10,911 Research Assistants jobs in India

The Research Support Intern will provide end-to-end assistance to researchers, scholars, and clients by offering high-quality support in literature search, data organization, reference management, and formatting. The role requires excellent attention to detail and the ability to handle multiple projects simultaneously. The specialist will collaborate with researchers to ensure that their work adheres to journal and institutional standards.

- Currently pursuing or recently completed a degree in any discipline (Master’s preferred).

- Strong skills in Microsoft Office and reference formatting.

- Excellent written and verbal communication.

- Familiarity with academic publishing workflows.

- Ability to manage deadlines and coordinate across teams.

- Exposure to cutting-edge global research.

- Professional growth and training opportunities.

- Flexible work arrangements.

- Performance based Incentives.

The Research Support Specialist will provide end-to-end assistance to researchers, scholars, and clients by offering high-quality support in literature search, data organization, reference management, and formatting. The role requires excellent attention to detail and the ability to handle multiple projects simultaneously. The specialist will collaborate with researchers to ensure that their work adheres to journal and institutional standards.

- Bachelor’s degree in any discipline (Master’s preferred).

- Strong skills in Microsoft Office and reference formatting.

- Excellent written and verbal communication.

- Familiarity with academic publishing workflows.

- Ability to manage deadlines and coordinate across teams.

- Exposure to cutting-edge global research.

- Professional growth and training opportunities.

- Flexible work arrangements.

- Performance based Incentives.

The Research Support Intern will provide end-to-end assistance to researchers, scholars, and clients by offering high-quality support in literature search, data organization, reference management, and formatting. The role requires excellent attention to detail and the ability to handle multiple projects simultaneously. The specialist will collaborate with researchers to ensure that their work adheres to journal and institutional standards.

- Currently pursuing or recently completed a degree in any discipline (Master’s preferred).

- Strong skills in Microsoft Office and reference formatting.

- Excellent written and verbal communication.

- Familiarity with academic publishing workflows.

- Ability to manage deadlines and coordinate across teams.

- Exposure to cutting-edge global research.

- Professional growth and training opportunities.

- Flexible work arrangements.

- Performance based Incentives.

Job Location : Dholka, Near to Ahmedabad, Gujarat

About the Company :

Company : Cadila Pharmaceutical Ltd.

About Us : Cadila Pharmaceuticals Ltd, is one of the Largest Privately- held Pharmaceuticals companies in India. Over the past seven decades, We have been developing and manufacturing affordable medicines for the patients around the world.

Our innovation- led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

Being a care-focused, research-driven company, we are committed to complying with the highest ethical standards in the clinical research and medical practice. We lead our industry in demonstrating the application of cutting edge research to ethical business practices in producing the alchemy of optimum health outcomes for all.

About the Role :

To leverage my expertise in formulation development and regulatory compliance to develop stable and bioequivalent solid oral dosage forms for global markets, ensure successful technology transfer to manufacturing facilities, support regulatory submissions, address agency queries, and provide technical support for commercial production, contributing to the overall growth and compliance of the organization.

Responsibilities :

• To develop Stable and Bioequivalent solid oral products for US, Europe, ROW and Domestic Markets.
• Technology transfer of developed products to plant level, this includes all TTD-related works.
• To collect and compile all data and submit to respective regulatory agencies.
• To address DCGI/ regulatory agency queries as per requirement.
• To extend support to plant for any commercial trouble shooting.

Qualifications :

Ph/D

Required Skills :

• Formulation Development (solid oral dosage forms: tablets, capsules)
• Pre-formulation Studies
• Bioequivalence Study Design & Evaluation
• Technology Transfer (TTD)
• Scale-Up and Commercialization
• Analytical Data Interpretation
• Process Optimization & Troubleshooting
• Stability Studies (ICH Guidelines)
• Equipment Handling (e.g., granulators, blenders, tablet press, coating machines)
• Quality by Design (QbD)

Preferred Skills :

Hands-on Experience with Formulation and Development

Pay range and compensation package :

8 LPA to 12 LPA

Job Location : Dholka, Near to Ahmedabad, Gujarat

About the Company :

Company: Cadila Pharmaceutical Ltd.

About Us: Cadila Pharmaceuticals Ltd, is one of the Largest Privately- held Pharmaceuticals companies in India. Over the past seven decades, We have been developing and manufacturing affordable medicines for the patients around the world.

Our innovation- led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

Being a care-focused, research-driven company, we are committed to complying with the highest ethical standards in the clinical research and medical practice. We lead our industry in demonstrating the application of cutting edge research to ethical business practices in producing the alchemy of optimum health outcomes for all.

About the Role :

To leverage my expertise in formulation development and regulatory compliance to develop stable and bioequivalent solid oral dosage forms for global markets, ensure successful technology transfer to manufacturing facilities, support regulatory submissions, address agency queries, and provide technical support for commercial production, contributing to the overall growth and compliance of the organization.

