8,398 Research And Development Scientist jobs in India

Provide training in Precession Electron Diffraction & TEM applications (Orientation/Phase mapping, Crystallography), support Raman Spectroscopy analysis, and research scientific journals & papers.

Job Title: Project Associate – Process Research (R&D)

Department: Research & Development – Process Research

Location: Jamshedpur

Employment Type: Fixed Term Contract (FTC) – 3 Years

Annual CTC: ₹3 LPA + Company Benefits

About the Role

We are looking for a motivated and skilled Project Associate to join our Process Research team in R&D . The ideal candidate should have a strong foundation in Chemistry with hands-on experience in laboratory experimentation and data analysis. The role will involve experimental research, catalyst analysis, process development, and technical documentation .

Key Responsibilities

• Conduct laboratory experiments related to process research and development.
• Work on catalyst preparation, characterization, and performance studies.
• Collect, analyze, and interpret experimental data.
• Maintain detailed experimental records and prepare technical reports.
• Support ongoing R&D projects and assist senior scientists in process scale-up activities.
• Prepare technical papers and patent drafts as required.
• Ensure adherence to safety and quality standards in the laboratory.
• Collaborate cross-functionally within R&D and production teams.

Required Qualifications

• Education: Full-time M.Sc. in Chemistry (Organic/Inorganic/Physical/Analytical preferred).
• Experience: Minimum 1 year of relevant industrial or academic research experience .

Skills & Competencies

• Strong experimental and analytical skills .
• Understanding of catalyst chemistry/process chemistry .
• Proficiency in MS Office (Excel, Word, Teams, Calendar).
• Ability to analyze data and create technical documentation.
• Exposure to technical paper or patent writing is an added advantage.
• Good problem-solving skills and attention to detail.
• Effective communication and teamwork abilities.

Company Benefits

• Competitive salary
• Health and insurance benefits
• Training and development opportunities
• Work-life balance and professional growth environment

About CLPS RiDiK

RiDiK is a global technology solutions provider and a subsidiary of CLPS Incorporation (NASDAQ: CLPS), delivering cutting-edge end-to-end services across banking, wealth management, and e-commerce. With deep expertise in AI, cloud, big data, and blockchain, we support clients across Asia, North America, and the Middle East in driving digital transformation and achieving sustainable growth. Operating from regional hubs in 10 countries and backed by a global delivery network, we combine local insight with technical excellence to deliver real, measurable impact. Join RiDiK and be part of an innovative, fast-growing team shaping the future of technology across industries.

Find your next role with MedGenome Labs Ltd. We are the market leader in clinical genomic space in India and offers a comprehensive rangeof diagnostic servicesto doctors and researchers. We operate the largest CAP accredited Next Generation Sequencing (NGS) lab in Southeast Asia housing cutting-edge genome sequencing platforms. MedGenome is the founding member of GenomeAsia 100K, an initiative to sequence 100,000 Genomes in Asia.

We have an exciting opportunity for the position of Research Associate in New Delhi location. It is a full time and work from office opportunity.

Skills and Experience Required:

• 2+ years of experience in Extraction of nucleic acids (DNA/RNA) from biological materials including prenatal samples
• Performing QC for nucleic acids
• Processing samples for fragment analysis based tests – MCC and Aneuploidy (QF-PCR) & repeat nucleotide disorders.
• Processing samples for Sanger (Single variant & Prenatal) and MLPA based tests.
• Analysis, interpretation and reporting for MCC, QF-PCR, Sanger & MLPA data.
• Processing samples for NGS libraries and sequencing.
• Updating LIMS & MIS properly to ensure seamless workflow.
• Maintaining inventory while giving timely updates and ensuring the lab is in order
• Ensuring documentation of worksheets and methodical filling of all log sheets which include instrument log sheets and process related google sheets.
• Coordinating with the managers for sample processing, QC checks, documentations and maintaining turnaround time in each step of the process
• Taking part in CAP and other accreditation affairs. Follow CAP related activities and CAP compliance in the workplace
• Strictly adhere to lab Quality Processes and follow Standard Operating Procedures (SOPs)
• Training new joiners in Standard Operating Procedures (SOPs) and lab workflows
• Maintain cordial working relationship with everyone in the company
• Test optimization where required and any other responsibilities assigned by the Manager/Company.
• Maintaining a cordial working relationship with everyone in the company

Educational Qualification:

Masters in Human Genetics or Biotechnology or relevant studies.

