183 Literature Search Jobs - Page 7

R&D (Synthesis) For Agrochemical Industry in Saykha, Bharuch, Gujarat 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 3 Comprehend and discuss the MSDS with supervisor/ team members. 4 Identify and mitigate any potential safety risk with the help of Manager 5 Plan, setup, monitor, and workup chemical reactions independently 6 Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) 7 Isolate product and Optimize reaction conditions for improved yields and output 8 P...

Role & responsibilities : Chemical Researcher & Development Udyog Vihar, Ecotech-II, Udyog Vihar, Greater Noida, Uttar Pradesh 201306, India Full-time Company Description At TAPI, were not just a companywere a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czec...

Design and implement Snowflake data models, ensuring efficient data storage, retrieval, and processing. Work closely with data engineers and analysts to build robust, scalable data solutions.

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 Plan, setup, monitor, and workup chemical reactions independently Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc.) Isolate product and Optimize reaction conditions for improved yields and output Purify compounds by different methods using chromatography, distillation and crystallization etc. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Scale up of R&D developed compounds to k...

Walk-in Drive at Baroda Date of Interview : Sunday, 29 June 2024 Time : 9.30 am 5.00 pm Department : Formulation Research & Development Solid Orals Qualification :M. Pharm Experience : 2 to 6 yrs Venue of Interview : Sun Pharmaceutical Inds. Ltd, Sun Pharma Road, Tandalja , Baroda - 390012 Brief Job Description 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 optimizati...

Role & responsibilities 1. Good knowledge of synthetic organic chemistry. 2. Performing literature searches for the molecules that reaction is being carried out and understanding of the chemistries Strong skills in designing, optimizing, and scaling up synthetic chemical processes. 3. Plan and conduct experiments for chemical synthesis, ensuring the process can be reproduced and scaled up efficiently. 4. Design scalable synthetic processes that avoid patent infringement, especially for API (Active Pharmaceutical Ingredients) development. 5. Improve processes to make them industrially feasible, reduce costs, and enhance efficiency for existing products. 6. Validate synthetic processes at both...

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...

Roles and Responsibilities Responsibilities: Scientific web research to collect information related to health and environmental hazard of substances present in the chemical products. Review of Scientific articles. Interpretation of data from literature by referring international guidance. Study report preparation with the literature findings Preparing globally compliant document for supply chain communication. SDS Authoring and updating the Safety Data Sheets (SDS) with regulatory requirements Skilled in regulatory compliance and chemical safety, Lisam exess , 1907/ 2006 regulations, product stewardship etc Desired Candidate Profile BE/ Btech/ Mtech / Msc - Biotechnology, Biochemistry, Chemi...

Role and Responsibilities Do literature search for a given step(s) / molecules and support in LSR Organize for relevant patents and papers from literature Developing, synthesizing, and analyzing peptides using various techniques like Solid & Liquid Phase Peptide Synthesis (SPPS), LC-MS, and NMR Researcher will be responsible for characterizing peptides, ensuring quality control, and contributing to research projects by designing experiments and analyzing data Developing and executing synthetic strategies for complex molecules. Purifying and analyzing synthesized peptides to assess sequence and purity. Understanding and applying principles of peptide chemistry, including the use of protecting...

Role & responsibilities : Key Responsibilities Conduct medical review of study related documents Prepare high quality medical rationale documents for agency submission Periodic Safety review Medical monitoring Develop clinical rationale for new products. Competencies and exposure to succeed in the role. Previous experience in medical review of clinical study documents (trial and BA/BE). Knowledge of clinical development for different regulatory such as USFDA, IND, EMA, JFDA. Familiarity with medical coding dictionaries (e.g., MedDRA) and safety reporting Strong attention to detail and ability to work with complex medical data. Effective communication and interpersonal skills to collaborate w...

Characterization of marketed product wrt market requirements Knowledge of ICH stability conditions and compilation of analytical data Preparation of documents like PDR, stability protocol, development report writing FDR/PDR Required Candidate profile Candidate should perform literature search Looking candidates for PDR (Formulation & Development ) Dept. Candidate should have experience in solid oral dosage (Regulated Market- USA/EU/ South Africa)

Role and Responsibilities Literature search review, segregation, compilation and ROS proposals for a given step(s) / molecules Coordinate and arranging raw materials / chemicals from different vendors / plants To review the processes for potential impurities in the beginning itself and planning for their preparation. To review RMC sheet and process operations to identify areas of cost improvement, operational ease and recovery and recycling to have most cost-effective processes To prepare and review reports such as safety, vendor qualification reports, process development, ACMI report, Nitrosamine assessment for customers Contribute novel ideas by way of participation during technical discus...

Minimum 3-4 years of relevant experience in building robust and scalable design Proficiency in UX design tools such as Figma, Sketch, Adobe XD, or InVision for creating wireframes, prototypes, and user flows. Ability to create and interpret personas, user journey maps, and task analysis to inform design decisions. Proficiency in designing intuitive, accessible, and responsive interfaces that comply with WCAG accessibility standards.

