistical analysis, power analysis, and detailed understanding of precision, uncertainty, error propagation, etc.<li> 510(k) submissions and study requirements, verification and validation of assay designs</li><li>
Chemical kinetics, silicon photonics, microfluidics</li><li>
Experience with large data sets &amp; analysis &amp; software (jmp, minitab or similar)</li><li>
Working with quality assurance and quality control teams</li></ul></li><li>
Standard assay laboratory equipment (pipets, microscales, vortexers, centrifuges, etc.)</li><li>
Analytical chemistry equipment (fluorimeters, spectrophotometers, chromatography, etc.)</li><li>
Experience with protein or small molecule conjugation techniques, particle chemistry, particle size analysis and flow cytometry.</li><li>
Experience with development of in vitro diagnostic for biomarkers in the Point of Care setting</li><li>
Demonstrated skills in carrying out innovative research with minimal guidance in an accurate, effective manner</li><li>
Proven ability to functionally direct junior research staff</li><li>
Experience identifying and implementing new technologies or improvements of existing technologies for any of the following: marker discovery, marker validation, product development, DFM and product manufacturing</li><li>
Knowledge of scientific principals and concepts</li><li>
Excellent organizational skills and ability to manage multiple tasks/projects simultaneously</li><li>
Ability to plan and execute experiments to prove feasibility, develop new processes and set specifications, characterize materials and set specifications, and troubleshoot problems</li><li>
Demonstrated ability to consistently meet proposed objective timelines, apply competent use of project planning and project management skills</li><li>
Knowledge of quality system regulations and processes</li><li>
Understand theoretical basis for analytical instrumentation</li><li>
Detail-oriented and able to work with a variety of people on multiple tasks, with effective prioritization of duties</li><li>
Experience identifying and implementing new technologies for marker discovery, marker validation, product development, and product manufacture is also important</li><li>
Knowledgeable of federal and other regulations, e.g. QSR&rsquo;s, ISO, ISO 13485, CMDR</li><li>
Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities</li><li>
General presentation &amp; spreadsheet analysis software</li><li>
Mathematical curve fitting packages</li><li>
Statistical analysis software and routines</li></ul> 
The base range for this role is $100,000 - $145,000 per year. Individual pay may vary based on additional factors, including but not limited to, job-related skills, experience, work location, and relevant education or training. In addition to base salary, Genalyte provides generous benefits, equity opportunities, and for some roles, participation in our annual target bonus plan. 

ZsopeY8HVe</div>

Scientist I/ Scientist II, Validation

<div>
 &nbsp;
 
 
 
 
 
 
 
 
 ABOUT GENALYTE&nbsp;
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 At Genalyte, we're revolutionizing diagnostic testing to empower a healthier future. We believe that timely and accurate health insights shouldn't be a luxury, but a necessity. We are driven by a vision where advanced diagnostic capabilities are accessible, efficient, and seamlessly integrated into healthcare. Genalyte is more than just a laboratory; we are advocates for health empowerment, dedicated to providing insights that can transform lives and communities.
 
 
 
 
 
 
 
 
 &nbsp;
 
 
 
 
 
 
 
 
 WHY WORK FOR US&nbsp;
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 We believe in investing in our employees' well-being and success. As a valued member of our team, you'll have access to a comprehensive benefits package, including competitive salary, health, dental, and vision insurance, and generous paid time off. Additionally, we offer stock ownership and equity participation, providing you with the opportunity to directly share in the success and growth of the company. Join us in shaping the future of healthcare while building a rewarding career.
 
 
 
 
 
 
 
 
 &nbsp;
 
 
 
 
 
 
 
 POSITION SUMMARY
 
 
 
 
 
 
 
 
 
 
 
 
 
 We are seeking a&nbsp; Scientist II to lead our Development &amp; Validation operations and provide expertise across our organization on performing, developing and validating&nbsp; hematology, serology, and chemistry assays.&nbsp; In this role, you will lead with groups in R&amp;D, Quality, Regulatory and Manufacturing.&nbsp; In addition to overseeing daily operational activities, you will play a significant role in product development including leading GLP studies for FDA submissions and contributing&nbsp; to resolving design transfer and quality control challenges.&nbsp; You will also participate in research collaborations internally and with external partners.
 
