681 Sds Jobs - Page 4

Company Description Panaro Tech provides affordable and reliable shared storage infrastructure solutions for high-demand data environments. Founded on principles of value-added offerings and simplicity, Panaro Tech focuses on making enterprise storage affordable for Small and Medium Businesses. The company's AWANSTOR SDS offers a lightweight, cloud-ready solution for physical and virtualized infrastructure, delivering secure multitenancy, high availability, and performance monitoring, with significant cost savings compared to traditional enterprise storage solutions. Role Description This is a full-time on-site role for an Inside Sales Specialist, located in Coimbatore. The Inside Sales Specialist will be responsible for lead generation, managing customer relationships, ensuring customer satisfaction, and providing excellent customer service. The role also involves effective communication with potential and existing clients to promote Panaro Tech’s products and solutions. Qualifications Inside Sales and Lead Generation skills Customer Satisfaction and Customer Service skills Excellent Communication skills Ability to work independently as well as in a team Experience in the technology or storage solutions sector is a plus Bachelor’s degree in Business, Marketing, or related field preferred

Job Applicant Privacy Notice APPLICATION DEVELOPER Publication Date: Jul 14, 2025 Ref. No: 533915 Location: Navi Mumbai, IN About Atos Atos is a global leader in digital transformation with c. 78,000 employees and annual revenue of c. € 10 billion. European number one in cybersecurity, cloud and high-performance computing, the Group provides tailored end-to-end solutions for all industries in 68 countries. A pioneer in decarbonization services and products, Atos is committed to a secure and decarbonized digital for its clients. Atos is a SE (Societas Europaea) and listed on Euronext Paris. The purpose of Atos is to help design the future of the information space. Its expertise and services support the development of knowledge, education and research in a multicultural approach and contribute to the development of scientific and technological excellence. Across the world, the Group enables its customers and employees, and members of societies at large to live, work and develop sustainably, in a safe and secure information space. Roles and Responsibilities Implement and configure SAP EH&S modules including Product Safety, Dangerous Goods Management, Industrial Hygiene and Safety, and Waste Management. Collaborate with business stakeholders to gather requirements and translate them into functional specifications. Ensure compliance with global and local environmental, health, and safety regulations. Develop and maintain safety data sheets (SDS), labels, and reports. Integrate SAP EH&S with other SAP modules such as MM, PP, and QM. Provide end-user training and support. Participate in system upgrades, testing, and documentation. Troubleshoot and resolve issues related to SAP EH&S functionality. Requirements He/she needs to be able to solve the issues independently and work with Solution Architect. Needs to be someone who can do analysis and design, translate into build specs Should be able to understand highly customized environments without much handholding. Should be able to work across domains Here at Atos, diversity and inclusion are embedded in our DNA. Read more about our commitment to a fair work environment for all. Atos is a recognized leader in its industry across Environment, Social and Governance (ESG) criteria. Find out more on our CSR commitment. Choose your future. Choose Atos.

Job Applicant Privacy Notice SAP ESG CONSULTANT Publication Date: Jul 14, 2025 Ref. No: 534617 Location: Chennai, IN About Atos Atos is a global leader in digital transformation with c. 78,000 employees and annual revenue of c. € 10 billion. European number one in cybersecurity, cloud and high-performance computing, the Group provides tailored end-to-end solutions for all industries in 68 countries. A pioneer in decarbonization services and products, Atos is committed to a secure and decarbonized digital for its clients. Atos is a SE (Societas Europaea) and listed on Euronext Paris. The purpose of Atos is to help design the future of the information space. Its expertise and services support the development of knowledge, education and research in a multicultural approach and contribute to the development of scientific and technological excellence. Across the world, the Group enables its customers and employees, and members of societies at large to live, work and develop sustainably, in a safe and secure information space. Responsibilities Proficient in identifying GHG scope in business value chain and mapping in SAP SFM and SAP EHSM. And ESG data sourcing from SAP and non-sap systems. Experience in developing data acquisition plan for sustainability metrics in SAP Sustainability Control Tower Helping organizations for their seamless technology transformation and user enablement in SAP EHS & Sustainability area. Implement and optimize SAP EHS & Sustainability management solutions to manage their environmental, health, and safety processes. Advising on implementing sustainability strategies and initiatives with help of SAP Solutions. Responsible to RFP response/demo preparation/POC/design/configure, test, and deploy standard and customized cloud and on-premises solutions. Technical documentation for projects and PoC builds and Develop user guides and manual to facilitate end-user adoption and system usage. Requirements Candidates who have knowledge of the Sustainability Control Tower (SCT) in SAP ESG (Environment Sustainability and Governance). SAP Product Safety & Stewardship, SAP S/4 HANA EHSM, SAP Sustainability Control Tower SAP Sustainability Footprint Management, SAP Datasphere* SAP Management of Change, SAP Audit Management Workiva ESG SUMMARY:- SAP EHS consultant with 7+ years of Experience in Product Compliance, Environment, Health, Safety Management, and Sustainability processes in SAP EHS Functional consulting. Experience with successful deployment of three E2E implementation projects, multiple upgrade, and support projects. Proficient in Requirement analysis, Business blueprint, Unit, and Integration Testing/Issue resolution, Test automation, EHS master data uploading, UAT, Authorization matrix, End user training, Cutover activities, and Post go-live support in Product Safety, ERC updates, Specification Management, SDS Authoring, Dangerous Goods Management and GLM, Incident Management, Risk Assessment, Environment Management, Management of Change, Occupational Health. What we offer: Competitive salary package. Leave Policies: 10 Days of Public Holiday (Includes 2 days optional) & 22 days of Earned Leave (EL) & 11 days for sick or caregiving leave. Office Requirement: 3 Days WFO

