17 Electronic Submissions Jobs in Gurgaon

Role Overview: As a Medical Biller at Gentell, you will play a crucial role in ensuring accurate and timely submission of claims to insurance companies. Your expertise in medical billing and claims submission will directly impact the efficiency and compliance of our operations. Key Responsibilities: - Prepare and submit claims to insurance companies electronically or via paper. - Review claims for accuracy, completeness, and compliance with coding standards. - Monitor rejected claims and promptly correct and resubmit them. - Collaborate with coding and collections teams to resolve any issues efficiently. Qualifications Required: - 3 years of experience in medical billing and claims submission. - Knowledge of CPT, ICD-10, and HCPCS coding standards. - Familiarity with clearinghouses and electronic claim submission processes, Brightree preferred. - Strong attention to detail and problem-solving skills.,

Job Description: AR Caller (Physician Billing / Hospital Billing)Experience: 1 to 5 yearsLocation: NoidaWork Mode: Work from Office (WFO)Interview Mode: Virtual Shift : Day and Night shift both are available Salary package : up to 5 LPA Job Responsibilities: Review and follow up on outstanding insurance claims for physician/hospital billing.Contact insurance companies via phone/email to check claim status and resolve denials or rejections.Identify issues causing payment delays and work towards claim resolution.Appeal underpaid or denied claims, ensuring maximum reimbursement.Analyze and interpret Explanation of Benefits (EOBs) and Electronic Remittance Advice (ERAs).Document all call interactions and claim follow-up details accurately.Work closely with the billing team to ensure accurate claim submission.Meet daily and monthly productivity targets.Stay updated on US healthcare policies, insurance guidelines, and compliance requirements.  Required Skills & Qualifications: 1 to 5 years of experience in AR calling for US healthcare (Physician or Hospital Billing).Strong knowledge of medical billing terminologies, insurance claim processing, and denial management.Excellent communication skills in English (both verbal and written).Familiarity with HIPAA regulations and healthcare compliance.Ability to work in a fast-paced environment and meet deadlines.Proficiency in Microsoft Office and billing software is a plus.

As a Railway Project Engineer, you will actively participate in railway projects by utilizing your expertise in project management, engineering design, and independent review. Your role will involve undertaking various railway projects and offering consultancy services in risk management, system assurance, asset management, safety audits, and more. You will be required to prepare detailed reports, tender documents, budget plans, programs, and other essential deliverables. Additionally, reviewing design documents and technical submissions will be a crucial aspect of your responsibilities. Key Responsibilities: - Prepare detailed reports, tender documents, budget plans, programs, and other essential deliverables - Offer consultancy services in risk management, system assurance, asset management, safety audits, and more - Review design documents and technical submissions - Play a key role in preparing System Assurance reports covering critical aspects like Deterministic Safety Assessment, SIL Compliance Demonstration, SCIs, RAM Analysis, FMECA, among others Qualifications Required: - Bachelor's degree in Electrical or Electronics Engineering, Systems Engineering, Computer Engineering/Science, or related fields - Minimum of 5 years of relevant experience - Previous experience working with consulting firms would be advantageous Moreover, we are seeking a self-motivated individual with excellent interpersonal skills. Strong communication, analytical, and problem-solving abilities are essential for this role. Proficiency in both written and spoken English is crucial to effectively fulfill the responsibilities of this position.,

As a Drug Regulatory Affairs Specialist at Medyur Pharmaceuticals Limited, you will be responsible for ensuring compliance with regulatory requirements for our products and driving successful product launches. You will collaborate with cross-functional teams to maintain regulatory compliance and facilitate smooth communication with regulatory bodies. Key Responsibilities: - Prepare and submit regulatory documentation such as dossiers for pre-market submissions to obtain necessary approvals. - Stay up to date on current regulatory requirements, guidelines, and industry trends in global markets. - Develop and maintain strong relationships with regulatory bodies to support approvals. - Review changes to regulatory policies and recommend actions for continued compliance. - Conduct regulatory impact assessments to evaluate potential changes affecting product development. - Maintain regulatory files, records, and reports according to internal and external requirements. - Support regulatory inspections and audits by providing necessary documentation and expertise. - Collaborate with product development, quality assurance, and marketing teams to align regulatory strategies with business goals. - Serve as the primary contact for regulatory agency inquiries and facilitate communication with internal stakeholders. Qualifications: Required: - Bachelor's degree in Life Sciences, Regulatory Affairs, or a related field. - Minimum 2-8 years of experience in regulatory affairs within the healthcare or pharmaceutical industry. - In-depth knowledge of regulatory requirements and guidelines. - Strong analytical skills for interpreting complex regulatory documents and data. Preferred: - Master's degree in a relevant field. - Experience with medicines and formulations products. Additional Details: Medyur Pharmaceuticals Limited offers cell phone and internet reimbursement as benefits. The job type is full-time and permanent with day shift schedules. Performance bonuses are provided based on achievements. The company prefers candidates who can reliably commute or plan to relocate to Faridabad, Haryana. The work location is in person. Technical Skills: - Proficiency in regulatory submission software and electronic document management systems. - Strong understanding of risk management principles and methodologies. - Familiarity with project management tools for timely delivery of regulatory submissions. Soft Skills: - Exceptional verbal and written communication skills to convey complex regulatory concepts. - Strong organizational skills and attention to detail for accuracy in regulatory submissions. - Proactive approach and ability to work independently and collaboratively in a team environment. - Adaptability and resilience in a fast-paced regulatory landscape. Experience: - Required 2 years of experience in drug regulatory affairs. Language: - English proficiency is preferred. As a Drug Regulatory Affairs Specialist at Medyur Pharmaceuticals Limited, you will be responsible for ensuring compliance with regulatory requirements for our products and driving successful product launches. You will collaborate with cross-functional teams to maintain regulatory compliance and facilitate smooth communication with regulatory bodies. Key Responsibilities: - Prepare and submit regulatory documentation such as dossiers for pre-market submissions to obtain necessary approvals. - Stay up to date on current regulatory requirements, guidelines, and industry trends in global markets. - Develop and maintain strong relationships with regulatory bodies to support approvals. - Review changes to regulatory policies and recommend actions for continued compliance. - Conduct regulatory impact assessments to evaluate potential changes affecting product development. - Maintain regulatory files, records, and reports according to internal and external requirements. - Support regulatory inspections and audits by providing necessary documentation and expertise. - Collaborate with product development, quality assurance, and marketing teams to align regulatory strategies with business goals. - Serve as the primary contact for regulatory agency inquiries and facilitate communication with internal stakeholders. Qualifications: Required: - Bachelor's degree in Life Sciences, Regulatory Affairs, or a related field. - Minimum 2-8 years of experience in regulatory affairs within the healthcare or pharmaceutical industry. - In-depth knowledge of regulatory requirements and guidelines. - Strong analytical skills for interpreting complex regulatory documents and data. Preferred: - Master's degree in a relevant field. - Experience with medicines and formulations products. Additional Details: Medyur Pharmaceuticals Limited offers cell phone and internet reimbursement as benefits. The job type is full-time and permanent with day shift schedules. Performance bonuses are provided based on achievements. The company prefers candidates who can reliably commute or pla