If you are interested in this position, please click the APPLY NOW button for immediate employment consideration. We regret that due to volume of response, we can only contact initial successful applicants. If you have not heard from us within 7 days, then your application has been unsuccessful.

About Atomgrid

Atomgrid is a global platform for sourcing and contract manufacturing of specialty chemicals from India. Our vision is to revolutionize the global specialty chemicals industry through cutting-edge technology, relentless innovation, and impeccable execution.

We work with our customers right from lab-scale development to commercial scale-up and doorstep delivery for their strategic procurement projects. Our in-house team of scientists, technology engineers, and project managers ensures the right quality products are delivered at the right price and on time.

We are founded by IIT & IIM founders and backed by marquee VCs in India.

Position: Research And Development Associate - Analytical

Location: Bengaluru, Karnataka

Qualification: M.Sc. / B.Sc. in Organic Chemistry

Job Overview

We are looking for a Process Development Chemist (Testing & Analytical Focus) to ensure all developed processes and products are validated through robust analytical testing. You will work closely with the R&D and process teams, conducting key evaluations such as cloud point, saponification value, Gardner color, pH, acid value, viscosity, and related performance tests.

This role is ideal for someone detail-oriented, analytical, and passionate about bridging process chemistry with validation and quality assurance.

Requirements

• 1–3 years of laboratory experience in surfactants or emulsifiers testing
• Exposure to QC, QA, or analytical labs in chemical plants is preferred
• Hands-on knowledge of testing methods (cloud point, acid value, viscosity, etc.)
• Familiarity with analytical instruments (GC, HPLC, FTIR, UV-Vis) is a plus
• Strong documentation, data analysis, and teamwork skills

Roles and Responsibilities

• Conduct routine and advanced analytical testing on surfactant and emulsifier samples.
• Evaluate parameters like cloud point, saponification value, color, pH, viscosity, and moisture
• Support process validation and scale-up by comparing analytical results across lab → pilot → plant stages.
• Maintain accurate test records and prepare reports, data sheets, and compliance documentation.
• Ensure strict adherence to GLP and safety protocols.
• Collaborate with process chemists and other teams for troubleshooting and optimization.

Why Join Us?

• Opportunity to specialize in analytical testing within process development.
• Exposure to cutting-edge R&D projects in surfactants and specialty chemicals.
• Clear growth path into Analytical Scientist / QC Lead roles.
• Collaborative, innovation-driven environment that values accuracy, learning, and ownership.

• Design and conduct experiments to identify and validate novel drug targets.
• Synthesize and characterize potential drug candidates using advanced chemical techniques.
• Evaluate the efficacy and safety of compounds in preclinical models.
• Collaborate with cross-functional teams, including biologists, pharmacologists, and toxicologists, to advance drug candidates through the pipeline.
• Analyze experimental data, interpret results, and present findings at internal and external scientific meetings.
• Contribute to the preparation of regulatory submissions and patent applications.
• Maintain detailed laboratory notebooks and ensure compliance with Good Laboratory Practices (GLP).
• Stay abreast of the latest scientific literature and technological advancements in the pharmaceutical field.
• Mentor junior scientists and research assistants.
• Troubleshoot experimental issues and optimize protocols.