 
 
 
 
 
 
 
 
 
 
 
 This posting is intended to fill two open positions.&nbsp;
 
 
 
 
 
 
 
 &nbsp;
 
 
 
 
 
 
 
 ESSENTIAL FUNCTIONS &amp; RESPONSIBILITIES
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 These may include but are not limited to:&nbsp;
 
 
 
 
 
 
 
 <ul>
 <li>
 
 
 
 
 
 
 Draft and finalize protocols and reports for analytical studies
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Lead the existing team with strong competencies in serology, chemistry and other immunoassay practices and execution of controlled performance studies
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Design, develop and optimize quantitative immunoassays for submission to the FDA for 510(k) clearance assessing feasibility through initial phases and through the design control process&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Analyze data for assay and process improvement and report findings to team and senior leadership&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Investigate and troubleshoot problem areas to recommend product improvements&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Meet milestones for product development timelines&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Work as part of a multi-disciplinary team with other chemists, data scientists, engineers and manufacturing personnel
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Maintain compliance with all company policies, quality systems, design control and procedures&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Document results, protocols, SOPs, etc
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Manage external studies in collaboration with key opinion leaders (KOLs) and support scientific publications
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Oversee collaborations with clinical trial partners, study sites, and contribute to any and all internal documents&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Actively communicates project status, challenges, concerns, and resource constraints to area management&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Writes design control documentation and executes/oversees associated test and risk management activities&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Works with R&amp;D to develop, optimize and integrate assay V&amp;V&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 
 Ensures an appropriate and effective level of understanding of project needs to appropriately schedule and complete activities as committed&nbsp;
 
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 
 Supports improvement verifications, validations, and transfers&nbsp;
 
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 
 Develops, reviews, or approves execution protocols and group generated data&nbsp;
 
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 
 Oversee studies, reviews protocol execution, and approves summary reports&nbsp;
 
 
 
 
 
 
 
 </li>
 </ul>
 &nbsp;
 
 
 
 
 
 
 
 EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS AND ABILITIES:
 
 
 
 
 
 
 
 <ul>
 <li>
 </li>
 <li>
 
 
 
 
 
 
 A minimum of a Master&rsquo;s degree in chemistry, biochemistry or similar with 5+ years of experience in Assay Development&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Experience with team direction and mentorship&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Experience with FDA and 510(k) submission process&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Experience in some or all of the following areas:&nbsp;
 
 
 
 
 
 
 <ul>
 <li>
 
 
 
 
 
 
 Antibody and protein biochemistry, surface energy modification, assay development
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Experimental design (DOEs, etc), statistical analysis, power analysis, and detailed understanding of precision, uncertainty, error propagation, etc. &cir; 510(k) submissions and study requirements, verification and validation of assay designs&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Chemical kinetics, silicon photonics, microfluidics&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Experience with large data sets &amp; analysis &amp; software (jmp, minitab or similar)&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Working with quality assurance and quality control teams&nbsp;
 
 
 
 
 
 
 </li>
 </ul>
 </li>
 <li>
 
 
 
 
 
 
 Standard assay laboratory equipment (pipets, microscales, vortexers, centrifuges, etc.)&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Analytical chemistry equipment (fluorimeters, spectrophotometers, chromatography, etc.)&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Experience with protein or small molecule conjugation techniques, particle chemistry, particle size analysis and flow cytometry.&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Experience with development of in vitro diagnostic for biomarkers in the Point of Care setting
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Demonstrated skills in carrying out innovative research with minimal guidance in an accurate, effective manner&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Proven ability to functionally direct junior research staff &nbsp;&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Experience identifying and implementing new technologies or improvements of existing technologies for any of the following: marker discovery, marker validation, product development, DFM and product manufacturing&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Knowledge of scientific principals and concepts &nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Excellent organizational skills and ability to manage multiple tasks/projects simultaneously &nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Ability to plan and execute experiments to prove feasibility, develop new processes and set specifications, characterize materials and set specifications, and troubleshoot problems   &nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Demonstrated ability to consistently meet proposed objective timelines, apply competent use of project planning and project management skills    &nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Knowledge of quality system regulations and processes   &nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Understand theoretical basis for analytical instrumentation&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Detail-oriented and able to work with a variety of people on multiple tasks, with effective prioritization of duties
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Experience identifying and implementing new technologies for marker discovery, marker validation, product development, and product manufacture is also important&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Knowledgeable of federal and other regulations, e.g. QSR&rsquo;s, ISO, ISO 13485, CMDR&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 General presentation &amp; spreadsheet analysis software&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Mathematical curve fitting packages&nbsp;
 
 
 
 
 
 
 </li>
 <li>
 
 
 
 
 
 
 Statistical analysis software and routines&nbsp;
 
 
 
 
 
 
 </li>
 </ul>
 &nbsp;
 
 
 
 
 
 
 
 
 The base range for this role is $100,000 - $145,000 per year. Individual pay may vary based on additional factors, including but not limited to, job-related skills, experience, work location, and relevant education or training. In addition to base salary, Genalyte provides generous benefits, equity opportunities, and for some roles, participation in our annual target bonus plan.
 