We are seeking Site Reliability Engineers to oversee critical cloud infrastructure for our global clients. Your role involves maintaining, enhancing, and ensuring seamless continuity across multiple production environments. Responsibilities: Your core responsibilities include: - Monitoring system availability and ensuring overall system health. - Providing proactive insights on system health and recommending optimizations to prevent future issues. - Developing software and systems to manage platform infrastructure and applications. - Enhancing reliability, quality, and time-to-market for our cloud and on-premises software solutions. - Optimizing system performance to meet evolving customer needs and drive continual innovation. - Offering primary operational support and engineering for large-scale distributed infrastructure and related applications. Requirements: This is a deeply technical role focused on enhancing and maintaining production systems. We will evaluate candidates based on the following criteria: - 5+ years of experience in supporting large-scale infrastructure and cloud systems. - Proficiency in gathering and analyzing metrics for performance tuning and issue resolution. - Collaboration with development teams to enhance services through rigorous testing and release processes. - Involvement in system design consulting, platform management, and capacity planning. - Creation of sustainable systems and services through automation. - Balancing feature development speed and reliability with defined service level objectives. Technical Requirements: - Proficiency in automation technologies, particularly Terraform or Ansible. - Strong knowledge of Linux, MySQL, and scripting languages like Bash and Python. - Experience in maintaining on-premises cloud solutions such as OpenStack, Cloud Stack, etc. - Expertise in containers and container orchestration using Kubernetes. - Familiarity with monitoring systems like Prometheus, Nagios, etc., and implementing predictive analysis. - Extensive experience in maintaining high-availability systems and ensuring business continuity. - Solid understanding of distributed systems, storage, networking, SDN, and SDS. Bonus Attributes: - Familiarity with Cloud Stack, Citrix CloudPlatform, and related roles. - Experience in data centers or ISPs in a similar capacity. - Knowledge of GPU-based systems and virtualization techniques. - Background in supporting AI/ML workloads.,

Hiring Medical Coders SDS || UP TO 10 LPA|| Hyderabad, Chennai & Bangalore Min 1 year of experience is required Certified Coders and Non Certified Coders Up to 9 LPA Notice Period : 0-30 Days Relieving letter is mandatory upto 30% hike on current CTC Interested candidates can drop Your Resume To: HR Maneesha - 9603789316 through Whatsapp maneesha.axishr@gmail.com through Mail

Job Title: JAVA Azure developer ( AWS to Azure Migration expert) Experience : 4-5 Yrs. Primary Skills: Java, Spring Boot with Kubernetes Hands-on experience with Azure AWS to Azure Cloud Migration Scope of Work: Hands-on experience in migration of JAVA applications from AWS to Azure environment Analyse source architecture, Source code and AWS service dependencies to identify code remediations scenarios. Perform code remediations/Refactoring and configuration changes required to deploy the application on Azure, including Azure service dependencies and other application dependencies remediations at source code and Infra level. 4+ years of experience in application development with either Java, Spring Boot Experience in Unit testing, application testing support and troubleshooting on Azure. Experience in application deployment scripts/pipelines, App service, VMs, APIM, AKS/Microservices/containerized apps, Kubernetes, helm charts. Hands-on experience in developing apps for AWS and Azure (Must Have) Hands-on experience with Azure services for application development (AKS, Azure Functions) and deployments. Understanding of Azure infrastructure services required for hosting applications on Azure IaaS and PaaS. Tech stack details: Apigee configuration. Spring Boot REST API / Spring Server Config Confluent Kafka AWS S3 Sync connector Azure Blob Storage Azure Functions S3 to Azure Blob Storage AWS to Azure SDK Conversion (Must Have) EKS to AKS migration (Must Have) Arora PostgreSQL Data migration (Good to have)

Role & responsibilities Were Hiring | Medical Coders & QA Specialists | Immediate Joiners Preferred Open Positions Coder Roles (Min. 2 Years Experience in Speciality Required) Surgery Coder Up to 10 LPA | Chennai, Hyderabad, Bangalore IVR (Radiology) Coder Up to 7.5 LPA | Chennai EM Coder Up to 7.5 LPA | Chennai IPDRG Coder Up to 13 LPA | Chennai, Hyderabad, Bangalore QA Roles (Min. 4 Years Experience in Speciality Required) Surgery QA Up to 70K/Month | Chennai, Bangalore ENM QA Up to 60K/Month | Chennai, Bangalore ED Facility QA – Up to 60K/Month | Chennai IPDRG QA – Up to 16 LPA | Chennai, Hyderabad Key Requirements Relevant specialty experience as listed Valid certification (CPC, CCS, CIC, COC) Willingness to work from office (Chennai base preferred) Relieving letter from previous employer is a must Work from Office | Chennai, Hyderabad, Bangalore Notice Period: 0–30 Days | Immediate Joiners Highly Preferred Relieving Letter Mandatory Interested or know someone who fits? Contact Hr prathyusha - 7702498242 ( share cv via whats app ) Preferred candidate profile

