research scientist

Reliance Industries Limited

<div>
 <strong>
  Job Responsibilities :
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Ensure completion of experiments and generate accurate and reproducible data from experiments. Develop relevant models and validation of the same.
  </li>
  <li>
   Supervise and execute laboratory / pilot plant experiments pertaining to the relevant research area such as sample preparation using various methods, sample characterization using various analysis &amp; evaluation of the concerned samples.
  </li>
  <li>
   Organize facilities for experiments in research such as chemicals, equipment, analytical methods etc.
  </li>
  <li>
   Participate in pilot plant operations / studies, utilize results as boundary conditions for model development
  </li>
  <li>
   Support to plant operations
  </li>
  <li>
   Collect data and conduct relevant analysis
  </li>
  <li>
   Uploading reports on portal
  </li>
  <li>
   Preparation of Internal Technical Report
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Job Profile:
 </strong>
 Research Scientist (J Level) - Specialty Inorganic Chemicals, Vadodara
 <br/>
 <br/>
 The Research Scientist will be responsible for driving research programs in specialty inorganic chemicals, focusing on improving inorganic chemical synthesis and inorganic additives for polymers and glass applications. The role includes laboratory experimentation, data analysis, technical reporting, process scale-up support, and collaboration with cross-functional teams to translate research outcomes into practical applications.
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Plan, design, and execute research programs in specialty inorganic chemicals.
  </li>
  <li>
   Conduct laboratory synthesis, process optimization, and scale-up studies.
  </li>
  <li>
   Identify innovative approaches for developing new inorganic materials and solutions.
  </li>
  <li>
   Provide technical support to plant operations and assist in plant troubleshooting.
  </li>
  <li>
   Prepare high-quality Internal Technical Reports, patents, and research publications.
  </li>
  <li>
   Ensure record-keeping in compliance with Standard Laboratory Practices (SLP).
  </li>
  <li>
   Review and finalize draft reports and project documentation.
  </li>
  <li>
   Supervise data maintenance and ensure reproducibility and traceability of experiments.
  </li>
  <li>
   Identify opportunities for outsourcing expertise, collaborations, or consultancy in specialized areas.
  </li>
  <li>
   Mentor and guide subordinates, ensuring effective knowledge sharing across the team.
  </li>
  <li>
   Ensure adherence to HSE procedures and practices in laboratory and pilot plant operations.
  </li>
  <li>
   Conduct Process Hazard Analysis (PHA) and PSSR for inorganic chemical research.
  </li>
  <li>
   Prioritize research projects, set milestones, and track progress in alignment with organizational goals.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Skills &amp; Competencies
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Strong expertise in inorganic chemical synthesis and new material development.
  </li>
  <li>
   Sound knowledge of laboratory safety practices, and HSE compliance.
  </li>
  <li>
   Excellent planning, project management, and experimental design skills.
  </li>
  <li>
   Strong analytical thinking, problem-solving, and decision-making abilities.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Education Required
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Ph.D. in Chemistry with a strong research background in inorganic chemistry and new inorganic material synthesis.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Experience Desired
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   1&ndash;3 years of post-Ph.D. experience in specialty inorganic chemical synthesis, new material development, and characterization.
  </li>
  <li>
   Hands-on experience with inorganic synthesis techniques, catalyst support materials, adsorbents, and inorganic additives.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Education Requirement :
  <br/>
  <br/>
 </strong>
 PhD in Biology/Chemistry/Chemical Engineering with specialization in relevant research area
 <br/>
 <br/>
 <strong>
  Experience Requirement :
  <br/>
  <br/>
 </strong>
 <strong>
  Minimum 2-3 Years Of Research Experience
  <br/>
  <br/>
 </strong>
 <strong>
  Skills &amp; Competencies :
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Conduct literature survey in the area of research and compile information for dissemination &amp; critical analysis.
  </li>
  <li>
   Develop work method and prepare SOPs for experiments in research including designing &amp; planning of experiments.
  </li>
  <li>
   Prepare/Use simulation models.
  </li>
  <li>
   Study technology offers/ process engineering documents
  </li>
  <li>
   Perform process engineering design activities such as using relevant tools
  </li>
  <li>
   Familiar with applicable guidelines /codes / standards / legislations relevant to field of research
  </li>
 </ul>
</div>


Research Scientist ( 82209156 )

