6,723 Analytical Scientist jobs in India

Our client is seeking a highly accomplished and visionary Principal Scientist specializing in Analytical Chemistry. This role is crucial for leading advanced research and development initiatives, driving innovation, and setting the scientific direction within our R&D department. You will be responsible for designing and executing complex analytical experiments, developing and validating novel analytical methodologies, and interpreting intricate data sets. Key responsibilities include troubleshooting analytical challenges, providing expert guidance on instrumental techniques, and contributing to the intellectual property portfolio. You will collaborate closely with cross-functional teams, including formulation scientists, process engineers, and regulatory affairs specialists, to support product development and ensure quality control. The ideal candidate will possess a Ph.D. in Analytical Chemistry or a closely related field, with extensive experience in pharmaceutical, chemical, or a similar scientific industry. Demonstrated expertise in a wide range of analytical techniques (e.g., HPLC, GC, Mass Spectrometry, NMR, spectroscopy) is essential. Strong leadership, mentorship, and communication skills are paramount, as you will guide junior scientists and present findings to diverse audiences. A track record of successful scientific publications and a deep understanding of scientific rigor are highly valued. This position offers the flexibility of remote work, allowing you to contribute your expertise from a dedicated home laboratory or office space. We are committed to fostering an environment of scientific excellence and encourage groundbreaking research. This is an unparalleled opportunity for an experienced scientist to make a significant impact on scientific discovery and innovation. The job is based in Ahmedabad, Gujarat, IN, but is fully remote.

Our client, a leading firm in Scientific Research & Development, is seeking a highly accomplished Principal Scientist specializing in Analytical Chemistry to join their state-of-the-art facility in Vadodara, Gujarat, IN . This senior role will involve leading complex analytical projects, developing innovative methodologies, and contributing to cutting-edge research initiatives. The Principal Scientist will be responsible for designing and executing experiments, interpreting sophisticated analytical data, and ensuring the highest standards of scientific rigor and quality. You will utilize a wide range of advanced analytical techniques and instrumentation, including chromatography (HPLC, GC), spectroscopy (MS, NMR, UV-Vis), and thermal analysis. Key responsibilities include supervising and mentoring junior scientists and technicians, managing laboratory resources, staying abreast of the latest scientific advancements, and publishing research findings in peer-reviewed journals. A deep expertise in method development, validation, and troubleshooting is essential. The ideal candidate will possess a Ph.D. in Analytical Chemistry or a closely related field, with a minimum of 10 years of post-doctoral research experience in an industrial or academic setting. Excellent written and verbal communication skills, strong leadership abilities, and a passion for scientific discovery are critical. This is a unique opportunity to lead impactful research, contribute to significant scientific advancements, and drive innovation within a collaborative and research-intensive environment.

Our client is seeking an accomplished Principal Scientist specializing in Analytical Chemistry to lead groundbreaking research and development initiatives in Ahmedabad, Gujarat, IN . This senior role will be instrumental in developing and validating state-of-the-art analytical methodologies to support product characterization, quality control, and troubleshooting across various scientific domains. The ideal candidate will possess deep expertise in a range of analytical techniques, including chromatography (HPLC, GC), mass spectrometry (MS), spectroscopy (UV-Vis, IR, NMR), and hyphenated techniques. You will be responsible for designing complex analytical studies, interpreting sophisticated data sets, and developing robust, validated methods in compliance with relevant industry standards (e.g., GLP, GMP). Key responsibilities include leading analytical projects, mentoring junior scientists, and collaborating closely with cross-functional teams, including formulation, process development, and quality assurance. The Principal Scientist will contribute to the strategic direction of the analytical department, staying abreast of emerging technologies and recommending their adoption. Troubleshooting complex analytical challenges and developing innovative solutions will be a critical aspect of the role. Experience in method development and validation for diverse matrices and complex samples is essential. The candidate will also be expected to author and review technical reports, scientific publications, and contribute to regulatory filings. A Ph.D. in Analytical Chemistry, Biochemistry, or a closely related field, with a minimum of 7 years of post-doctoral research or industry experience, is required. Strong leadership capabilities, excellent scientific communication skills, and a proven track record of independent research and problem-solving are paramount. This is an exceptional opportunity to make a significant impact in a leading scientific organization.