Summary Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system. Assures procedures are in place to classify and maintain records. Interprets and enforces all documentation formatting, standards, policies, and operating procedure requirements. May identify submission components, communicate documentation standards and coordinate assembly of regulatory dossiers. May analyze and evaluate data, extract pertinent information, prepare information abstracts and executive summaries of material searched. May maintain extensive knowledge of product information and continuous contacts with local, regional, and divisional customers. About the Role Key Responsibilities Structured Data Submissions (SDS): Independently perform timely SDS (e.g. xEVMPD, IDMP) via RIM system, ensuring data quality and exchange with EMA including analysis and tracking of 3rd acknowledgements. Ensure Data Quality Management and timely delivery of requests for new/changes of code lists/terms including external reference data (e.g. SPOR). Provide guidance and support to cross-functional teams related to planning, submission compilation and dispatch of worldwide compliant SDS, as well as submission filing strategy, eCTD document lifecycle management and workflows, in alignment with FHIR (Fast Healthcare Interoperability Resources). Assess SDS resources and support needs and develop/implement solutions to create efficiencies. Effectively troubleshoot technical/quality issues relating to compilation, validation and dispatch of global submission outputs. Coding of Clinical Particulars: Perform coding of the Clinical Particulars attributes in Novartis Regulatory Information Management (RIM) system: Therapeutic Indications and Co-morbidity using the MedDRA dictionary, Intended effect using a controlled vocabulary, as required to ensure compliance with xEVMPD / IDMP requirements. Review and maintain MedDRA code values used in EU registrations upon MedDRA version updates by performing gap analysis of changes, and update existing values accordingly in RIM system. Review and update coding values as needed upon queries from the European Medicines Agency (EMA), for instance receipt of 3rd acknowledgment. Interactions: Liaise with GDD colleagues regarding new regulatory requirements and related business processes, to ensure proper knowledge transfer to IT business partners for system enhancement requests. Manage interactions and collaboration with RA Country Organisations (CO), Global RA and non-RA functions on regulatory and compliance maintenance activities for Authorised and Investigational medicinal products. Optimally support QPPV and PV-related processes (incl. fees), provide support for internal /external audits /inspections. Facilitate and/or participate in meetings with internal and external stakeholders (including acquisitions, partnerships and divestiture efforts). Participate as key business contributor in Technology initiatives including, but not limited to, systems upgrades, validation, implementation activities and functionality enhancements, including external service providers. General & Training: Support user training of RA end users, as required, Coach / mentor new team members. Support PQ testing and Application verification activities, as required. Support preparation of administrative procedures and Working Instructions to support system implementations. Develop, implement, and support innovative regulatory strategies and life-cycle management of RA systems, including process productivity and efficiency improvement and propose potential solutions. Identify and investigate operational needs, problems, and opportunities, contribute to the implementation of improvements within area of responsibility. Minimum requirements BS in Life Sciences (Medicines/Pharmacy) or a relevant discipline with at least 7 years of professional work experience. Master’s degree preferred (M.Pharma or MD). 4-6 years of relevant experience in structured data submissions (e.g. xEVMPD) and use of RIM systems, including familiarity with submission publishing activities. 3-5 years in Clinical coding (e.g. MedDRA, SNOMED), Labelling, Regulatory Affairs or Regulatory submission related experience. WITH SDS experience as 1st bullet, Proficient knowledge of EMAs databases (e.g. SPOR). Knowledge and experience with eCTD, xEVMPD, IDMP, Publishing Standards and applicable related tools is desirable. Experienced in using RA systems of data (RIMS, DMS, Change Control databases), systems’ data model and vocabularies. Familiar with the drug development and registration process. Solid project management, organizational and time management skills to manage multiple ongoing projects simultaneously. Familiar with global Health Authority regulations/guidelines e.g., FDA regulations, ICH and EMA guidelines/directives. Proficiency with computer programs/systems (MS office, etc.) with demonstrated ability to learn new systems quickly. Strong analytical skills and problem-solving skills. Ability to coordinate and work effectively with cross-functional teams Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl.india@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Universal Hierarchy Node Location India Site Hyderabad (Office) Company / Legal Entity IN10 (FCRS = IN010) Novartis Healthcare Private Limited Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

We are Hiring For "Medical Coders"// up to 10 LPA // Certification is Mandatory Qualification: Any Degree Experience : Minimum 1 year relevant experience is mandatory 1. IPDRG Coder : Noida / Hyd / Chennai 2. Surgery Coder : Hyderabad / Chennai / Bangalore / Noida 3. Denials : Chennai / Hyderabad 4. Radiology : Chennai 5. ENM : Chennai / Bangalore 8. IVR Radiology : Chennai 9. Obgyn : Hyderabad 10. Enm with Surgery : Chennai Work from office / Relieving is mandatory Interested candidates can share your updated resume to HR sadhvika (9100163918) ( Via What's app ) sadhvika.axishr@gmail.com ( Via Mail ) Reference are welcome.

Summary Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system. Assures procedures are in place to classify and maintain records. Interprets and enforces all documentation formatting, standards, policies, and operating procedure requirements. May identify submission components, communicate documentation standards and coordinate assembly of regulatory dossiers. May analyze and evaluate data, extract pertinent information, prepare information abstracts and executive summaries of material searched. May maintain extensive knowledge of product information and continuous contacts with local, regional, and divisional customers. About The Role Key Responsibilities Structured Data Submissions (SDS): Independently perform timely SDS (e.g. xEVMPD, IDMP) via RIM system, ensuring data quality and exchange with EMA including analysis and tracking of 3rd acknowledgements. Ensure Data Quality Management and timely delivery of requests for new/changes of code lists/terms including external reference data (e.g. SPOR). Provide guidance and support to cross-functional teams related to planning, submission compilation and dispatch of worldwide compliant SDS, as well as submission filing strategy, eCTD document lifecycle management and workflows, in alignment with FHIR (Fast Healthcare Interoperability Resources). Assess SDS resources and support needs and develop/implement solutions to create efficiencies. Effectively troubleshoot technical/quality issues relating to compilation, validation and dispatch of global submission outputs. Coding of Clinical Particulars: Perform coding of the Clinical Particulars attributes in Novartis Regulatory Information Management (RIM) system: Therapeutic Indications and Co-morbidity using the MedDRA dictionary, Intended effect using a controlled vocabulary, as required to ensure compliance with xEVMPD / IDMP requirements. Review and maintain MedDRA code values used in EU registrations upon MedDRA version updates by performing gap analysis of changes, and update existing values accordingly in RIM system. Review and update coding values as needed upon queries from the European Medicines Agency (EMA), for instance receipt of 3rd acknowledgment. Interactions: Liaise with GDD colleagues regarding new regulatory requirements and related business processes, to ensure proper knowledge transfer to IT business partners for system enhancement requests. Manage interactions and collaboration with RA Country Organisations (CO), Global RA and non-RA functions on regulatory and compliance maintenance activities for Authorised and Investigational medicinal products. Optimally support QPPV and PV-related processes (incl. fees), provide support for internal /external audits /inspections. Facilitate and/or participate in meetings with internal and external stakeholders (including acquisitions, partnerships and divestiture efforts). Participate as key business contributor in Technology initiatives including, but not limited to, systems upgrades, validation, implementation activities and functionality enhancements, including external service providers. General & Training: Support user training of RA end users, as required, Coach / mentor new team members. Support PQ testing and Application verification activities, as required. Support preparation of administrative procedures and Working Instructions to support system implementations. Develop, implement, and support innovative regulatory strategies and life-cycle management of RA systems, including process productivity and efficiency improvement and propose potential solutions. Identify and investigate operational needs, problems, and opportunities, contribute to the implementation of improvements within area of responsibility. Minimum Requirements BS in Life Sciences (Medicines/Pharmacy) or a relevant discipline with at least 7 years of professional work experience. Master’s degree preferred (M.Pharma or MD). 4-6 years of relevant experience in structured data submissions (e.g. xEVMPD) and use of RIM systems, including familiarity with submission publishing activities. 3-5 years in Clinical coding (e.g. MedDRA, SNOMED), Labelling, Regulatory Affairs or Regulatory submission related experience. WITH SDS experience as 1st bullet, Proficient knowledge of EMAs databases (e.g. SPOR). Knowledge and experience with eCTD, xEVMPD, IDMP, Publishing Standards and applicable related tools is desirable. Experienced in using RA systems of data (RIMS, DMS, Change Control databases), systems’ data model and vocabularies. Familiar with the drug development and registration process. Solid project management, organizational and time management skills to manage multiple ongoing projects simultaneously. Familiar with global Health Authority regulations/guidelines e.g., FDA regulations, ICH and EMA guidelines/directives. Proficiency with computer programs/systems (MS office, etc.) with demonstrated ability to learn new systems quickly. Strong analytical skills and problem-solving skills. Ability to coordinate and work effectively with cross-functional teams Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment To Diversity And Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl.india@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Role & responsibilities Hiring for Medical coding & QA ( ENM || SURGERY || IVR ) || Hyderabad , Bangalore , chennai CODER LEVEL (Minimum 2 Yrs in the Specific Specialty) ENM OP / IP Chennai Up to 7.5 LPA ENM Coders Chennai, Bangalore Up to 50,000/month Surgery Coders Hyderabad, Chennai, Bangalore Up to 10 LPA IVR Radiology Coders Chennai Up to 7.5 LPA Multispecialty Denial Coders Chennai Up to 50,000/month ENM Denial Coders Chennai – Up to 10 LPA QA LEVEL (Minimum 4 Yrs in the Specific Specialty) ENM QA – Chennai, Bangalore – Up to 60,000/month Surgery QA – Chennai, Hyderabad, Bangalore – Up to 70,000/month ED Facility QA – Chennai – Up to 60,000/month Preferred candidate profile Eligibility Criteria: Experience: Minimum 1 to 5+ years (as per specialty requirement) Certification: Certified coders preferred (CPC, CCS, CIC, COC, etc.) Work Mode : Work from Office Notice Period: Immediate to 30 Days Preferred Relieving Letter: Not Mandatory Interested candidates can contact HR Sujitha at : 8297250813 Let’s connect and grow together!

