181 Literature Search Jobs

About us Royal Pharma is a trusted pharmaceutical company based in Mumbai. With over 15 years of experience, we specialize in advanced intermediate and API manufacturing. Our facility is USFDA Approved and holds WHO GMP Certification, ensuring the highest standards of quality, safety, and efficacy. We are also ISO 9001:2015, ISO 14001:2015, ISO 45001:2018 certified. Collaborating with top multinational companies, we have expanded our reach worldwide, with a focus on delivering trusted healthcare solutions that have a positive impact on individuals' lives. Position Summary : A research and development (R&D) chemist uses their knowledge of chemistry and chemical engineering to create and impro...

Basic Knoweledge of Organic chemistry, intrested in synthesis of impurities and intermediates of Drugs and pharmaceutical compounds. Conducting experiments as per requirement Writing and maintaining record books and project reports Recording and analysing data Plan and complete the allocated reactions in given time

- Literature search & compilation, generating chemistry new approaches & simplification areas. - Experimentation, Documentation of hard copy & SAP entry. - Bounding of expt. Data sheets & analytical observations, Submission of Lab documents. Required Candidate profile - 5+ years of experience as Research Scientist. - Excellent analytical & Interpersonal skills.

We are looking for a Patent Search Analyst to join our IP Search Team in Noida for fixed term. This is a great opportunity to work with Fortune 100 clients to support them on various phases in IP Life cycle management. The team member will work on various projects such as Prior-art Searching (Patentability/Validity/Invalidity), Evidence-of-Use, Freedom-to-Operate searches etc. in chem/Pharma domain. We would love to speak with you if you have skills in any of the above-mentioned services and/or have the aptitude to work on emerging technologies. About You experience, education, skills, and accomplishments Bachelors Degree or equivalent in Life Sciences, Biotechnology or related domain 5 Year...

Job Summary: We are seeking a skilled and motivated Research Scientist to join our Formulation & Development (F&D) Oral Solid Dosage (OSD) team. The ideal candidate will be responsible for the design, development, and optimization of oral solid dosage forms (tablets, capsules, etc.) from concept to commercial scale. The role involves conducting pre-formulation studies, formulation trials, process optimization, and technology transfer to manufacturing sites while ensuring compliance with regulatory and quality standards. Key Responsibilities: Design and develop robust formulations for oral solid dosage (OSD) products, including tablets, capsules, and modified-release systems. Conduct pre-form...

Responsibilities: Multiple and multistep reaction handling at time. Normality & molarity. Good hand in HPLC /GC Basic. Handling reaction of bromination, chlorination, reduction, esterification, acylation, Grignard Reaction. Synthesis. Literature search & ROS Finalization. Required Skills Synthesis Process Logical Team Player Required Qualification: - M.Sc - Organic Chemistry

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

As a Junior Executive-Tech Transfer at a leading pharmaceutical company in Hosur, Tamil Nadu, your role will involve the following responsibilities: - Involving in the batch execution activities for tech transfer & site transfer products. - Reviewing documents as per the requirements for the execution of tech transfer & site transfer products. - Applying for Test license for tech transfer & site transfer products. - Preparing & ensuring availability of item codes for raw materials, primary packaging materials, filter & tubings for tech transfer & site transfer products. - Conducting product and equipment gap assessment for the tech transfer & site transfer products. - Preparing engineering b...

Conduct NPD, process optimization, scale-up & value engineering. Develop synthetic routes, validate methods, identify raw material alternatives. Maintain documentation. Support validation & transfers. Coordinate with QA, QC & production.

Assist in lab reactions & NPD under Sr. Chemists. Support experiments, sampling, data recording & literature search. Maintain SOP compliance, perform material balance, handle lab equipment & ensure safety. Document data for scale-up.