• Ph.D. in Medicinal Chemistry, Pharmacology, Biochemistry, or a closely related field.
• Minimum of 3-5 years of postdoctoral or industry research experience in drug discovery.
• Demonstrated expertise in organic synthesis, assay development, and in vitro/in vivo pharmacology.
• Strong understanding of molecular biology, cell biology, and disease mechanisms.
• Experience with analytical techniques such as HPLC, LC-MS, and NMR.
• Excellent written and verbal communication skills, with a track record of publications in peer-reviewed journals.
• Ability to manage multiple projects simultaneously and work effectively in a fast-paced environment.
• Proficiency in data analysis software.
• Experience with regulatory affairs is a plus.
• A proactive approach to problem-solving and a commitment to scientific rigor.

• Design and conduct laboratory experiments to support pharmaceutical research and development projects.
• Investigate, develop, and optimize synthetic routes for novel drug candidates.
• Develop and validate analytical methods for characterizing drug substances and formulations.
• Perform in-vitro and in-vivo studies to assess drug efficacy and safety profiles.
• Analyze experimental data, interpret results, and contribute to scientific reports and publications.
• Collaborate with cross-functional teams, including biologists, pharmacologists, and toxicologists.
• Stay current with scientific literature and emerging technologies in pharmaceutical sciences.
• Maintain accurate and detailed laboratory notebooks and documentation.
• Contribute to intellectual property generation through patent filings.
• Ensure compliance with laboratory safety protocols and regulatory guidelines (e.g., GLP, GMP).
• Mentor junior research associates and interns.

• Ph.D. in Pharmaceutical Sciences, Medicinal Chemistry, Organic Chemistry, Analytical Chemistry, or a related discipline.
• Minimum of 3 years of post-doctoral or industry research experience in pharmaceutical R&D.
• Proven expertise in at least one of the following areas: small molecule synthesis, formulation development, analytical method development (HPLC, GC-MS), or preclinical drug testing.
• Proficiency in relevant laboratory techniques and instrumentation.
• Strong understanding of drug discovery and development processes.
• Excellent problem-solving skills and ability to think critically.
• Strong written and verbal communication skills, with a track record of scientific presentations and publications.
• Ability to work independently and collaboratively in a team-oriented research environment.
• Proficiency in scientific data analysis software.
• Experience with regulatory guidelines in the pharmaceutical industry is a plus.

• Design, execute, and interpret complex research experiments.
• Lead drug discovery and development projects from concept to completion.
• Develop and validate novel in vitro and in vivo assays.
• Analyze and troubleshoot experimental data, identifying key findings and implications.
• Collaborate with interdisciplinary teams to advance drug candidates.
• Mentor and guide junior research staff.
• Prepare comprehensive research reports and scientific publications.
• Present research findings to scientific advisory boards and stakeholders.
• Stay current with emerging scientific literature and technological advancements.
• Contribute to the strategic planning of research programs.
• Ensure compliance with all safety and ethical guidelines in research.

• Lead independent research projects in drug discovery and development.
• Design, execute, and analyze complex preclinical experiments.
• Develop and validate novel assays and screening methodologies.
• Explore and validate new therapeutic targets and pathways.
• Optimize lead compounds for pharmacokinetic and pharmacodynamic properties.
• Interpret experimental data and present findings to scientific teams.
• Contribute to the preparation of research reports, publications, and patents.
• Mentor and guide junior research scientists.
• Collaborate with internal and external stakeholders.
• Stay current with scientific literature and technological advancements in the field.

• PhD in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
• Minimum of 7 years of post-doctoral research experience in the pharmaceutical industry or a leading research institution.
• Proven track record of successfully advancing drug candidates through preclinical development.
• Extensive experience in assay development, in vitro and in vivo pharmacology studies.
• Strong knowledge of medicinal chemistry principles and drug metabolism.
• Proficiency with advanced analytical and molecular biology techniques.
• Excellent data analysis, interpretation, and presentation skills.
• Demonstrated ability to lead research projects and mentor junior staff.
• Strong communication and collaboration skills.
• Experience in a hybrid work environment.