Our client is seeking a highly accomplished Principal Scientist specializing in Analytical Chemistry to lead critical research and development initiatives in Patna, Bihar, IN . This senior role is essential for driving innovation, developing new analytical methodologies, and ensuring the highest standards of quality and precision in scientific research. The ideal candidate will possess a Ph.D. in Analytical Chemistry or a closely related field, with a substantial track record of scientific achievement, publications, and project leadership. You will be responsible for designing and executing complex analytical experiments, utilizing state-of-the-art instrumentation and techniques, such as chromatography (HPLC, GC), mass spectrometry (MS), spectroscopy (UV-Vis, IR, NMR), and thermal analysis. Key responsibilities include method development, validation, and transfer for various applications, ensuring robustness and accuracy. You will lead a team of analytical chemists, providing technical guidance, mentorship, and fostering a collaborative research environment. This position demands exceptional problem-solving skills, a meticulous approach to data analysis, and the ability to interpret results to draw meaningful conclusions. You will collaborate closely with R&D teams, product development, and quality assurance departments to support project goals and regulatory compliance. Experience with pharmaceutical analysis, environmental testing, or materials science is highly advantageous. The ability to manage multiple projects simultaneously, secure funding through grant proposals, and present scientific findings at conferences and in publications is crucial. This is a challenging and rewarding opportunity to contribute to groundbreaking scientific advancements and lead a dedicated team of scientists in a cutting-edge research setting.
Responsibilities:

• Lead analytical chemistry research and development projects.
• Develop, validate, and optimize analytical methods using various techniques (HPLC, GC, MS, Spectroscopy).
• Oversee the operation and maintenance of advanced analytical instrumentation.
• Interpret complex analytical data and provide insightful conclusions.
• Troubleshoot analytical issues and implement solutions.
• Mentor and guide junior scientists and technicians.
• Collaborate with cross-functional teams to support R&D and product development.
• Ensure compliance with quality control and regulatory standards.
• Stay abreast of new analytical technologies and methodologies.
• Prepare technical reports, publications, and presentations.
• Contribute to the strategic direction of the R&D department.

Qualifications:

• Ph.D. in Analytical Chemistry or a related scientific discipline.
• 8+ years of experience in analytical chemistry, with a strong focus on method development and validation.
• Extensive hands-on experience with a wide range of analytical instruments (e.g., HPLC, GC-MS, NMR, ICP-MS).
• Proven ability to interpret complex analytical data and solve challenging scientific problems.
• Experience in leading scientific projects and mentoring research teams.
• Strong understanding of Good Laboratory Practices (GLP) and regulatory requirements.
• Excellent written and verbal communication skills.
• Ability to work independently and collaboratively in a team environment.
• Experience in pharmaceutical analysis, environmental science, or materials characterization is a plus.
• Demonstrated publication record in peer-reviewed journals.

Our client, a leading pharmaceutical research and manufacturing organization, is looking for a dedicated Senior Analytical Development Scientist to join their quality control and assurance team in Mysuru, Karnataka, IN . This critical role involves the development, validation, and implementation of advanced analytical methods for raw materials, in-process samples, and finished pharmaceutical products. The ideal candidate will possess a deep understanding of analytical chemistry principles and techniques, including HPLC, GC, MS, UV-Vis, FT-IR, and dissolution testing. You will be responsible for troubleshooting analytical methods, investigating out-of-specification (OOS) results, and ensuring compliance with regulatory guidelines (e.g., ICH, FDA, EMA). Key responsibilities include leading method development projects, optimizing existing analytical procedures, preparing and reviewing validation protocols and reports, and collaborating with R&D and manufacturing departments. Experience with stability studies and extractables/leachables testing is highly desirable. A Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmacy, or a related scientific discipline, with a minimum of 6 years of experience in pharmaceutical analytical development, is required. A Ph.D. is a plus. Strong scientific curiosity, meticulous attention to detail, and excellent problem-solving skills are essential. You will work in a well-equipped laboratory environment and contribute to ensuring the quality and safety of our client's pharmaceutical products. This is an excellent opportunity to advance your career in analytical sciences within a reputable pharmaceutical company.