Role Overview: You will be responsible for planning and managing medical writing for Regulatory and Pharmacovigilance Verticals in compliance with applicable regulatory guidelines. Your main duties will include providing high-quality medical and scientific writing, offering technical consultation, demonstrating subject matter expertise, managing medical writing projects, collaborating with internal and external clients, and ensuring document output compliance with client specifications. Key Responsibilities: - Provide high-quality medical and scientific writing from planning and coordination of literature search through delivery of final drafts to internal and external clients. - Offer techn...

As a Scientist III at the U.S. Pharmacopeial Convention (USP), your role involves the synthesis and delivery of USP Reference Standard candidate materials and API impurities. You will be responsible for designing and developing cost-effective synthetic routes, conducting literature searches, planning and executing synthesis of target molecules, and ensuring completion of tasks as per timelines. Your focus will be on adhering to quality management systems (QMS) and lab safety practices. Key Responsibilities: - Carry out literature searches using various scientific databases - Design synthetic routes for target molecules and prepare project proposals - Procure key raw materials and reagents ne...

As an R&D Executive at PTC - MORAIYA, your role will involve the following key responsibilities: - Preparation of Literature Search Report for various jurisdictions including USA, Australia, Brazil, China, and EMB markets - Preparation of Freedom to operate opinion for various jurisdictions including USA, Australia, Brazil, China, and EMB markets - Patent and Design Application Drafting and Prosecution - Identification of new product feasibility - Prior art searches for preparing patent invalidation ground - Trade dress and device related IP analysis - Support for litigation activities including e-discovery/paper discovery - In-house IP Portfolio Management - Preparation and review of IP rel...

About Atomgrid Atomgrid is on a mission to revolutionize the global specialty chemicals industry. We are creating a new-age, asset-light, R&D-driven brand that combines pioneering process innovation, market intelligence, and reliable contract manufacturing. We operate across sectors like Agrochemicals, Surfactants & Emulsifiers, Flavours & Fragrances, and Pharmaceuticals. Our growing team of scientists, technology engineers, and project managers is committed to delivering world-class solutions - on time, at the right price, and with unmatched quality. We are founded by IIT & IIM alumni and backed by marquee VCs in India. Read more here - https://entrackr.com/2024/05/atomgrid-raises-rs-10-cr-...

You will be joining as a Part-Time Research Assistant at Sir Ganga Ram Hospital, New Delhi, working under the supervision of Prof. (Dr.) Ashish Kumar in the Department of Gastroenterology and Hepatology. Your role will involve hands-on research tasks related to patient records and data for ongoing studies. - **Key Responsibilities:** - Daily presence in the hospital for 4 hours - Extracting data from medical records and case files - Interacting with patients for data clarification when necessary - Completing structured proformas/CRFs - Conducting literature searches on platforms like PubMed and Google Scholar - Assisting with basic statistical analysis using Excel/SPSS - Supporting in manusc...

New Chemical Entity- Design & Development (Research & Development) 1. Design & Discover NCE molecules a. Literature search and design route of synthesis b. To help in designing patentable structures of pharmacophore (prodrug design) c. IPR clearance d. Design routes of synthesis e. Synthesis of NCE’s molecules to generate library 2. Synthesis process development and validation a. Development of non-infringing rout of synthesis for lead compound b. Feasibility study c. To finalize the route of synthesis. d. Experiment design according to final route of synthesis e. Development and optimization of synthesis process f. Process Validation 3. Interpretation of analytical data (HPLC, GC, SOR, etc)...

Role To execute activities related to R&D Peptide Process Development & Scale-ups, along with a group comprising of Research Officers/ Research Assistants in co-ordination with Team/Group Leader Details Of Previous Work Experience (Mandatory Requirement) Literature search and ROS (Route of Synthesis) finalization Basic knowledge of Orthogonal protected amino acid and Peptide Solid phase peptide Synthesis/Oligonucleodtide Synthesis Handling of hazardous chemical like Trifluoroacetic acid Knowledge of handling of analytical HPLC/Oligo Synthesis Purification using Preparative HPLC Preparative column packing and usage. Computer literacy etc. Knowledge of Phosphoramidalin /handling/storage Job De...