We Are Hiring || ENM OP Medical coders || Bangalore and Chennai || Up to 50k || Min 1 yrs exp into ENM OP coding Package: Up to 50k Only Certified Location: - Chennain Bangalore Work from Office Notice Period :- 0 to 15 days Reliving letter is not Mandate Interested candidates can share your updated resume at 9030874428 Refer your friend's / Colleagues Axis Services Preferred candidate profile min 1yr exp into Medical coder Perks and Benefits week 5 Days

Company :- In2IT EBS Pvt Ltd. Client – Govt Client Notice - Immediate joiner or 15 to 30 Days. Location – Jagdalpur (City in Chhattisgarh) Experience : 4+ Years Employment Type : Full-time Project Type : [Implementation / Support / Rollout / Upgrade] Job Title: SAP EHS Consultant Job Description: We are looking for an experienced SAP EHS Consultant to design, implement, and support SAP EHS solutions for compliance, safety, and risk management initiatives. The ideal candidate will have a strong understanding of industry regulations, SAP EHS modules, and their integration with core ERP functions. Key Responsibilities : Gather business requirements and design SAP EHS solutions. Configure and implement SAP EHS submodules: Product Safety and Stewardship (PSS) Dangerous Goods Management Industrial Hygiene and Safety Occupational Health Incident Management Environmental Compliance Design and generate Safety Data Sheets (SDS) and labels. Manage regulatory compliance content (e.g., WWI, REACH, OSHA). Integration with MM, PP, QM, and logistics for product and material compliance. Configure EHS master data including specifications, phrases, and reports. Customize workflows and notifications for incidents and audits. Support interface with 3rd party content providers or regulatory databases. Prepare documentation (functional specs, test scripts, user manuals). Provide end-user training and post-go-live support. Required Skills : 4+ years of experience in SAP EHS. Hands-on experience in at least one full-cycle SAP EHS implementation. Strong understanding of global compliance requirements and EHS processes. Experience with WWI Report Templates , DG checks, SDS authoring, and label printing. Good knowledge of SAP EHS integration with other modules (MM, SD, PP, QM). Basic knowledge of ABAP for debugging and working with developers. Strong analytical, communication, and problem-solving skills. Preferred Qualifications : Bachelor’s Degree in Environmental Science, Chemical Engineering, or a related field. SAP EHS Certification is an added advantage. Experience working in regulated industries (Chemical, Pharma, Manufacturing). Familiarity with S/4HANA for Product Compliance and Fiori apps is a plus. Knowledge of interfaces to external regulatory services (e.g., SAP Content-as-a-Service, or third-party SDS providers). NOTE : Interested Candidates can share their resumes on prerna.kumari@in2itebs.com