CloudFirst

<p>Overview</p><p>The Research Scientist role at GRAG AI Factory is a challenging, dynamic, and highly innovative opportunity for those eager to shape the future of artificial intelligence. As a member of our world-class team, you will drive transformative research by generating breakthrough ideas, developing enterprise-ready solutions, and advancing the field of AI through both collaborative projects and individual technical leadership.</p><p>Key Responsibilities</p><p>&middot; Innovation &amp; Idea Generation: Conceive and refine novel concepts in artificial intelligence, machine learning, generative AI, and related fields.</p><p>&middot; Solution Development: Collaborate with interdisciplinary teams to transform research ideas into practical solutions, algorithms, and applications.</p><p>&middot; Rapid Prototyping: Build and test functional prototypes that demonstrate the technical viability and business value of your research.</p><p>&middot; Research Publication: Author high-quality research papers for leading international conferences and journals, advancing the scientific community and GRAG&rsquo;s reputation.</p><p>&middot; Enterprise Value Demonstration: Work with product and engineering teams to showcase how your research can create real impact in enterprise settings.</p><p>&middot; Knowledge Sharing: Present findings to both internal and external stakeholders; contribute to workshops, demos, and thought leadership.</p><p>&middot; Mentorship: Support and guide junior researchers, interns, and team members to foster a creative and rigorous research culture.</p><p>Qualifications</p><p>&middot; PhD or Master&rsquo;s in Computer Science, Engineering, Mathematics, or a related field (exceptional candidates with strong research track records may be considered).</p><p>&middot; Proven experience in AI/ML research with publications in respected conferences or journals.</p><p>&middot; Proficiency in programming languages such as Python, C++, or Java, and experience with modern AI/ML frameworks.</p><p>&middot; Demonstrated ability to build prototypes and translate research into robust solutions.</p><p>&middot; Strong problem-solving, analytical, and communication skills.</p><p>&middot; Ability to work effectively in fast-paced, cross-functional teams.</p><p>&middot; Enthusiasm for learning new technologies and exploring uncharted territory.</p><p>Nice to Have</p><p>&middot; Experience applying research in enterprise, robotics, generative AI, or neural/emotional intelligence domains.</p><p>&middot; Record of patents, open-source contributions, or industry impact.</p><p>&middot; Familiarity with cloud computing, big data, and scalable system design.</p><p>Why Join GRAG AI Factory?</p><p>&middot; Be at the forefront of AI innovation and deep tech research.</p><p>&middot; Collaborate with top-tier researchers and engineers on impactful global projects.</p><p>&middot; Enjoy a culture that rewards creativity, curiosity, and real-world results.</p><p>Ready to invent the next big breakthrough? Join GRAG AI Factory and help shape the future.</p><p>Job Type: Full-time</p><p>Pay: AED2,000.00 - AED3,000.00 per month</p>

Research Scientist

Nationwide Children's Hospital

<div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div>Overview:</div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><div></div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><br>
Job Description Summary:</div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><div></div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><br>
Job Description:</div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><div></div><div><br>
Research Scientist, Research Institute at Nationwide Children&rsquo;s Hospital, Columbus, OH. Design experiments and protocols for conducting research to develop vaccines for two important respiratory viruses: RSV and SARS-CoV-2. Lead the project to develop a novel live attenuated respiratory syncytial virus (RSV) vaccine that will be delivered intranasally to protect children between 1 and 5 years and adults over 60 from severe RSV disease. Make cDNA clones containing the genes for critical immunogenic viral proteins and use them to produce native viral proteins or modified versions that are optimal targets for the protective immune response. Produce and test attenuating mutations in RSV that weaken its ability to replicate and cause disease but enhance its immunogenicity. Evaluate the immune response induced by these vaccines and quantifying its ability to prevent infection of primary human airway cell cultures and small animal models. From the results of studies, help to develop hypotheses for further improvements in these vaccines, prepare technical abstracts, scientific articles for review and publication in top virology journals, and presentations to colleagues in other labs and at virological meetings. Min. req incl: Ph.D. in Microbiology, Virology, Biomedical Sciences, plus 5 years of experience in molecular biology, cell biology, and virology; 5 years of research experience identifying important research questions, developing productive approaches, designing and performing experiments, and interpreting the results; 5 years of experience researching RSV and SARS-Cov-2; 3 years of experience assembling cDNA clones and using them to rescue live attenuated RSV vaccine candidate viruses; and 3 years of experience producing and purifying viral proteins for use in experimental immunizations and in the detection of antibodies specific for the RSV glycoproteins. Apply to job requisition &ndash; R-18835 at <div>Careers</div></div><div></div><div><br>
&quot;The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individuals so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under their supervision. EOE M/F/Disability/Vet&quot;</div></div>