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.

**Description**
At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds-regardless of background-to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
**Brief Job Overview**
This is a non-supervisory position to support process development and scale-up of Active Pharmaceutical Ingredient (API) and related materials. The successful applicant in this role will work on projects including Analytical Method Development and evaluation for in-process samples for synthetic chemistry. The successful candidate will also perform a variety of non-routine and routine analytical tests, maintains safety & GLP environment in the lab including development/validation of methods, stability studies and research projects in analytical chemistry. The successful applicant will direct, troubleshoot, and share insights on complex projects while drawing independent conclusions about the results and determining how to proceed with the project. They closely collaborate with other scientists and/or other USP personnel.
**How will YOU create impact here at USP?**
As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.
Additionally, USP's People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.
The Scientist IV has the following responsibilities:
+ Support reaction monitoring, scale-up and final analysis of samples as per monograph /in-house procedures including method development/validation if required. Prepare development reports for Synthetic Support projects. Execute projects per the approved test protocols if assigned.
+ In collaboration with the synthetics team evaluate, implement and grow Process Analytical Technologies (PAT) capabilities and expertise. This includes evaluation of process monitoring, understanding, and control via in line, online and at line techniques. Serve as technical expert and champion for PAT and/or process model building.
+ Plan, execute, and complete the projects as per specifications, timelines, and budget.
+ Responsible for preparation and review of SOPs, protocols, reports, etc.
+ Ensure project requirements by coordinating with external vendors and all internal relevant departments.
+ Responsible for ensuring the required maintenance and calibrations of the equipment
+ Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned
+ Preparation and planning for ISO-9001 certification/recertification by participating actively, verification of protocols and related documents and take an active role in the internal as well as external QA audits and address the audit issues in a timely manner.
+ Maintain GLP & implement safety procedures while working in Lab.
+ Work on any other assigned tasks/ lab management activities.
+ Conversant with lab safety norms and strictly follow them.
+ Collaborate within the team and cross functional teams
+ Learn and practice Diversity, Equity, Inclusion & Belonging culture
**Who is USP Looking For?**
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
+ MSc. in Analytical Chemistry / Organic Chemistry/M. Pharm, having 8-10 years of experience in Analytical Research and Development or Ph.D. with 4-7 years of experience in Analytical Research and Development.
+ Must have hands on experience in working with chemical methods and handling instruments like HPLC, GC, LC-MS, GC-MS, FTIR, UV-Visible, wet chemistry, etc.
+ Understanding of process analytical technology, chemometrics, and knowledge of in-line, online, at line process analytical tools (e.g., IR, Raman, HPLC)
+ Experience in analytical testing and development with focus on process analytical chemistry and to understand, monitor and control chemical processes/reactions.
+ A comprehensive understanding of the science involved in the development of synthetic organic molecules and analytical chemistry.
+ Ability to perform analytical method developments and method validations as and when required.
+ Excellent technical writing and verbal communication skills
+ Good interpersonal skills and proven ability to function in a team-oriented environment are necessary.
We especially welcome applications from those who hold historically marginalized and/or underrepresented identities. This job description provides a portrait of an ideal candidate. Candidates who possess many, though perhaps not all, qualifications are encouraged to apply.
**Additional Desired Preferences**
+ Hands on experience with PAT instruments, techniques, and models such as in line, at line, or online IR, Raman, HPLC, NMR, etc.
+ Experience with a wide variety of software and laboratory information systems, including chemometric modeling software
+ Working knowledge of API manufacturing and product testing (e.g. ICH guidelines, USP general chapters and monographs)
+ Expertise with USP compendial methods and requirements (e.g. monographs and general chapter) and ICH quality guidelines
+ Pharmaceutical laboratory experience, method development and method implementation in manufacturing environments, and/or continuous manufacturing experience.
+ Strong project management skills with ability to be effective both independently and in collaborative teams
+ Skilled in evaluation and interpretation of data; Ability to multi-task.
+ Skilled in anticipating, troubleshooting, and solving technical problems.
+ Takes personal responsibility to ensure work is delivered on time and is of the highest quality.
**Supervisory Responsibilities**
NA
**Benefits**
USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
**Job Category** Chemistry & Scientific Standards
**Job Type** Full-Time