Role Overview: We are looking for Site Reliability Engineers to manage mission-critical cloud infrastructure for our customers globally. This role entails performing all actions required to maintain, enhance and ensuring smooth continuity of multiple production environments. Responsibilities: Your responsibilities in this role will be centered around the following: 1. Run the production environment by monitoring availability and taking a holistic view of system health. 2. Provide predictive insights into the health of the system and suggest measures to optimize and safeguard against future abnormalities. 3. Build software and systems to manage platform infrastructure and applications. 4. Improve reliability, quality, and time-to-market of our suite of our cloud and on-prem software solutions. 5. Measure and optimize system performance, with an eye toward pushing our capabilities forward, getting ahead of customer needs, and innovating for continual improvement. 6. Provide primary operational support and engineering for multiple large-scale distributed infrastructure and related applications. Requirements: This is an in-depth technical role with complete focus on the upkeep and betterment of the production systems. This role requires proven experience and the ability to handle all the aspects of the above goals. We’ll be evaluating your candidature on the following criteria: 1. 5+ years of experience and a proven track record of maintaining and supporting large scale infrastructure and cloud systems. 2. Gather and analyze metrics from operating systems as well as applications to assist in performance tuning and fault finding 3. Partner with development teams to improve services through rigorous testing and release procedures 4. Participate in system design consulting, platform management, and capacity planning. 5. Create sustainable systems and services through automation and uplifts. 6. Balance feature development speed and reliability with well-defined service level objectives. Technical Translation of the Above: • In-depth and hands-on knowledge of automation. technologies with extensive expertise in Terraform or Ansible. • In-depth and hands-on knowledge of Linux and MySQL, programming and scripting using Bash, Python/alternate. • In-depth knowledge of maintaining any on-prem cloud solutions like OpenStack/Cloud Stack/Open Nebula/vCloud etc. • In-depth and hands-on knowledge of containers and container orchestration using Kubernetes. • In-Depth and hands on knowledge on any monitoring system (Prometheus/Nagios/Zabbix/SolarWinds/ManageEngine etc.). Experience of implementing correlation and predictive analysis into monitoring of the systems. • Hands on extensive experience of implementing, maintaining high availability systems. Ensuring backup and ensuring business continuity in a seamless manner. • Thorough conceptual knowledge of distributed systems, storage, networking, SDN, SDS. Bonus attributes that will help your application: • Knowledge of Cloud Stack/Citrix CloudPlatform and involvement as an administrator/maintainer/committer/tester/support engineer. • Data centre or ISP experience in a similar role. • Knowledge of GPU based systems, Nvidia BCM, GPU Virtualisation techniques. • Worked in supporting AI/ML workloads

Role & responsibilities Assign codes to diagnoses and procedures, using ICD (International Classification of Diseases) and CPT (Current Procedural Terminology) codes. Follow up with the provider on any documentation that is insufficient or unclear. Communicate with other clinical staff regarding documentation. Search for information in cases where the coding is complex or unusual. Receive and review patient charts and documents for accuracy. Review the previous day's batch of patient notes for evaluation and coding. Ensure that all codes are current and active. Requirements: Education Any Graduate. Must have experience in : Surgery/Cardio surgery/Neurosurgery/Gastroenterology/Urology/General Surgery. 1 to 7 Years experience in Medical Coding. Successful completion of a certification program from AHIMA or AAPC. Strong knowledge of anatomy, physiology, and medical terminology. Skilled in assigning ICD-10 & CPT codes. Solid oral and written communication skills. Able to work independently. Flexible to work from office and home as required by the business. Perks and benefits Two way transport facility available Interested candidate please share their resume at ymounica@r1rcm.com

We are hiring//Medical Coders// Min 1 + yr of exp in below mentioned specialisation's IPDRG - Hyderabad , chennai, Noida,Bangalore OBGYN - Hyderabad Surgery - Hyderabad , Chennai, Noida, Bangalore EM with Surgery - Chennai , Hyderabad Denials multi-speciality - Hyderabad , Chennai Radiology - Chennai ENM - Chennai, Bangalore Ed Profee - Bangalore Position: QA Min 4 + yr of exp in below mentioned specialisation's IPDRG QA - Hyderabad, Chennai, Bangalore Denials multi-speciality - Hyderabad ED Facility QA - Chennai ENM OP QA or ENM IP QA - Chennai, Bangalore Surgery QA - Hyderabad , Chennai , Bangalore IPDRG Trainer - Hyderabad ENM with surgery Trainer - Chennai Home health QA - Hyderabad Only Certified Coders Up to 12 LPA Notice Period : 0-30 Days Relieving letter is mandatory Interested candidates can drop Your Resume To: HR Lalitha - 8179142981 through Whatsapp lalithahr.axis@gmail.com through Mail Referrals are appreciated

Role & responsibilities We Are Hiring || ENM OP / Ed facility / Surgery - Coder , QA || Chennai Location || certification is Mandatory 1, Coder - ENM Op / Surgery - 2, QA - Surgery / Ed facility / Enm op Locations:- Chennai Exp :- CODER - Min 1+ years exp as a Enm op / Surgery coder, QA - 4+ years as a ENM Op / Surgery / ed facility Coder /As a qa 6m exp Work from office Graduation & Reliving is not Mandatory Notice period:Prefers Immediate joiners, No Need relieving Letter Interested candidates can share your updated resume to HR INDHU- 9032857196(share resume via WhatsApp) Refer your friend's / Colleagues Preferred candidate profile Exp :- CODER - Min 1+ years exp as a Enm op / Surgery coder, QA - 4+ years as a ENM Op / Surgery / ed facility Coder /As a qa 6m exp