PI Health Sciences Ltd

<div>
 <p>
  <strong>
   Job Title: Research Scientist &ndash; Process R&amp;D
  </strong>
 </p>
 <p>
  <strong>
   Department:
  </strong>
  R&amp;D &ndash; Process Development
 </p>
 <p>
  <strong>
   Industry:
  </strong>
  CDMO / API
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Purpose of the Role:
  </strong>
 </p>
 <p>
  To lead and execute the development, optimization, and scale-up of robust, cost-effective, and regulatory-compliant chemical processes for Active Pharmaceutical Ingredients (APIs) and intermediates, ensuring smooth technology transfer from lab to kilo lab and manufacturing.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <p>
  <strong>
   1. Strategic Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Drive innovation by designing synthetic routes that align with project timelines and regulatory requirements.
  </li>
  <li>
   Contribute to technology differentiation strategies that enhance the CDMO&rsquo;s scientific credibility and client value proposition.
  </li>
  <li>
   Collaborate with cross-functional teams (Analytical, QA/QC, Regulatory) to support integrated drug development solutions.
  </li>
 </ul>
 <p>
  <strong>
   2. Operational Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Perform route scouting, literature search, and develop robust and scalable chemical processes using QbD principles.
  </li>
  <li>
   Conduct laboratory experiments for reaction optimization, impurity profiling, and process safety assessment.
  </li>
  <li>
   Prepare and review technical reports, SOPs, and technology transfer documents.
  </li>
  <li>
   Ensure compliance with GMP/GLP and EHS standards during lab-scale and pilot-scale operations.
  </li>
  <li>
   Participate in troubleshooting during scale-up or commercial production batches and provide technical support during client audits.
  </li>
 </ul>
 <p>
  <strong>
   3. Financial Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Optimize process economics by reducing cycle time, yield improvement, and minimizing raw material costs.
  </li>
  <li>
   Support cost estimation activities during project proposals or client RFQs by providing technical insights.
  </li>
 </ul>
 <p>
  <strong>
   4. People &amp; Collaboration Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Guide junior team members on experimental planning, data interpretation, and documentation best practices.
  </li>
  <li>
   Promote a culture of safety, learning, and innovation within the team.
  </li>
  <li>
   Work closely with Program Management and Business Development to align project goals with customer expectations.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications &amp; Experience
  </strong>
 </p>
 <ul>
  <li>
   M.Sc ( Organic Chemistry)
  </li>
  <li>
   3&ndash;9 years of experience in Process R&amp;D, preferably in CDMO organizations
  </li>
  <li>
   Hands-on expertise in synthesis, scale-up, impurity profiling, and technology transfer
  </li>
  <li>
   Familiarity with analytical techniques (HPLC, GC, NMR) and regulatory documentation
  </li>
 </ul>
 <p>
 </p>
</div>


