132 Literature Search Jobs

Role and responsibility : Literature search related to formulation / API. To prepare FTO Report for formulation, API and intermediates. Ensure updation of the report. Patentability and analysis and drafting of patent application. Search on tools like SciFinder, Orbit

As a Chemical Research Scientist C in the R&D Department in Bangalore, your role involves conducting literature search and review using basic software knowledge like Sci-Finder, Chem-draw, and other databases. You will also need to have a basic understanding of AI & Chat GPT. Your responsibilities include: - Executing synthesis and scale up of small organic molecules/intermediates, active ingredient/polymers/dispersions to multi-kilogram quantities under the supervision of the department head, adapting to evolving project requirements. - Employing techniques such as column chromatography, recrystallization, fractional, column & vacuum distillation, and different techniques. - Utilizing HPLC,...

Company Name: Oneiro Lifecare Pvt Ltd (Pharma API Company) Designation: Research Assocaite Location: Ekalbara -Vadodara Immediate Joining Preferred. Role & responsibilities: Conduct research and experiments related to process development, scale-up, and optimization of APIs. Develop, optimize, and validate synthetic processes ensuring efficiency, safety, and quality. Analyze experimental data, prepare technical reports, and present findings to the team. Collaborate with cross-functional teams including Quality, Production, and Analytical departments. Maintain lab documentation and ensure compliance with Good Laboratory Practices (GLP) and safety protocols. Assist in troubleshooting process is...

Understand the project requirements & deliverables from supervisor/manager Carry out literature search by using SciFinder, Reaxys and other search engines

1.Understand the project requirements & deliverables from supervisor/manager 2.Carry out literature search by using SciFinder, Reaxys and other search engines 3.Comprehend and discuss the MSDS with supervisor/ team members.

Understand the project requirements & deliverables from supervisor/manager.Carry out literature search by using SciFinder, Reaxys and other search engines.Comprehend and discuss the MSDS with supervisor/ team members

Understand the project requirements & deliverables from supervisor/managerCarry out literature search by using SciFinder, Reaxys and other search engines.Comprehend and discuss the MSDS with supervisor/ team members.

Your Day-to-Day Tasks Include: 1. Initiating first level contact with Inbound and Outreach leads. 2. Creating and executing an outreach strategy in collaboration with the PDR Managers and PDR team leads.

1. Understand the project requirements & deliverables from supervisor/manager 2. Carry out literature search by using SciFinder, Reaxys and other search engines Required Candidate profile 3. Comprehend and discuss the MSDS with supervisor/ team members.

Responsibilities : 1. Responsible for robust and efficient implementation 2. Suggest technical solutions for short and long term

JOB DUTIES AND RESPONSIBILITIES (Please Mention In Below Table) 1. Understand the project requirements & deliverables from supervisor/manager 2. Carry out literature search by using SciFinder, Reaxys and other search engines

1.Understand the project requirements & deliverables from supervisor/manager 2.Carry out literature search by using SciFinder, Reaxys and other search engines 3.Comprehend and discuss the MSDS with supervisor/ team members.

R&D (Synthesis) -Agrochemical Industry-Saykha,Gujarat. Capital Placement Services Industry IT Software - Application Programming / Maintenance Qualification M.Sc Key Skills Green Field Projects UPLC Gujarat R&D (Synthesis) PDR R&D Develo

As a Medical Content Writer, you will be responsible for: - Reviewing promotional and medical communication materials for various client products to ensure they are medically accurate, scientifically rigorous, truthful, balanced, relevant to the product and therapy area, compliant with pharma regulations and guidelines, and supported by authentic and up-to-date references. - Developing and updating content for various medical materials, conducting literature searches to identify appropriate references, tracking and auditing assets for various purposes. - Developing and reviewing content for various deliverables, meeting quality requirements as per client satisfaction metrics, within assigned...

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization collaborating with global health and science experts to develop quality standards for medicines, dietary supplements, and food ingredients. At USP, scientific excellence is driven by fairness, integrity, and global collaboration. With over 1,300 professionals across twenty locations, USP aims to strengthen the supply of safe, high-quality medicines worldwide. USP values inclusive scientific collaboration, recognizing that diverse expertise enhances the development of trusted public health standards. The organizational culture supports equitable access to mentorship, professional development, and leadership oppo...

The ideal candidate should possess prior experience in API process development activities along with a solid understanding of API Kilo lab and pilot plant operations. Your responsibilities will include conducting process development activities such as feasibility studies, optimization, validation of assurance batches, identification of critical process parameters and quality attributes. Additionally, you will be responsible for preparing Process Development Reports, scale-up activities, and working in the kilo lab environment. Your role will involve studying and modifying reaction/process conditions in accordance with Quality by Design (QBD) principles to ensure the successful production of ...