Description Brief Job Overview This is a hands-on, non-supervisory scientific position the Global Biologics department. The incumbent is responsible for providing support for the development of USP documentary standards and reference standards for biological products such as peptides, Oligonucleotides, protein, carbohydrates, Complex Biologics, Vaccines, Antibiotics, and advanced therapies. The incumbent will provide quality and technical review of scientific documents for accuracy, clarity and compliance, manage and track reference standard stability program and organize efforts for continuous process improvements. The incumbent will also focus on supporting the reference standard suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports for confirming the continued suitability of USP Reference Standards (RS). The incumbent need to be excellent team player with good collaboration/Liaising skills to complete assigned projects in time-bound manner. How will YOU create impact here at USP? In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments. The Sr. Scientist -I (RSS-Review) has the following responsibilities: Roles and Responsibilities Performs technical and quality reviews of documents to ensure a high level of document quality and compliance before QA review Manages and tracks efforts for continuous process improvements. Develops and reviews SOP’s, Operation Manuals, and training documents. Assists in investigations of quality related issues resulting from customer complaints to include root cause analysis, corrective action identification, action planning, and implementation monitoring. Supports the day to day operation of the reference standard stability program. Works with internal stakeholders to develop new and innovative standards for analytical analysis of biological products. Communicates and maintains working relationships with cross functional USP departments regarding assigned projects Supports day to day operations of the RS Stability (CSU) program covering the USP Biologics RS catalog inventory. Reviews RS testing history and drafts test protocols for CSU studies and submits to labs based on designated testing requirements and schedules. Liaisons and Assists laboratories to ensure CSU testing is completed as per protocol and in timely manner. Reviews laboratory reports, evaluates results and compares to previous data and RS attributes to assess and conclude on RS suitability for use. Compiles, assess current and historical stability testing data and prepare stability trend reports in a time-bound manner. Support the maintenance and updation of various databases documenting laboratory data and program determinations on suitability and Stability interval updates. Filing and closure of QMS elements as per QMS system when required and supports the RS Laboratory, Supporting Quality Assurance and Reference Standard Evaluation in the investigation of unexpected stability testing results Works collaboratively with various USP departments as needed on test planning, data impact assessments and appropriate determination of next steps. Prepare, present and discuss regular work updates with Team Lead and other team members Who is USP Looking For? The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: PhD. degree in Biochemistry/Biology/Pharmacy, or a related field Minimum of 7 to 10 years, or Masters degree in Biochemistry/Biology/Pharmacy or a related field with 11 to13 years of years of commensurate industrial experience. Demonstrated experience in Techical review of analytical documents in Quality Assurance. Hands-on experience with state-of-the-art analytical techniques for the characterization of recombinant therapeutic proteins, peptides, gene therapy, vaccines and carbohydrates, such as UPLC/HPLC, LC-MS, CD, Fluorescence spectroscopy, FTIR, DSC, SEC-MALS, CE-SDS (Reducing and Non-reducing), icIEF, ELISA, SPR, ddPCR/qPCR etc. Strong ability to evaluate and compile analytical testing data, ability to write technical reports related to material characterization, references standard evaluations, and method development. Demonstrated experience in analytical method development, method qualification/validation and characterization of biological products and impurities using a variety of physicochemical techniques and biological assays. Excellent technical writing, presentation and oral communication skills are required. Must be excellent team player and able to work amicably and communicate effectively with both internal and external stakeholders. Additional Desired Preferences Knowledge of USP products and services is highly desirable. Operates collaboratively at all levels of the organization in a highly technical environment. Must be able to work in a fast-paced environment and respond to shifting priorities. Well-developed interpersonal, negotiation, conflict-resolution and listening skills. Must possess the ability to multi-task and to work effectively with a team. Takes ownership and personal responsibility to ensure work is delivered on time and is of the highest possible quality. Experience working in the compendial, pharmaceutical and/or biotechnology industry strongly preferred. Supervisory Responsibilities No Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.

About the job An exciting opportunity to join our risk-based monitoring team. Risk-based monitoring (RBM) is an adaptive approach to clinical trial monitoring that directs focus and activities to critical data and processes that have the most potential to impact patient safety and data quality. In this context, the RBM team is responsible for designing, executing, and optimizing the Sanofi RBM approach to align with regulatory requirements and Sanofi's objective to drive quality, efficiency, and speed of clinical trials. The Clinical Data Curator Specialist (CDCS) is responsible for the maintaining, organizing and improving the accessibility of clinical data to support Advance Analytics having expertise in Data Manipulation, Data extraction, Data Optimization, Data Visualization etc. Understanding of AI fundamentals with knowledge of Machine learning. This role will involve working closely with a group of core Data Scientists to ensure accuracy, completeness, and relevance of the data that will used for analysis. If you are passionate about leveraging data to drive excellence in clinical trials, this is the opportunity for you. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started? Main responsibilities: Data Inventory and Organization : Maintain a comprehensive inventory of clinical data sets to ensure clear structure and long-term usability. Implement best practices for data organization and governance. Collaborative Problem Solving : Work closely with data scientists to understand data requirement and quality standards, collaborate with digital to enhance and optimize the data pipelines and integration processes. Data Extraction and Curation : Extract, curate, and prepare clinical data sets to ensure they are fit for purpose and adhere to data governance standards. Enhance data quality for use in advanced analytics. AI/Machine Learning : Hands on experience in Machine Learning and its application in clinical trials to derive meaningful insights from data. Risk Based Quality Assurance : Implement and continuously improve a risk-based quality assurance process. Ensure proper documentation of datasets used for analysis to safeguard data integrity and ensure reliable results. Develop code/workflows and optimise existing ones : Leverage domain expertise and technical knowledge to continually enhance existing code and develop new one as per changing requirements. About you Experience : Experience in a Clinical Research environment (CRO or Pharma). In depth knowledge of clinical data programming using SAS - Base, Macros, SQL/ Python/R and experienced in handling data from multiple data sources. Soft and technical skills : Learns and adapt quickly when facing new problems. Think critically and use rigorous, objective and pragmatic methods to solve multidimensional problems with effective and timely solutions. Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy Proficiency in programming languages (either SQL, Python, Advance SAS or R). A professional certification will be a nice to have. Hands on experience in data wrangling, data extraction and manipulation from diverse input data sources using advance SQL concepts. In depth knowledge of optimizing queries and joins to efficiently process large datasets of varying degree of complexity. Familiarity with machine learning (using Python packages) and their application in clinical trial In depth understanding of clinical trial related documents and clinical knowledge, e.g., Protocol, SDS, CRF and the ability to churn both structured and unstructured data to generate meaningful output. Strong analytical skills with an attention to detail. Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams. Education : Bachelor’s degree or above, preferably in a life science or mathematics-related area (e.g., computer sciences) Languages : Strong English skills (verbal and written), ability to exchange fluently in a global environment. Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave. An international work environment, in which you can develop your talent and realize ideas and innovations within a competent team A team that driving the innovation of the monitoring activities that align with future need “We believe that a Clinical Data Curator is not only collects data for storage, but you are key to brining data to life in an AI-driven world; it's a role that embodies innovation, curiosity, and the power to transform data into actionable insights. Join us as a curator of our AI future, supported by cutting-edge technology and a collaborative team environment.”