 
 
 
 
 
 
 
 
 
 &nbsp;
</div>

<div></div><div><div><div><div><ul><div>2 - 3 Years</div>
<div></div><div>1 Opening</div>
 <div>Hyderabad</div></ul></div><div> 
<div><div>
</div></div></div></div><div></div><div><h3 class="jobSectionHeader">Role description</h3> 
<div><div> 
Who we are:</div>
<div>
At UST, we help the world&rsquo;s best organizations grow and succeed through transformation. Bringing together the right talent, tools, and ideas, we work with our client to co-create lasting change. Together, with over 30,000 employees in 25 countries, we build for boundless impact&mdash;touching billions of lives in the process. Visit us at .</div> 
<div></div>
<div>
The Opportunity:</div>
<div>
 Validation Engineer</div>
<div></div>
<div>Key Responsibilities
</div><ul><li> Develop and execute validation plans for USB, audio, display, storage, and power management features. Run standard test suites such as Windows HCK/HLK and internal frameworks (e.g., NVIDIA tools).</li></ul>
<ul><li> Triage issues using tools like Event Viewer, Device Manager, Dmesg, serial/UART logs.</li></ul>
<ul><li> Perform firmware regression testing to ensure backward compatibility and bug verification.</li></ul>
<ul><li> Simulate complex use cases such as device removal during sleep/resume, multi-monitor setups, and hot-plug stress scenarios.</li></ul>
<ul><li> Reproduce failures and isolate issues to the hardware, firmware, or driver layer using structured debug. Log and track bugs using tools such as Jira, Bugzilla, or internal portals. Work closely with BIOS, driver, and hardware engineering teams to analyze and resolve open issues.
</li></ul><ul><li> Contribute to validation coverage reporting, defect dashboards, and triage documentation. Support reproduction and debugging of field/customer-reported issues.</li></ul>
<div>
Required Skills:
</div><ul><li> Strong knowledge of Windows-based system validation. Experience with firmware, driver, or OS-level debugging. Familiarity with validation tools and test automation environments.
</li></ul><ul><li> Good understanding of platform subsystems: USB, audio, display, storage, power.</li></ul>
<ul><li> Proficiency in defect tracking systems and triage workflows. Excellent communication and cross-team collaboration</li></ul> 
<div></div>
<div>
 Desired Skills:
</div><ul><li> Bachelor&rsquo;s degree in Computer Engineering, Electrical Engineering, or related field.</li></ul>
<ul><li> 5+ years of experience in platform/system validation, firmware testing, or triage engineering.</li></ul>

Skills
<ul><li> Windows Os,Debugging,Debugging Tools</li></ul> 
<div></div>
<div>
What we believe:</div>
<div>
We&rsquo;re proud to embrace the same values that have shaped UST since the beginning. Since day one, we&rsquo;ve been building enduring relationships and a culture of integrity. And today, it's those same values that are inspiring us to encourage innovation from everyone, to champion diversity and inclusion and to place people at the centre of everything we do.</div>
<div>
Humility:</div>
<div>
We will listen, learn, be empathetic and help selflessly in our interactions with everyone.</div>
<div>
Humanity:</div>
<div>
Through business, we will better the lives of those less fortunate than ourselves.</div>
<div>
Integrity:</div>
<div>
We honour our commitments and act with responsibility in all our relationships.</div> 
<div></div>
<div>
Equal Employment Opportunity Statement</div> 
<div></div>
<div>
UST is an Equal Opportunity Employer. We believe that no one should be discriminated against because of their differences, such as age, disability, ethnicity, gender, gender identity and expression, religion, or sexual orientation.</div> 
<div></div>
<div>
All employment decisions shall be made without regard to age, race, creed, colour, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law.</div><div> 

UST reserves the right to periodically redefine your roles and responsibilities based on the requirements of the organization and/or your performance.</div> 
<div></div>
<ul><li>To support and promote the values of UST.</li></ul>
<ul><li>Comply with all Company policies and procedures</li></ul></div>
<h3 class="jobSectionHeader">Skills</h3>
<div>Windows Os,Debugging,Debugging Tools</div></div></div></div>
 <div><h3 class="jobSectionHeader">About UST</h3>
<div>UST is a global digital transformation solutions provider. For more than 20 years, UST has worked side by side with the world&rsquo;s best companies to make a real impact through transformation. Powered by technology, inspired by people and led by purpose, UST partners with their clients from design to operation. With deep domain expertise and a future-proof philosophy, UST embeds innovation and agility into their clients&rsquo; organizations. With over 30,000 employees in 30 countries, UST builds for boundless impact&mdash;touching billions of lives in the process.</div></div>