Exact Sciences

<div><p><b>Help us change lives</b></p><p>
At Exact Sciences, we&rsquo;re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you&rsquo;re working to help others.</p><p></p><p><b>
Position Overview</b></p><p>
The Research Scientist, with limited guidance from more experienced scientists, works individually and in collaboration with others on multiple projects which are moderate to complex in scope. The Research Scientist plays an active role in planning of projects and experiments and is often the technical lead responsible for the successful execution of the project. This position involves independently making detailed observations, analyzing data and interpreting results. Working in a team setting, the Research Scientist, will primarily be involved in Research and Development projects serving as a technical lead in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products.</p><p></p><p><b>
Essential Duties</b></p><p>
include but are not limited to the following:</p><ul><li>
Conduct bench level experiments within several product or technology areas and identify problems and discrepancies.</li><li>
Independently plan and analyze results of bench level experiments within several product or technology areas; effectively present at data meetings, group meetings, and project team meetings.</li><li>
Operate scientific instrumentation related to performance of duties and notify appropriate personnel of any problems.</li><li>
Effectively utilize and apply methods or technologies and provide ideas for new techniques, when appropriate.</li><li>
Maintain knowledge of technological industry developments that could assist in completion of an assignment or aid in the development of new processes or procedures.</li><li>
Provide technical input and participate in decisions affecting project planning and experimental design.</li><li>
Prepare and provide information and data for scientific abstracts/conferences/project meetings/publication.</li><li>
Generate, document, and communicate development plans for critical aspects of a project.</li><li>
Participate in the development of research plans and experimental outlines, write experimental protocols, and perform laboratory experiments.</li><li>
Prepare detailed technical procedures, protocols, and reports.</li><li>
Evaluate impact of nonconforming data to product or process.</li><li>
Identify and address trends in study data.</li><li>
Prepare and approve written reports.</li><li>
Lead identification of areas for process improvements.</li><li>
Maintain lab notebook in a complete and consistent manner, following all legal, ISO, and QSR requirements, as well as keeping clear and complete.</li><li>
Prepare reports and documentation providing the analysis or summarization of experimental results, outcomes, and next steps to supervisor, technical teams/groups, or project teams.</li><li>
Present experimental results and defend scientific ideas and findings at project or departmental meetings; provide technical input, as needed.</li><li>
Work on problems of diverse and complex in scope in which analysis of data requires evaluation of identifiable factors.</li><li>
Exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.</li><li>
Work on individual assignments and with project team members, as appropriate, to meet department and project objectives.</li><li>
Work within project timeframes that are established collaboratively by team members.</li><li>
Act as technical leader for one or more projects that are moderate to complex in scope.</li><li>
Exercise discretion and independent judgement within broadly defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining and interpreting results, analyzing data, and presenting findings in a professional and knowledgeable manner.</li><li>
Promote an open, collaborative environment built on trust to foster positive teamwork.</li><li>
Assist in planning and recommendation of activities that account for prioritization of organizational and department goals.</li><li>
Ability to train and mentor research associates.</li><li>
Ability to organize, present, and convey moderate problems or issues.</li><li>
Ability to communicate clearly with supervisor and group members.</li><li>
Excellent presentation skills.</li><li>
Ability to collaborate, work effectively and contribute within team, department, and cross-functional teams.</li><li>
Strong attention to detail skills.</li><li>
Ability to effectively work on several varied projects at one time, with frequent changing priorities.</li><li>
Excellent analytical, problem solving, and decision-making skills.</li><li>
Apply technical knowledge, scientific creativity and rigor, collaboration with others, and independent thought; ability to provide insights and defend scientific ideas.</li><li>
Apply experimental knowledge and outcomes to new and valuable problems; ability to make predictions based on a deep understanding of the fundamental nature of the inputs into a decision or action.</li><li>
Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.</li><li>
Support and comply with the company&rsquo;s Quality Management System policies and procedures.</li><li>
Regular and reliable attendance.</li><li>
Ability to lift up to 20 pounds for approximately 5% of a typical working day.</li><li>
Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 50% of a typical working day.</li><li>
Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height.</li><li>
Ability to comply with any applicable personal protective equipment requirements.</li><li>
Ability to use various types of laboratory equipment including microscopes, microtomes, blades, strainers, and pipettes for extended periods of time.</li><li>
May perform repetitious actions using lab tools.</li><li>
Ability to use near vision to view samples at close range.</li><li>
May be exposed to hazardous materials, tissue specimens and instruments with moving parts, lasers, heating and freezing elements, and high-speed centrifugation.</li><li>
Ability and means to travel between local Exact Sciences locations.</li><li>
Ability to travel 5% of working time away from work location, may include overnight/weekend travel.</li></ul><p></p><p><b>
Minimum Qualifications</b></p><ul><li>
PhD in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or related field; or Master&rsquo;s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or related field and 4 years of related experience in lieu of a PhD; or Bachelor&rsquo;s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or related field and 6 years of related experience in lieu of PhD.</li><li>
1+ years of experience in medical device/IVD, biotech, life science, or pharmaceutical industry.</li><li>
Demonstrated ability to apply molecular biology and/or biochemical techniques.</li><li>
Demonstrated understanding of GMP, ISO, and Quality Systems.</li><li>
Good knowledge of molecular biology and/or biochemistry and/or next-generation sequencing (NGS) and genomics.</li><li>
Basic knowledge of statistical and mathematical methods in biology/genetics/genomics; including experience with statistical software, such as JMP</li><li>
Proficient computer skills to include Internet navigation, Email usage, and word processing.</li><li>
Proficient in Microsoft Office to include Excel, Word, and PowerPoint.</li><li>
Demonstrated ability to perform the Essential Duties of the position with or without accommodation.</li><li>
Authorization to work in the United States without sponsorship.</li></ul><p></p>
#LI-TA21<p></p><p>
Salary Range:</p>
$89,000.00 - $151,000.00<br>
<p></p>
The annual base salary shown is for this position located in US - WI - Madison on a full-time basis. In addition, this position is bonus eligible.<p></p><p>
Exact Sciences is proud to offer an employee experience that includes paid time off (including days for vacation, holidays, volunteering, and personal time), paid leave for parents and caregivers, a retirement savings plan, wellness support, and health benefits including medical, prescription drug, dental, and vision coverage. Learn more about our benefits.</p><p></p><p>
Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, please contact us here.</p><p></p><p>
Not ready to apply? Join our Talent Community to stay updated on the latest news and opportunities at Exact Sciences.</p><p></p><p>
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to disability, protected veteran status, and any other status protected by applicable local, state, or federal law.</p><p></p><p>
To view the Right to Work, E-Verify Employer, and Pay Transparency notices and Federal, Federal Contractor, and State employment law posters, visit our compliance hub. The documents summarize important details of the law and provide key points that you have a right to know.</p></div>

