37 Literature Search Jobs

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 discussion & motivating the team members To meet EHS and compliance expectation and guiding other members Preparation and sharing presentations for various reviews with internal and external customers. Management of Laboratory and equipment, Ensuring Maintenance of inventory with the support of other team members The candidate will participate and/or lead project teams associated with process development and characterization for peptides and other modalities. Develop and characterize peptide (or other modalities) processes in the laboratory and translate them to scalable processes. Proactively advise and share knowledge and expert opinions with subordinates, peers, and senior management. Mentor staff in troubleshooting strategic and experimental issues. The position involves multi-disciplinary interactions with organic chemists, analytical chemists, engineers, IP, Regulatory and program management. The candidate will identify and nurture ideas for continuous improvement activities and initiatives within the department. The candidate will be responsible for setting project strategies, defining project responsibilities and timelines, developing control strategies, providing leadership in a matrixed team setting and developing robust processes for cGMP manufacturing. Competencies required Sound knowledge of organic chemistry, Spectroscopy, Drug Regulatory Affairs & Quality Assurance ICH Guidelines and IP understanding Good experimental hand & Scale-up knowledge Innovative thinking & excellent observance Problem Solving Ability Excellent teamwork and collaboration within & with other functions Effective communication & Presentation skills Planning & Organization Interested candidate can share their profile on jasleen.kaur@tapi.com or else share on 8076954558

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 discussion & motivating the team members To meet EHS and compliance expectation and guiding other members Preparation and sharing presentations for various reviews with internal and external customers. Management of Laboratory and equipment, Ensuring Maintenance of inventory with the support of other team members The candidate will participate and/or lead project teams associated with process development and characterization for peptides and other modalities. Develop and characterize peptide (or other modalities) processes in the laboratory and translate them to scalable processes. Proactively advise and share knowledge and expert opinions with subordinates, peers, and senior management. Mentor staff in troubleshooting strategic and experimental issues. The position involves multi-disciplinary interactions with organic chemists, analytical chemists, engineers, IP, Regulatory and program management. The candidate will identify and nurture ideas for continuous improvement activities and initiatives within the department. The candidate will be responsible for setting project strategies, defining project responsibilities and timelines, developing control strategies, providing leadership in a matrixed team setting and developing robust processes for cGMP manufacturing. Competencies required Sound knowledge of organic chemistry, Spectroscopy, Drug Regulatory Affairs & Quality Assurance ICH Guidelines and IP understanding Good experimental hand & Scale-up knowledge Innovative thinking & excellent observance Problem Solving Ability Excellent teamwork and collaboration within & with other functions Effective communication & Presentation skills Planning & Organization Interested candidate can share their profile on jasleen.kaur@tapi.com or else share on 8076954558

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.

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 production team for trouble shooting. 9. Identify cost improvement area in existing product. 10. Check lab note book and provide guidance if any. 11. Support to cross function team to resolve customer query. 12. Motivates, develop and train research staff to achieve goals. 13. To support in failure of investigation for OOS, OOT, Deviation and other failure. 14. To review and approval of standard operating procedure. 15. To review impact assessment to change control. 16. To support for new alternate vendor for key starting materials. 17. To support the manufacturing department if any troubleshooting occurs. 18. Responsible for other activities as instructed by Head R&D/ COO Technical whenever required. if interested and ready to relocate, contact on this email ID: corporate.hr@exemedpharma.com

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 related to formulation R&D. 7) Good Communication Skills. Ref to Friends or colleagues. Please share me update resume: careers@biophore.com Total Exp : Current CTC: Exp CTC: Notice Period: Current Designation:

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 application. Dedicated to quality, using exceptional communication skills to keep our world class systems running.Must Have Skills:Candidates should have 14+ years industry experience in managing tools MF NNM Applications and Excellent network analysis fundamentals and robust troubleshooting skills Good To Have Skills:MF NPS/NA/UCMDB/Sitescope/OBM and Server Operating System (Windows/Unix/Linux), Network & Application Monitoring tools Knowledge. Industry Standard tool certifications will be preferred.Job Requirements:Key Responsibilities :a. NNM/NPS/NA/iSPI's Installation/Upgrade with ApplicationFailover and HA Environment.b. NNM Integration with multiple MF Tools as well as 3rd party tools.c. NNM/NA discovery and DDP Installationd. Configuring LDAP, SMTP and SSL on NNM/NA.e. Performing Router, Switches, Firewall, Load balancer discovery/trubleshooting.f. Troubleshooting of discovery failure and inetgation related issues.g. NPS Standard and customization reports and schudling.h. Experince on NNM/NPS/NA/iSPI migration.Technical Experience:a. Installation of Installation.b. Integration with NPS/NA/UCMDB, OBM and 3rd party tools like mywizard.c. Basic and Advanced Discovery Knowledge.d. NNM/NPS/NA console, custompoll, SNMP Traps, monitoring setting.e. Scripting - Perl, Shell, etc. for any cutomization and automation in NNM. Professional Experience: Good understanding of ITIL framework Flexible to work in 24x7 environment Should have knowledge of SLAs OLAs and KPIs Well versed corporate ethics and compliance Team player who also works well independently self-motivated Work on the service improvement programs. Educational Qualification:Bachelor degree or Engineering and 15 years of full time education. Additional Information:Good communication, presentation, technical documentation, and collaboration skills. Qualifications 15 years full time education

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 products. 9. Should have knowledge on product development requirements for Regulated market (EU/UK/Canada). 10. Should have knowledge on QbD and DOE, formulation development and Process development of drug products. 11. Coordination with CFTs like: DQA, Clinicals, Regulatory, Technology transfer and production for smooth development and transfer of product from laboratory to Production floor. 12. Knowledge on IR/MR solid oral drug products. Preferred candidate profile Male candidate only

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 laboratory. Literature search and review for the newly identified products for EU/UK/Raw market. SOP preparation and submission to DQA. Ensure utility in good condition in laboratory during all development batches. Adhere Good Manufacturing Practice and Good Laboratory Practice throughout lifecycle of the product. Preferred candidate profile Should have exposure to Formulation & Development of Injectable products knowledge for regulatory market preferable along with regulatory documents preparation like PDR, MFR etc. If having basic knowledge of injectable products is added advantage.

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 CTC: Exp CTC: Notice Period: Current Designation:

Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find a culture guided by inclusion, talented peers, comprehensive benefits and career development opportunities. Come make an impact on the communities we serve as you help us advance health optimization on a global scale. Join us to start Caring. Connecting. Growing together. Primary Responsibilities Be able to interact with business users, IT and customers to define application requirements Be able to write the code and review the code of the engineers and lead engineering teams Involve in critical and complex technical discussions Be able to prioritize and manage work to critical project timelines in a fast-paced environment Comply with the terms and conditions of the employment contract, company policies and procedures, and any and all directives (such as, but not limited to, transfer and/or re-assignment to different work locations, change in teams and/or work shifts, policies in regards to flexibility of work benefits and/or work environment, alternative work arrangements, and other decisions that may arise due to the changing business environment). The Company may adopt, vary or rescind these policies and directives in its absolute discretion and without any limitation (implied or otherwise) on its ability to do so Required Qualifications Graduate degree or equivalent experience 15+ years of formal education 13+ years of hands-on experience Java/J2EE, Spring 10+ years of hands-on experience on relational and non-relational database 8+ years of experience in Agile/Devops 7+ years of hands-on experience on Micro-Service, Spring-Boot, Spring Batch 7+ years of hands-on experience of building robust infrastructure using Docker, Kubernetes 4+ years of hands-on experience on Azure COSMOS DB 4+ years of hands-on experience on Azure cloud, Kafka Proven excellent object-oriented programming skills and accomplished performance with Java technologies Proven solid ability to work collaboratively across diverse groups of business and technical stakeholders Proven solid architectural and design mindset Proven exceptional ability to communicate with both technical and non-technical people Proven detail-oriented and ability to document low to highly complex functional designs and data structures, to support business and operational requirement