**Description**
At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds-regardless of background-to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
**Brief Job Overview**
This is a supervisory position in USP-India's NMR Laboratory. In this role, the Senior scientist-II works on projects including Characterization of molecules for synthetic chemistry, CDL and reference standard/ General Chapter development for Biologics and Verification Labs. The successful candidate will review/monitor a variety of non-routine and routine NMR tests, maintains safety & GLP environment in the lab including evaluation of reference standards, development/validation (as per requirement) of official methods, stability studies, and research projects in NMR department.
**How will YOU create impact here at USP?**
As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.
Additionally, USP's People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.
The Sr. Scientist II, TL has the following responsibilities:
+ (70%) Review NMR sample analysis reports as per monograph / in-house procedures including reaction monitoring. Prepare NMR reports, involve in project acceptance & approvals. Ensure the project's requirement by coordinating with the purchase department. Coordinate with lab scientists to complete projects within timelines. Prepare/review lab reports and documents.
+ (10%) Ensure that the calibrations of the equipment's are performed as per the schedule.
Prepare, Execute and complete IQ/OQ/PQ of new instruments. Indent the required glass ware and chemicals for the NMR projects. Maintain GLP & implement safety procedures
while working in Lab. Perform additional Projects/activities as per the requirement.
+ (10%) Assist in the development and implementation of safety projects impacting all USP Laboratory personnel. Participates in USP cross-functional teams as appropriate. Develop Standard Operating Procedures and policies in NMR Lab. Coordinate with Quality Assurance staff to ensure the implementation of corrective actions. Responsible for internal, method, ISO-9001 & ISO-17025 audits
+ (10%) Promote Diversity, Equity, Inclusion, and Belonging principles at USP India.
**Who is USP Looking For?**
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
+ MSc. in Analytical Chemistry / Organic Chemistry/ M. Pharm, having 13-15 years' experience in NMR or Ph.D. with 10-13 years of experience in NMR.
+ Must have hands on experience in handling NMR instruments.
+ Proficient in small molecule structure elucidation using NMR. Exposure to GMP/GLP environment and documentation procedures required.
+ Expertise with Bruker NMR software- automation software & hardware including cryo-probes.
+ Knowledge of solid state NMR and multinuclear NMR operations.
+ A comprehensive understanding of the science involved in the development of synthetic organic molecules and analytical chemistry.
+ Must be able to communicate effectively with both internal and external customers. Preferably familiar with electronic notebook documentation of experimental procedures.
+ Must possess a strong work ethic and a solid record of problem solving and technical results.
Excellent technical writing and verbal communication skills are required.
+ Good interpersonal skills and proven ability to function in a team-oriented environment are necessary. Proven self-effectiveness skills are a must. Understanding of GMP / ISO-IEC 17025 Guidelines is a requirement
+ Effective coach and mentor to staff. Ability to identify and develop talent.
+ Demonstrated stakeholder collaboration experience, with the ability to quickly develop and manage internal and external relationships and contacts.
**- Ability to lead in a fast paced environment with changing deadlines and priorities.**
**Additional Desired Preferences**
Desired preferences are to showcase any additional preferred levels of expertise to perform the role. Reminder: any items listed in this section are not requirements nor disqualifies for candidate consideration.
+ Experience on biological molecules such as peptides, proteins and vaccines would be an added advantage.
+ General chapter information, ELN, Empower and NuGenesis will be an added advantage.
+ Skilled in evaluation and interpretation of data; Ability to multi-task.
+ Skilled in anticipating, troubleshooting, and solving technical problems.
+ Takes personal responsibility to ensure work is delivered on time and is of the highest quality.
**Supervisory Responsibilities**
Six direct reports. TA, Scientist-I, Scientist-II, Scientist-III and two Scientist-IV
**Benefits**
USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
**Job Category** Chemistry & Scientific Standards
**Job Type** Full-Time