Responsibilities :

• To develop Stable and Bioequivalent solid oral products for US, Europe, ROW and Domestic Markets.
• Technology transfer of developed products to plant level, this includes all TTD-related works.
• To collect and compile all data and submit to respective regulatory agencies.
• To address DCGI/ regulatory agency queries as per requirement.
• To extend support to plant for any commercial trouble shooting.

Qualifications :

Ph/D

Required Skills :

• Formulation Development (solid oral dosage forms: tablets, capsules)
• Pre-formulation Studies
• Bioequivalence Study Design & Evaluation
• Technology Transfer (TTD)
• Scale-Up and Commercialization
• Analytical Data Interpretation
• Process Optimization & Troubleshooting
• Stability Studies (ICH Guidelines)
• Equipment Handling (e.g., granulators, blenders, tablet press, coating machines)
• Quality by Design (QbD)

Preferred Skills :

Hands-on Experience with Formulation and Development

Pay range and compensation package :

8 LPA to 12 LPA

The International Potato Center (CIP) is a global,non-profit research organization that works to improve food security, nutrition, and incomes in developing countries through research and innovation in root and tuber crops—primarily potatoes and sweet potatoes .

CIP’s focus areas encompass a range of strategic priorities aimed at improving agricultural systems and livelihoods. These include crop improvement through the development of climate-resilient, high-yielding, and disease-resistant varieties of potatoes and sweet potatoes; sustainable farming by promoting environmentally friendly and resource-efficient agricultural practices; and nutrition and food systems , particularly through the use of biofortified crops. CIP also works to strengthen value chains and market access by supporting smallholder farmers in building inclusive and profitable value chains, while enhancing climate resilience by helping farming systems adapt to the impacts of climate change.

The International Potato Center (CIP) is seeking to recruit a highly motivated, field-oriented, and experienced Research Assistant to support a dynamic potato development initiative in South-West Haryana. The successful candidate will be based in Mahendragarh, Haryana and will be responsible for coordinating, implementing, and monitoring field-level agronomic activities across five districts.

This position offers an excellent opportunity to contribute to impactful agricultural research and development aimed at improving food security and livelihoods in the region.

The position requires a strong background in potato seed systems and agricultural practices. Practical expertise in pot-harvest management, pest and disease management, and potato production is essential. The candidate should also demonstrate the ability to prepare and disseminate technical reports, success stories, and promotional materials effectively.

The role includes strategic thinking and the ability to work collaboratively with farmers, government departments and internal project teams. While the role will primarily focus on agronomic duties, the selected candidate will also be expected to take on a wide range of responsibilities ensuring flexible and effective execution of activities as per project needs. Practical expertise in seed storage, pest and disease management, and potato production is essential. The candidate should also demonstrate the ability to prepare and disseminate technical reports, success stories, and promotional materials effectively.

Language: The candidate must be fluent in Hindi to conversate with farmers, with advanced written and oral communication skills in English.

Job Location : Dholka, Near to Ahmedabad, Gujarat

About the Company :

Company : Cadila Pharmaceutical Ltd.

About Us : Cadila Pharmaceuticals Ltd, is one of the Largest Privately- held Pharmaceuticals companies in India. Over the past seven decades, We have been developing and manufacturing affordable medicines for the patients around the world.

Our innovation- led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

Being a care-focused, research-driven company, we are committed to complying with the highest ethical standards in the clinical research and medical practice. We lead our industry in demonstrating the application of cutting edge research to ethical business practices in producing the alchemy of optimum health outcomes for all.

About the Role :

To leverage my expertise in formulation development and regulatory compliance to develop stable and bioequivalent solid oral dosage forms for global markets, ensure successful technology transfer to manufacturing facilities, support regulatory submissions, address agency queries, and provide technical support for commercial production, contributing to the overall growth and compliance of the organization.

Responsibilities :

• To develop Stable and Bioequivalent solid oral products for US, Europe, ROW and Domestic Markets.
• Technology transfer of developed products to plant level, this includes all TTD-related works.
• To collect and compile all data and submit to respective regulatory agencies.
• To address DCGI/ regulatory agency queries as per requirement.
• To extend support to plant for any commercial trouble shooting.

Qualifications :

Ph/D

Required Skills :

• Formulation Development (solid oral dosage forms: tablets, capsules)
• Pre-formulation Studies
• Bioequivalence Study Design & Evaluation
• Technology Transfer (TTD)
• Scale-Up and Commercialization
• Analytical Data Interpretation
• Process Optimization & Troubleshooting
• Stability Studies (ICH Guidelines)
• Equipment Handling (e.g., granulators, blenders, tablet press, coating machines)
• Quality by Design (QbD)

Preferred Skills :

Hands-on Experience with Formulation and Development

Pay range and compensation package :

8 LPA to 12 LPA