Review of promotional and medical communication materials (for various client products) and ensure the content in these materials is medically accurate, scientifically rigorous, truthful and balanced, relevant to product and therapy area, compliant to various pharma regulations and guidelines and is supported by authentic and up to date references. Develop and update content for various medical materials, perform literature search to identify appropriate references to support creation/update of scientific content, track and audit assets for various purposes. Develop and review content for various deliverables meeting quality requirements as per client satisfaction metrics, within assigned timelines and with guidance from the manager. The tasks will be carried out as per assigned processes, guidelines, and SOPs with help of tools and platforms specified by the client and the manager. Responsible to follow the best practices in the department regarding - processes, communication (internal & external), project management, documentation, and technical requirements like - language, grammar, stylization, content search, summarizing, data conflicts and referencing. Participate in assigned training programs and work on assignments as per requirement. Participate in client calls as per project requirements. Compliance to quality, confidentiality and security; Adhere and follow quality systems, processes and policies; Comply to training and specifications Key Requirements: EXPERIENCE: Minimum 2 to 5 years of experience EDUCATION: MD/MDS/PhD with Post Doc (or experience)/MBBS with experience . Location: Hyderabad, Banglore, Mumbai, Delhi/Ncr, Pune Interested Candidate Please Apply - India.hr@infinitysts.com

Role & responsibilities Preferred candidate profile Lead the team

Minimum 4-5 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.

Title: Group Leader - Personal Care Level: AGM Qualification: M.Sc in Organic Chemistry, Ph.D. is desirable. Experience: In Fine Chemical / Surfactants Industry for use in Cosmetics / Personal Care products as Raw Materials / Ingredients 15 years minimum to 22 years. 4-5 Team members will report to this role. Working : Alternate Saturday off. Industry: Fine Chemicals / Surfactants Chemicals Mfg for Cosmetics / Personal Care Key Responsibilities include: Assessment of the given Molecule w.r.t. Literature Search , Route Proposition, Cost of Raw Material Contribution Calculation (RMC) Synthesis, execution planning & scheduling of Chemicals as your assigned project. Planning & execution of activities like Vendor Qualification, Generation of specifications for RMs & KRMs Liaising with Procurement to achieve milestones for lab development activity Ensure availability of all required resources for your Projects Lead & troubleshoot the validation of the developed processes in pilot & commercial plant scale.

Role & responsibilities Literature search using various search engines. Analytical Method Development of raw materials, active substances and Finished product. Analysis of raw materials, active substances and finished products. Preparation of test protocol. Experience in handling instruments like spectrophotometer, HPLC, and GC. Knowledge of analytical method validation. Knowledge of natural chemistry background and its analysis.

Role & responsibilities Ability to conduct experiments and allied activities: Must have hands on experience in all aspects of project initiation Literature search Propose possible Route of Synthesis (RoS) Understand reaction mechanism Ability to conduct experiments and monitor reactions with the aid of minimum supervision Conducting lab validation experiments, compiling data & preparation of batch/development report Adherence to online documentation, quality standards, safety standards & delivery timelines Ability to suggest ways of process optimization and come up with what-if studies Must have hands on experience in handling impurity profiling & in-process controls Conduct consistency experiments, Lab validation experiments & development report preparation Provide necessary support to kilo lab/manufacturing team Meeting project timelines, RMC & quality parameters Online maintenance of GLP & documentation as appropriate Ensuring full adherence to safety & quality SOPs Ensure safety at work through enforcement of good laboratory practices: Follow safety & quality systems in the labs Maintenance and usage of equipment/apparatus/instruments as per SOPs and general housekeeping norms Guide team members/juniors on safety protocols and ensure compliance Maintain records, data integrity and IP confidentiality: Document the reactions executed, research findings/observations accurately in lab notebooks to ensure data integrity Maintain strict IP Confidentiality and adhere to all policies To prepare the final reports as required Ensure skill development of self: Improve knowledge of organic chemistry/Analytical techniques through one-on-one discussions with supervisor/ regular classroom trainings/ project trainings/ further educational programs etc. Preferred candidate profile Qualification: M.Sc. (Organic Chemistry) Experience: 2 - 6 Years of experience in Process R&D