Literature search, product understanding, data interpretation for product to be undertaken for development. Design of primary product strategy, preparation of product strategy for discussion with group leader/team leader. Planning and execution of product development work to achieve desired product profile and data compilation Execution and evaluation of various formulation optimization trials and process optimization trials and data compilation Laboratory notebook writing and assistance in documentation of controlled documents and compilation the development data Execution of scale up, exhibit batches, characterization batches, process validation batches and commercial batches at manufactur...

Literature search, product understanding, data interpretation for product to be undertaken for development. Design of primary product strategy, preparation of product strategy for discussion with group leader/team leader. Planning and execution of product development work to achieve desired product profile and data compilation Scheduling the work plan in consultation with group leader/ reporting authority for timely completion of the projects based on priority assigned. Execution and evaluation of various formulation optimization trials and process optimization trials and data compilation Laboratory notebook writing and assistance in documentation of controlled documents and compilation of t...

Job purpose Ecolab is a trusted partner at nearly three million customers locations, and it is the global leader in Water, hygiene and infection prevention solutions and services that protect people and vital resources. Around the world, customer in the food, healthcare, hospitality and industrial markets choose comprehensiveEcolabs solutions, data-driven insights and personalized service to advance food safety, maintain clean and safe environment, operate efficiently and achieve sustainability goals. To support the customers in IMEA market, Ecolab has established a state-of-the-art Research, Development and Engineering (RDE) center in Pune. We are seeking candidate who has strong collaborat...

Responsibilities: Synthetic Chemistry / Lab Work Perform multi-step organic synthesis of target molecules as per project requirements. Conduct reaction monitoring, work-up, purification, and isolation of intermediates and final products. Maintain accurate lab records and notebooks (ELN or manual) as per GLP standards. Process Development Assist in the optimization of reaction conditions to improve yield, purity, and scalability. Conduct literature searches and suggest alternative synthetic routes under supervision. Evaluate critical process parameters through small-scale experiments. Analytical Coordination Coordinate with the analytical team for sample submissions, impurity profiling, and m...

As a Product Development Scientist, your role involves conducting literature searches, gaining a comprehensive understanding of products, and interpreting data for product development. You will be responsible for designing primary product strategies and preparing them for discussion with group leaders or team leaders. Your tasks will include planning and executing product development work to achieve the desired product profile, as well as compiling data. Key Responsibilities: - Execution and evaluation of various formulation optimization trials and process optimization trials, along with data compilation. - Writing laboratory notebooks and assisting in the documentation of controlled documen...

As a PTC - CHANGODAR R&D Executive, your role will involve the formulation development of topical dosage form and oral liquid dosage form for regulatory markets. Having additional experience on solid dosage form will be advantageous. Your key responsibilities will include: - Conducting literature search for assigned projects - Planning and organizing day-to-day research activities in collaboration with the group leader to ensure timely completion of projects - Preparing various documents such as PDR, MFC, BMR, scale-up protocol, and other technology transfer and regulatory documents - Providing support in the manufacturing of clinical, scale-up, and exhibit batches as and when required Quali...

Experienced in Process development, scale-up of intermediates, APIs from lab level to manufacturing scale. Experience in working at SBP facility (strategic business partner) to execute plant batches. Delivery of assigned projects, on time with desired quality and quantity. Handling of projects from gm to multi kg scale. Good knowledge in synthetic organic chemistry and analytical data interpretation skills. Literature search and troubleshooting of chemistry issues encountered during the project execution including identification and characterisation of potential impurities. Good documentation practise, laboratory notebook writing in compliance with IPM guidelines. On time preparation of expe...

Job Title Executive API R&D Business Unit R&D1 Regulatory Affairs Job Grade G12A Location : Baroda At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, you'll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other's journeys. Role To execute activities related to R&D impurity synthesis, along with a gro...