UT Health Science Center at San Antonio

<div><p>Job Description</p></div>
<br><div><p>Responsible for planning, designing, monitoring, coordinating, analyzing and producing scientific content for clinical and regulatory documents. Manages and reviews medical writing of study protocols, statistical analysis and study reports.</p></div>
<br><div><ul>Responsibilities</ul></div>
<br><div><ul><li>Develops, designs, and executes large and complex research projects, reviews progress, analyses data and evaluates results.
</li><li>Formulates research methods and suggests options for improving quality; identifies potential problems and recommends and implements solutions.
</li><li>Consults with users to refine or adapt methodologies to fit research requirements; collaborates in development of new techniques and instruments.
</li><li>Organizes, maintains the laboratory, researches and recommends equipment and maintains documentation and storage of biomaterials.
</li><li>Co-authors/authors scientific publications; presents at meetings and conferences; participates in acquiring research funding including writing grant proposals.
</li><li>Manages and reviews medical writing of study protocols, statistical analysis and study reports.
</li><li>Performs all other duties as assigned.</li></ul></div>
<br><p></p><div>Qualifications</div>
<br><div><ul><li>Demonstrated ability to organize and coordinate work within schedule constraints and handle emergent requirements in a timely manner.
</li><li>Demonstrated ability to monitor important and complex projects concurrently.
</li><li>Knowledge of Microsoft Word, Excel, PowerPoint, and Lotus Notes/other email software.
</li><li>Demonstrated ability to effectively communicate verbally and in writing, to include writing and preparing memorandums, letters, and other official correspondence.
</li></ul><p>EDUCATION:
</p><ul><li>Master's degree in related field is required.
</li></ul><p>EXPERIENCE:
</p><ul><li>Two (2) years of related experience is required.</li></ul></div>
<br>Required Skills
<br>Two (2) years of related experience is required.

SRM Institute of Science and Technology

<p>&#9679; Delegated duties of the clinical trials</p><p>&#9679; Maintenance of the trial master files</p><p>&#9679; Involved in the consent process and documentation</p><p>&#9679; Randomization and allocation, Electronic data capture</p><p>&#9679; Prepare the documents for SAE reporting, if any</p><p>&#9679; Reviewing scientific literature and attending conferences to stay current with advances in clinical research</p><p>&#9679; Preparing reports on study results and submitting them to colleagues and supervisors</p><p>&#9679; Reviewing data from clinical trials to ensure that study procedures were followed accurately</p><p>&#9679; Coming up with new ideas for research projects that can be conducted within the department or company</p><p>&#9679; Participating in research projects related to pharmacokinetics and pharmacodynamics</p><p>&#9679; Preparing publications, presentations or working reports; and</p><p>&#9679; Performing other research and administrative duties as assigned</p><p>&#9679; Participate with the PI and study team to identify and prioritize the development of systems and infrastructure to maintain research quality and compliance</p><p>Occasional travel to attend sponsor study training meetings as required</p><p>Job Type: Full-time</p><p>Pay: &#8377;70,000.00 - &#8377;72,000.00 per month</p>

Search 8135+ Research scientist jobs near you this September. New roles added regularly across leading industries. Apply today.

8135 research scientist jobs NEAR_ME

Research Scientist ( 82209156 )

Research Scientist

Research Scientist

Research Scientist

Research Scientist

Research Scientist

Research Scientist