This job is with Johnson & Johnson, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. At Johnson & Johnson,?we believe health is everything. Our strength in healthcare innovation empowers us to build a?world where complex diseases are prevented, treated, and cured,?where treatments are smarter and less invasive, and?solutions are personal.?Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.?Learn more at ht...

You will be responsible for the formulation development of Pharmaceutical and Nutraceutical products including tablets, capsules, effervescent tablets, sachets powders, and liquid formulations. This involves conducting literature search and patent search for the formulation, as well as developing cost-effective and fast production processes along with stable formulations. You will be required to create MFR and relevant specifications, facilitate tech transfer, and maintain documentation. Additionally, you will need to address any ongoing issues in the existing formulations. The ideal candidate should have 7 to 10 years of experience in this field. If you are interested in this opportunity, p...

Responsible for managing formulation development of Solid Oral dosage forms for global markets. Oversees pre-formulation, patent search, documentation, compliance, and team guidance as per regulatory standards. Required Candidate profile Pharma professional with 7–10 years in formulation development, strong regulatory knowledge, documentation, data analysis & proven team leadership skills. Share CV- stuti.naik@enaltec.com

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization collaborating with global health and science authorities to develop quality standards for medicines, dietary supplements, and food ingredients. With a core value of Passion for Quality, USP aims to strengthen the supply of safe, quality medicines and supplements worldwide through the efforts of over 1,300 professionals across twenty global locations. At USP, inclusivity is highly valued, fostering an organizational culture that offers mentorship and professional growth opportunities. Emphasizing Diversity, Equity, Inclusion, and Belonging, USP strives to build a world where quality in health and healthcare is a...

Perform Literature search/ Literature review for the products as per the required market. erform comprehensive literature search and review for assigned products across scientific, clinical, and market-related domains. Analyze, summarize, and synthesize information from peer-reviewed journals, regulatory databases, patents, and industry reports. Prepare clear, concise, and well-structured reports highlighting key findings, trends, and insights relevant to product development and market positioning. Maintain proper documentation of reviewed literature as per organizational and regulatory standards. Collaborate with cross-functional teams (R&D, Regulatory, Marketing) to provide evidence-based ...

Develop and deploy AI-based applications leveraging LLMs and Generative AI models like GPT, Gemini, or similar frameworks Build scalable backend systems using Python, ensuring seamless integration with UI/UX components Design and optimize generative AI models to address diverse business challenges Fine-tune pre-trained LLMs to align with specific use cases Work closely with cross-functional teams, including data scientists, UI/UX developers, and product managers, to deliver robust solutions Collaborate with clients to gather requirements and develop customized AI capabilities Deploy solutions on cloud platforms (Azure, AWS, or GCP) and ensure system scalability and performance

Job Description Position: Junior research scientist (JRS)/Research scientist (RS) Job Location: - Plot No. 214, Borsad - Tarapur Road, Ta: Petlad, Dist: Anand, Gujarat, India. Department: R&D / Formulation Experience: 3-6 years in Nutraceuticals Formulations. Industry: Nutraceutical / Food / Pharma Manufacturing Reports To: Manager FRD. Job Type: Full-Time Company Profile: - Pharmanza Herbal Pvt. Ltd. is one of the few companies which is focusing on standardizing and proving the efficacy of Herbal products. Our strong supplier base, fully equipped R&D facility, FDA approved manufacturing facility, infrastructure for conducting human trials as well as our formulations unit provides a one stop...

As a Formulations Scientist located in Hyderabad, India, you will be responsible for developing oral solid dosage forms of both Non-DEA and DEA substances. Your key functions will include conducting Literature Search, Pre-Formulation, and Formulation Design to ensure the development of stable, Bioequivalent, and Manufacturable generic solid oral formulations. Your responsibilities will involve being a mentor and motivator to your team. You will be tasked with developing robust formulations and processes for immediate release and modified release tablet and capsule dosage forms. Additionally, you will evaluate patents, develop non-infringement strategies, and have the capability of developing...

You will be working at Silmed Scientific, an organization dedicated to public health safety through scientific evaluation and assessment of healthcare products. The company aims to ensure the global availability of safe products and fosters a unique working culture. As a Regulatory Medical Writer at Silmed Scientific, your primary responsibilities will include: - Authoring and reviewing Regulatory submission documents for pharmaceutical marketing authorization in Europe and the United States. - Developing Common Technical Document (CTD) modules like nonclinical and clinical overviews & summaries (Module 2.4, 2.5, 2.6, and 2.7), expert reports, safety & efficacy summaries, as well as Aggregat...