E&M, Surgery, OBGYN, Radiology | Hyderabad, Chennai, Bangalore Role & responsibilities Openings & Salary Details: E&M (Evaluation & Management) Up to 48,000/month ENM Denial Up to 10 LPA Surgery (SDS / GI) Up to 10 LPA Radiology Coding Up to 10 LPA (Minimum 3 years of experience required) Denial Coding Multispecialty Up to 10 LPA OBGYN Coding Up to 10 LPA Preferred candidate profile Minimum 1- 6 years of hands-on coding experience in E/M, Surgery , or OB-GYN . Certification preferred: CPC, CCS, COC, or equivalent . Strong knowledge of ICD-10-CM, CPT-4, HCPCS Level II . Excellent understanding of medical terminology, anatomy, and physiology. Ability to meet deadlines and maintain accuracy in a fast-paced environment. Eligibility Criteria: Experience : Minimum 1 to 3+ years (as per specialty requirement) Certification : Certified coders preferred (CPC, CCS, CIC, COC, etc.) Work Mode : Work from Office Notice Period : Immediate to 30 Days Preferred Work Locations: Hyderabad Chennai Bangalore How to Apply: Interested candidates can share their updated resume via WhatsApp to: HR Sunitha 9603931383 Email : sunithayadav.axisservices@gmail.com

Requirement Hiring Surgery Coders , Anesthesia and E&M Coders. Preferred candidate profile 1)Should carry minimum 2+ years experience in Surgery coding, Anesthesia coding 2)Work Location : Hyderabad 3)AAPC certification is mandate 4)Immediate joiners are preferred 5)Salary is not a constraint for the right candidate Note: This requirement is not for freshers Suitable can send updated CV on whatsapp : 9912305450 Thanks Priya Recruiter Excolo SoftTech Solutions

A career in our Advisory Service Delivery Centre is the natural extension of PwC’s leading class global delivery capabilities. We provide premium, cost effective, high quality services that support process quality and delivery capability in support for client engagements. Responsibilities As a Manager you’ll work as part of a team of problem solvers with extensive consulting and industry experience, helping our clients solve their complex business issues from strategy to execution. Specific responsibilities include but are not limited to: Proactively assist in the management of several clients, while reporting to Managers and above Train and lead staff Establish effective working relationships directly with clients Contribute to the development of your own and team’s technical acumen Keep up to date with local and national business and economic issues Be actively involved in business development activities to help identify and research opportunities on new/existing clients Continue to develop internal relationships and your PwC brand Job Description: SAP – Environment, Health and Safety (EHS) Roles/Responsibilities Responsible for planning and executing SAP Implementation / Development / Support activities regard to SAP EHS Understand client requirements, provide solutions, functional specifications and configure the system accordingly. Ability to create presentation/workshop decks for Blueprint that need to be conveyed and be able to present them to the client. Ability to create Process Flows in Microsoft Visio’s for the client’s proposed business processes. Ability to create Process Definition Document / Design Document (PDD) and Business Process Procedure (BPP) for the solutions provided. Ability to configure SAP EHS process and regulatory requirements to the Client's Standards & Requirements. Integration experience of the EHS Module with other SAP modules like and with external applications Legal requirements all mandatory documents print setup and configuration. Good understanding & experience of Various SAP EH&S modules in Reporting requirements (WWI Templates, Business Objects, Adobe Forms,MSDS), Support tools like Certido, SAP Solution Manager and Service Now. Experience in Product Safety & Stewardship in classic and enhanced model is must with the list of sub modules given below SDS authoring Global Label Management, Substance Volume Tracking, Spec database, Product marketability Dangerous Goods Management. Very good hands on experience to other sub module in EHS Hazardous Substance management Incident Management Rist Management Waste Management SAP EHS Occupational Health & Safety Management of Change Environment Management Experience with 3rd party content provider integration like 3E,Sphera,Enablon,Velocity and Attrion. In addition to the above the candidate should have been involved in the following activity during the life cycle of SAP implementation: Unit Testing, Cycle Testing Integration Testing User Manual Preparation User Support activities Regularly interact with the onsite team/client Provide status updates in daily/weekly conference calls Maintain cordial relationship with onsite team/client Skills/Experience Requirements MUST HAVE: 9 to 12 years of working on the EHS module in SAP implementation projects Implementation experience should be in version ECC 6 and S/4 Hana would be a plus Should have good written and oral communication skills Must be a good team player Familiarity on the basic business processes with the following Functional Areas: Document management system Engineering change management NICE TO HAVE SAP Certification on PM Module as an advantage Used Solution Manager in the implementation Basic knowledge on ABAP / EHS related support in Basis Education: BE / B.Tech confirming to the Client's Standards & Requirements. Strong configuration hands on experience in planning and execution Integration of the SAP IBP module with other SAP modules such as SAP BPC, ECC and with external applications as well. Ability to create presentation/workshop decks for Blueprint that need to be conveyed and be able to present them to the client. Good understanding of PP Discrete / Process industry processes. Ability to create Process Flows in Microsoft Visio’s for the client’s proposed business processes. End to End process knowledge for upstream and downstream data modelling. In addition to the above the candidate should have been involved in the following during the life cycle of SAP implementation: Unit Testing, Cycle Testing Integration Testing User Manual Preparation User Support activities Exposure to different implementation methodologies Regularly interact with the onsite team/client Provide status updates in daily/weekly conference calls Maintain cordial relationship with onsite team/client Must Have At least 3-year experience working in SAP IBP area, coupled with a good understanding of different IBP scenarios. 2 years of functional domain experience or 3 to 6 years of working in SAP implementation projects Should have good written and oral communication skills. Must be a good team player Must have PP master data (Bill of Material, Resource/Work center, Routing/Master Recipe and Production Version) and Batch management experience. Must have MRP execution process experience. Must have Discrete/Process-industry execution process experience. Must have Integration knowledge PP-PPDS- IBP. Familiarity on the basic business processes with the following Functional Areas: SAP PP or SAP APO PPDS SAP APO DP and SAP APO SNP NICE TO HAVE SAP Certification on APO and PP. Used Solution Manager in the implementation Worked on integration with other ECC modules Team Leading Experience would be added advantage Exposure to interfaces like ALE/IDOC or EDI/IDOC with little technical knowledge Professional and Educational Background B Tech, M. Tech, MBA, M.com, B.E, B.A, B.com Additional Information Line of Service: Advisory