Role & responsibilities Process Development: Conduct research and design experiments to develop and optimize synthetic routes for API molecules. Perform literature searches for identified API molecules to determine synthesis routes, polymorphs, and analytical methods. Conduct experimental trials to assess feasibility and optimize designed synthetic routes for API molecules. Documentation: Record all experiments in the laboratory notebook (LNB) and maintain corresponding analytical data in organized folders. Design synthetic routes for the synthesis and isolation of impurities and reference standards. Ensure all documentation meets Good Manufacturing Practices (GMP) and regulatory standards. Safety and Compliance: Adhere to all safety protocols and ensure a safe working environment in the laboratory. Develop non-infringing synthetic processes based on literature, raw material availability, and polymorph studies. Stay up-to-date with industry trends, regulatory guidelines, and advancements in chemical synthesis and analytical techniques.Team Collaboration: Plan daily activities for team members, focusing on feasibility studies, process optimization, and laboratory validation. Work closely with the Analytical Research and Development (ARD) team on method development, in-process testing, and reference standards qualification. Qualifications: Education: MSc/BSc in Organic Chemistry, Experience: Minimum of 3-5 years of experience in process development and optimization in the pharmaceutical or bulk drug industry. Skills: Strong knowledge of synthetic organic chemistry and process chemistry. Proficiency in using and interpreting data from analytical instruments. Excellent problem-solving skills and attention to detail. EZective communication and teamwork skills. Ability to work independently and manage multiple projects simultaneously. Preferred candidate profile We are looking for a talented and driven R&D Chemist to join our team. The successful candidate will be responsible for developing and optimizing chemical processes for synthesizing active pharmaceutical ingredients (APIs). This role requires a strong background in synthetic organic chemistry, process development, and scale-up techniques. The R&D Chemist will collaborate with cross-functional teams to ensure the smooth transition of processes from the lab to full-scale production. Perks and benefits

Strategic Efficient contribution to the overall success of R&D by driving innovation and team performance according to objectives and targets being set by HoF of Process Innovation. Fulfilling requirements as set by Group Leader and Team Leader within specific Research Projects. Ensuring the security of intellectual property for R&D (patent applications). Operational Keep self updated on new developments and techniques in synthetic chemistry and process research Continuous documentation and reporting of all research results obtained within the area of responsibility as defined in the SOP / guideline Carrying out experiments with knowledge of SDS of starting materials and reagents used. Seek functional support actively from Senior RS/Team Leader Carrying out literature search by use of available tools (Reaxys/SciFinder/Patents etc.) Carrying out synthetic experiments safely, efficiently, capturing all the experimental procedures and data Updating the GL/TL on the functional progress/issues of the project on a regular basis Constructive and active participation in all technical and functional meetings of the Team Responsible for individual safety and housekeeping of the lab People Actively imbibing the values and philosophy of PI Industries Support Team members by providing peer feedback Foster an environment of knowledge sharing within the Team Qualification & Eligibility : M Sc / PhD in Chemistry / Organic Chemistry or M. Pharma in Pharmaceutical Chemistry Experience : PhD with 1 to 5 years & M Sc with 1 to 12 years in chemical process development / process optimization in Agrochemicals/Pharma Industry