Validation Engineer

Brillio LLC

<div><h1 class="jobSectionHeader">Senior Data Scientist - R01558827</h1>
<div>Senior Data Scientist</div><h6 class="jobSectionHeader">
Primary Skills</h6><ul><li>
Problem Formulation (Business problem to Data Science Problem), OKR Validation against statistical measures, Data Wrangling, Data Storytelling &amp; Insight Generation, Problem Solving, Excel VBA, Data Curiosity, Technical Decision Making (How many iterations to go for vs when to stop iterating), Communication &amp; Articulation: Vocal &amp; Written, Business Acumen (Consume new domains quickly to learn through data), Design Thinking, Data Literacy
</li></ul><h6 class="jobSectionHeader">Specialization</h6><ul><li>
Data Science Foundation: Data Scientist
</li></ul><h6 class="jobSectionHeader">Job requirements</h6><ul><li>
Need B1 resource for Senior Data Scientist with Experience: 6+ Below is JD: Design and develop intelligent, autonomous AI agents using frameworks like LangChain, AutoGPT, CrewAI, etc. Work with LLMs (GPT-4, Claude, LLaMA, Mistral) to create scalable, enterprise-grade agentic solutions. Build and optimize ML/DL models to power decision-making for agents. Collaborate with cross-functional teams to deliver AI-first digital experiences. Stay on the edge of innovation in Generative AI, RAG, Vector Databases (FAISS/Pinecone), Prompt Engineering, and more. Experience in Data Science / Machine Learning / AI. 4 plus years of Hands-on with Python, LLM APIs, and ML/DL libraries (PyTorch, TensorFlow, Scikit-learn). Real-world experience with Agentic AI frameworks and orchestration tools. Strong understanding of cloud-based AI deployments (Azure/AWS/GCP). A growth mindset with curiosity for emerging AI technologies. Working experience with GitHub</li></ul></div>

Senior Data Scientist – R01558827

<div><h1 class="jobSectionHeader">Senior Data Scientist - R01558826</h1>
<div>Senior Data Scientist</div><h6 class="jobSectionHeader">
Primary Skills</h6><ul><li>
Problem Formulation (Business problem to Data Science Problem), OKR Validation against statistical measures, Data Wrangling, Data Storytelling &amp; Insight Generation, Problem Solving, Excel VBA, Data Curiosity, Technical Decision Making (How many iterations to go for vs when to stop iterating), Communication &amp; Articulation: Vocal &amp; Written, Business Acumen (Consume new domains quickly to learn through data), Design Thinking, Data Literacy
</li></ul><h6 class="jobSectionHeader">Specialization</h6><ul><li>
Data Science Foundation: Data Scientist
</li></ul><h6 class="jobSectionHeader">Job requirements</h6><ul><li>
Need B1 resource for Senior Data Scientist with Experience: 6+ Below is JD: Design and develop intelligent, autonomous AI agents using frameworks like LangChain, AutoGPT, CrewAI, etc. Work with LLMs (GPT-4, Claude, LLaMA, Mistral) to create scalable, enterprise-grade agentic solutions. Build and optimize ML/DL models to power decision-making for agents. Collaborate with cross-functional teams to deliver AI-first digital experiences. Stay on the edge of innovation in Generative AI, RAG, Vector Databases (FAISS/Pinecone), Prompt Engineering, and more. Experience in Data Science / Machine Learning / AI. 4 plus years of Hands-on with Python, LLM APIs, and ML/DL libraries (PyTorch, TensorFlow, Scikit-learn). Real-world experience with Agentic AI frameworks and orchestration tools. Strong understanding of cloud-based AI deployments (Azure/AWS/GCP). A growth mindset with curiosity for emerging AI technologies. Working experience with GitHub</li></ul></div>

Senior Data Scientist – R01558826

United Pharma Technologies Inc

<div>
 
 
 Job Title: QC Scientist
 
 
 
 
 Location: North Carolina (Onsite)
 
 
 
 
 
 
 
 Job Description:
 
 
 
 Seeking a
 
 QC Scientist
 
 with 2&ndash;5 years of experience in a regulated medical or pharmaceutical environment. The role involves routine quality control testing, GMP documentation, and support of laboratory investigations to ensure product quality and compliance.
 
 
 
 
 
 
 Responsibilities:
 
 
 <ul>
 <li>
 Perform QC testing using techniques such as HPLC, GC, UV, FTIR, and wet chemistry
 </li>
 <li>
 Document and review results per GMP/FDA requirements
 </li>
 <li>
 Support OOS/OOT, deviations, CAPA, and method validation activities
 </li>
 <li>
 Maintain SOPs, lab records, and instrument documentation
 </li>
 </ul>
 
 
 
 
 
 Requirements:
 
 
 <ul>
 <li>
 BS/MS in Chemistry, Biology, or related field
 </li>
 <li>
 2&ndash;5 years QC lab experience in medical/pharma industry
 </li>
 <li>
 Strong knowledge of GMP and regulatory guidelines
 </li>
 </ul>
 
 
</div>

Quality Control Scientist

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Quality Control Scientist