You should have at least 5+ years of work experience in building infrastructure solutions based on customer requirements. The location for this position is in Chennai/Hyderabad. It is essential to have good working experience with Data Center products like X86 Servers, Storage, HCI AI Solutions. Your responsibilities will include building x86 based solutions using 3-Tier or HCI based architecture, as well as building Storage solutions such as SAN, NAS, SDS. A good understanding of server and storage virtualization options is necessary, along with knowledge of different types of workloads like Database, SAP HANA, and Big Data. You should also have a fair understanding of Cloud technology, including its suitability for workloads, building a cloud stack, and integration with public cloud offerings like Azure, AWS, and GCP. Demonstrating a consultative approach in engaging with customers to explore and understand their current landscape, suggesting modernization options, and improving efficiency will be a key part of your role. Good presentation and whiteboarding skills are required to explain solutions to customers and determine the optimal fit for their needs. Experience in working on RFPs, both in building RFPs and responding to them, would be beneficial. You will be responsible for building configurations using Lenovo tools for the infrastructure solutions proposed to customers. Supporting Business Partners by engaging with their end customers and making product portfolio and concept presentations at Marketing events or to educate partners will also be part of your responsibilities. Collaboration is key, as you should be a team player working with other Solution consultants and the Sales team towards the common goal of providing the best solution to customers and winning their confidence. This position requires a candidate who is a graduate and possesses strong teamwork and communication skills. If you are excited about being part of Lenovo's transformative journey and contributing to a more inclusive, trustworthy, and smarter future, visit www.lenovo.com for more information and updates.,

About Atos Atos is a global leader in digital transformation with c. 78,000 employees and annual revenue of c. 10 billion. European number one in cybersecurity, cloud and high-performance computing, the Group provides tailored end-to-end solutions for all industries in 68 countries. A pioneer in decarbonization services and products, Atos is committed to a secure and decarbonized digital for its clients. Atos is a SE (Societas Europaea) and listed on Euronext Paris. The purpose of Atos is to help design the future of the information space. Its expertise and services support the development of knowledge, education and research in a multicultural approach and contribute to the development of scientific and technological excellence. Across the world, the Group enables its customers and employees, and members of societies at large to live, work and develop sustainably, in a safe and secure information space. Responsibilities Proficient in identifying GHG scope in business value chain and mapping in SAP SFM and SAP EHSM. And ESG data sourcing from SAP and non-sap systems. Experience in developing data acquisition plan for sustainability metrics in SAP Sustainability Control Tower Helping organizations for their seamless technology transformation and user enablement in SAP EHS & Sustainability area. Implement and optimize SAP EHS & Sustainability management solutions to manage their environmental, health, and safety processes. Advising on implementing sustainability strategies and initiatives with help of SAP Solutions. Responsible to RFP response/demo preparation / POC / design / configure , test, and deploy standard and customized cloud and on-premises solutions. Technical documentation for projects and PoC builds and Develop user guides and manual to facilitate end-user adoption and system usage. Requirements Candidates who have knowledge of the Sustainability Control Tower (SCT) in SAP ESG (Environment Sustainability and Governance). SAP Product Safety & Stewardship, SAP S/4 HANA EHSM, SAP Sustainability Control Tower SAP Sustainability Footprint Management, SAP Datasphere* SAP Management of Change, SAP Audit Management Workiva ESG SUMMARY:- SAP EHS consultant with 7+ years of Experience in Product Compliance, Environment, Health, Safety Management, and Sustainability processes in SAP EHS Functional consulting. Experience with successful deployment of three E2E implementation projects, multiple upgrade, and support projects. Proficient in Requirement analysis, Business blueprint, Unit, and Integration Testing/Issue resolution, Test automation, EHS master data uploading, UAT, Authorization matrix, End user training, Cutover activities, and Post go-live support in Product Safety, ERC updates, Specification Management, SDS Authoring, Dangerous Goods Management and GLM, Incident Management, Risk Assessment, Environment Management, Management of Change, Occupational Health. What we offer: Competitive salary package. Leave Policies: 10 Days of Public Holiday (Includes 2 days optional) & 22 days of Earned Leave (EL) & 11 days for sick or caregiving leave. Office Requirement: 3 Days WFO

Design & Development of commercial vehicles -Goods and Passenger >3.5T to 55T Domain expert in Vehicle Architecture finalization & Vehicle Integration. Should have good assessment skills of vehicle performance parameters and be able to evaluate suitability/selection to vehicle & its application. Good Working Knowledge of all Vehicle Aggregates to deliver the best Vehicle Integration Hands on experience in complete Product Development Life Cycle right from concept to SOP, (CAD data proposal, EBOM CADBOM assessment etc.) Hands on with field issues resolutions Good knowledge of regulatory requirements of Commercial Vehicles Good knowledge of alternate fuel system and able to drive design and developments. Ex Diesel, CNG, Hydrogen fuel cell, LNG etc. Good working experience of design & quality tools; DFMEA, DVP, SOR, SDS, R/1000, GD&T Good knowledge of Manufacturing processes at Component and Vehicle levels Technical know-how of validation requirements at vehicle level. Interact with CFT for DFM, DFA, DFS clearances Ideation and implementation of IMCR activities DFMEA, DVP, problem solving techniques, NVH, VA/VE Techniques Experience in defining wiring and tubing layout through Virtual and physical auditing Experience on Vehicle Level Modularity across all platforms Shall have exposure about upcoming technologies and trends in commercial vehicles and buses. Shall lead, review and assist all Vehicle Integration assigned activities across all Platforms LCV, ICV, HCV and Buses Responsible for TCP of Products across all platforms Alignment with Platforms, COEs & all other stakeholders Result orientation with execution excellence Multiple proposal preparation with pros/cons matrix presentation First time right approach Good communication skills to interact with CFT Should have skill set of Collaboration, Agility and Boldness Have an ability to make quick decisions with anticipated risks and mitigation plans during product life cycle. Should have worked in CFT environment and ensure flawless project delivery. Should be able to participate and add value in aggregate strategy discussions Proactive approach towards work activities for project completion Proper documentation, project tracking & timely deliveries Requirements: Knowledge of design of different types of suspensions like multi leaf, Parabolic, Air suspension etc. Good knowledge on part and system level calculations Failure analysis and problem solving skills Sheet metal, castings & forgings design, brake tubes and piping layout & manufacturing process knowledge. CAD knowledge (Catia & Team center PLM) GD&T Know-how of Ride and handling, Vehicle dynamics ABOUT US SOLUTION PLATFORM DOMAIN EXPERTISE RESOURCES CAREERS