Looking candidates for PDR (Formulation & Development ) Dept. 2-7 years of relevant experience in solid oral dosage (Regulated Market) Roles and Responsibilities 1.Candidate should perform literature search 2.Pre formulation development Required Candidate profile 1.knowledge of documents – Master formula card, Bill of Material, stability protocol 2.Preparation of various documents like PDR, stability protocol, development report writing FDR/PDR

Company Name : Oneiro Lifecare Pvt Ltd (Pharma API Company) Designation: Group Leader R & D Location – Ekalbara -Vadodara Role & responsibilities : 1. Literature search, route scouting and ROS finalization. 2. Prepare the cost estimation sheet after literature, feasibility and lab validation. 3. Indent the raw materials. 4. Design experiment for feasibility and optimization. 5. Synthesis of impurity standards and reference standards for intermediates, finished product and its characterization. 6. Prepare scientific documents like SER & TTD and share to QA. 7. Transfer the technology of API/intermediates to production department and provide the support during execution. 8. Support to producti...

Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. We have opening for Formulation Research & development for OSD. Position : Executive or Sr Executive Exp 2 - 8 Yrs. Job Location: Pashamylaram - Patancheruv (Telangana State) Salary : As Per Company Norms Qualification: M .Pharm (Pharmaceutics only). Job Description : 1) Candidate must have knowledge Prototype & Product Development. 2) Must have Literature Search. 3) Scale-up Batches, Exhibit Batches, DOE Experiments. 4) PDR Preparation & Development related documentation. 5) Experience in US ,EU Markets. 6) Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S rel...

Project Role : Application Tech Support Practitioner Project Role Description : Act as the ongoing interface between the client and the system or application. Dedicated to quality, using exceptional communication skills to keep our world class systems running. Can accurately define a client issue and can interpret and design a resolution based on deep product knowledge. Must have skills : HPE Network Management Center Good to have skills : Python (Programming Language) Minimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Role:Monitoring Tool SpecialistRole Description:Act as the ongoing interface between the client and the system or applicati...

Role & responsibilities 1. Literature Search, Pharmacopoeia and Patent Search, Review and Discussion and Documentation. 2. Application of NOC, Test License, Manufacturing and Import License 3. Reference product Characterization, Manufacturing and Import License. 4. Reference product Characterization, Reverse Engineering and prototype development. 5. Preformulation study, Manufacturing of bench scale trials for formulation development. 6. Manufacturing of process optimization batches, scale up batches and submission batches. 7. Preparation of Bill of Material, Master Formula Record for manufacturing of submission batches. 8. Preparation of Product development Report for regulatory filing of p...

Job Description: 1.Candidate must have knowledge Product Development, Characterization, Literature Search, Prototype Development, Scale-up Batches, Exhibit Batches, DOE Experiments , PDR Preparation & Development related documentation. Experience in US ,EU Markets .Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D.Role & responsibilities Position : Executive/Sr Executive/Asst Manager Experience : 3 12 Yrs. Qualification: M. Pharm -Pharmaceutics Total Exp: Current CTC: Exp CTC : Notice Period: Current Designation:

Hi, Greetings from Biophore India Pharmaceuticals!! We are hiring for Synthesis R&D /Process R&D/CRO Experience: 3 to 6 Years Qualification: M. Sc ( Organic Chemistry) Walk In date : 19th November 2024, Tuesday . Timings : From 10:00 AM to 02:00 PM . Preferable Male Candidates only If any one not able to attend the interviews , share your CV to " recruitments@biophore.com "

* Literature search, interpretation of analytical results and data compilation. * Planning and designing lab experiment, raw material sourcing and finding out synthetic pathways for new product/ process development. Required Candidate profile * Executing selection of synthetic routes and developing a cost effective, commercial viable and environment friendly process technologies.

Role & responsibilities RM and PM receiving and documentation of the same. Proper arrangement of the Received COA of RM and PM. Sampling of Received RM and PM, sending the samples to ADL for analysis. Preparation of indent for trial activity and ensure the availability in defined time. Taking of daily trial batches, discussion of issue with immediate supervisor. Entry of trial batch data in lab notebook and preparation of BMR for stability batches. Maintaining the files of individual products like RM and PM COA, Trial COA and Stability Reports after updation in Excel Sheet. Ensure GMP practice in Laboratory routinely. Documentation of stability batches. Calibration of instruments in the labo...

Responsibilities: Review IP landscape reports, non-infringement& FTO analysis Devise strategies for patent non infringement and invalidations Collaborate with R & D Scientist to explore design around strategies for P-IV & NCE products Conduct IP due diligence for product selection/ new opportunity identification. Support RA for patent certification, PIL clearances and declaration Monitor, review and manage ANDA litigations Conduct patentability searches, draft and file patent applications and manage prosecutions Ensure timely and effective task delivery through strategic planning prioritisation and execution.

: Medicinal chemistry; Research and development; Literature search; Scifinder / Reaxys; Design and synthesis; combiflash/Biotage; C-C coupling etc Qualifications MSC - Organic Chemistry.

Dear Respect Applicants. Greeting from Biophore India pharmaceutical Pvt Ltd. (oral solution exp) or Inject able We have opening for Formulation R&D Department. 1) Candidate must have knowledge Prototype & Product Development. 2) Must have Literature Search. 3) Scale-up Batches, Exhibit Batches, DOE Experiments. 4) PDR Preparation & Development related documentation. 5) Experience in US ,EU Markets. 6) Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. 7) Good Communication Skills. Role & responsibilities Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current C...