Role & responsibilities Process Development: Conduct research and design experiments to develop and optimize synthetic routes for API molecules. Perform literature searches for identified API molecules to determine synthesis routes, polymorphs, and analytical methods. Conduct experimental trials to assess feasibility and optimize designed synthetic routes for API molecules. Documentation: Record all experiments in the laboratory notebook (LNB) and maintain corresponding analytical data in organized folders. Design synthetic routes for the synthesis and isolation of impurities and reference standards. Ensure all documentation meets Good Manufacturing Practices (GMP) and regulatory standards. Safety and Compliance: Adhere to all safety protocols and ensure a safe working environment in the laboratory. Develop non-infringing synthetic processes based on literature, raw material availability, and polymorph studies. Stay up-to-date with industry trends, regulatory guidelines, and advancements in chemical synthesis and analytical techniques.Team Collaboration: Plan daily activities for team members, focusing on feasibility studies, process optimization, and laboratory validation. Work closely with the Analytical Research and Development (ARD) team on method development, in-process testing, and reference standards qualification. Qualifications: Education: MSc/BSc in Organic Chemistry, Experience: Fresher or 1-2 years experience in process development and optimization in the pharmaceutical or bulk drug industry. Skills: Strong knowledge of synthetic organic chemistry and process chemistry. Proficiency in using and interpreting data from analytical instruments. Excellent problem-solving skills and attention to detail. Effective communication and teamwork skills. Ability to work independently and manage multiple projects simultaneously. Preferred candidate profile We are looking for a talented and driven junior R&D Associate to join our team. The successful candidate will be responsible for developing and optimizing chemical processes for synthesizing active pharmaceutical ingredients (APIs). This role requires a strong background in synthetic organic chemistry, process development, and scale-up techniques. The R&D Chemist will collaborate with cross-functional teams to ensure the smooth transition of processes from the lab to full-scale production. Perks and benefits

Reporting to (Title) Group Leader Chemistry Level E1 E4 Position Purpose The role holder shall report to the Group Leader and shall perform research activities as designing and conducting scientific experiments, analyzing and interpreting results leading to the discovery, and pre-development of innovative molecules for crop protection / crop growth with the aim of adding significant value to the business of PI. Strategic Responsibilities Actively imbibing the values and philosophy of PI Industries Efficient contribution to the overall success of CreAgro Chemistry by driving innovation and team performance according to objectives and targets being set by the Director and Head of Chemistry. Fullfilling requirements as set by Group Leader and Team Leader, e. g. within specific Research Projects Ensuring the security of intellectual property for CreAgro (patent applications, ensuring freedom-to-operate) Updating self with respect to chemistry knowledge through literature scanning to foster innovation Support the Team Leader with special focus on target setting and constantly seek functional feedback Operational Responsibilities Work with the Team to achieve and exceed targets within the frame given by the Group Leader and Team Leader Continuous documentation and reporting of all research results obtained within the area of responsibility Carrying out literature search by use of available tools (Reaxis/Scifinder/Patents etc.) Carrying out synthetic experiments safely, efficiently, capturing all the experimental procedures and data effectively Update on the functional progress/issues of the project on a regular basis and actively seek functional support from Team Leader Constructive and active participation in all technical and functional meetings of the Team Responsible for individual safety Financial Responsibilities People Responsibilities Foster an environment of knowledge sharing within the Team Maintain healthy working relationships with the related teams and departments in CreAgro Education Qualification MSc/PhD in Organic/Analytical Chemistry from a reputed University / Institute from India or overseas with excellent academic credentials Post-doctoral research experience in a reputed university is preferred Work Experience Good experimentalist with experience in industry for 1-7 years Experience of working in discovery / process / development chemistry Industry to be Hired from Agrochemical, Fine Chemical, Pharmaceutical Functional Competencies Scientific Knowledge_O Research Approach Data Analysis Experimentation Skills Interaction Complexity and Team Work Internal: Other Chemistry/Analytical Chemistry Team members Biology SCM Team Other support functions External: Chemical Logistics Service Engineers