As a Regulatory Operations Assistant, your role will involve supporting daily operational activities within Regulatory Operations for preparing regulatory submissions required to market pharmaceutical products in domestic and international markets. You will be responsible for maintaining systems to ensure compliance with electronic submission requirements and document management systems. Additionally, you will lead and support the creation, implementation, and maintenance of departmental Standard Operating Procedures (SOPs), Work Instructions (WIs), and operational processes in alignment with regulatory requirements and best practices. Key Responsibilities: - Serve as a seasoned regulatory operations professional with a comprehensive understanding of global submission requirements and processes, applying problem-solving skills to resolve technical and operational issues. - Manage end-to-end preparation, compilation, publishing, quality control, validation, and delivery of electronic regulatory submissions (eCTD) in compliance with global Health Authority requirements and internal standards. - Support submission planning and execution for initial marketing applications and post-approval lifecycle submissions across multiple regions including the U.S., Canada, EU, and Asia-Pacific. - Collaborate cross-functionally with various stakeholders to ensure timely and accurate handoff of components for inclusion in submissions. - Lead and contribute to the development, revision, implementation, and training of departmental SOPs, WIs, and standardized publishing processes. - Assist in managing and improving templates, procedures, and tools used for global submission activities. - Troubleshoot technical issues related to publishing tools and document formatting, supporting resolution of validation errors. - Participate in evaluating and implementing new regulatory technologies to support transitions to electronic platforms. - Maintain compliant archival and storage of regulatory documents in alignment with regulatory and business needs. - Mentor junior staff, provide publishing guidance, and act as a resource for complex submissions. Qualifications Required: - Bachelor's Degree required; Advanced Degree desirable - Minimum five (5) years of regulatory operations experience in the pharmaceutical or biotechnology industry - Proven expertise in preparation, compilation, publishing, and validation of eCTD submissions - In-depth knowledge of electronic publishing tools, Regulatory Information Management systems, and document management systems - Strong understanding of global regulatory submission guidance - Excellent organizational, time management, and communication skills - Experience with electronic submissions, specifically eCTD - Understanding of document management processes in a regulated pharmaceutical environment - Experience in developing, revising, and maintaining SOPs, WIs, and internal processes The above role will require you to have a strong background in regulatory operations, experience with global regulatory submissions, and proficiency in electronic publishing tools and document management systems. Your attention to detail, problem-solving skills, and ability to collaborate effectively across teams will be essential for success in this role. As a Regulatory Operations Assistant, your role will involve supporting daily operational activities within Regulatory Operations for preparing regulatory submissions required to market pharmaceutical products in domestic and international markets. You will be responsible for maintaining systems to ensure compliance with electronic submission requirements and document management systems. Additionally, you will lead and support the creation, implementation, and maintenance of departmental Standard Operating Procedures (SOPs), Work Instructions (WIs), and operational processes in alignment with regulatory requirements and best practices. Key Responsibilities: - Serve as a seasoned regulatory operations professional with a comprehensive understanding of global submission requirements and processes, applying problem-solving skills to resolve technical and operational issues. - Manage end-to-end preparation, compilation, publishing, quality control, validation, and delivery of electronic regulatory submissions (eCTD) in compliance with global Health Authority requirements and internal standards. - Support submission planning and execution for initial marketing applications and post-approval lifecycle submissions across multiple regions including the U.S., Canada, EU, and Asia-Pacific. - Collaborate cross-functionally with various stakeholders to ensure timely and accurate handoff of components for inclusion in submissions. - Lead and contribute to the development, revision, implementation, and training of departmental SOPs, WIs, and standardized publishing processes. - Assist in managing and improving templates, procedures, and tools used for global submission activit

As an A&R Scout / Artist Relations Assistant at Ice Cream Music Records Ltd, you will be instrumental in discovering emerging EDM talent and supporting the labels artist development pipeline. Your role will involve identifying, evaluating, and recommending upcoming EDM artists, producers, and DJs for potential signing. You will review and assess demo submissions, maintain relationships with artists and industry professionals, and collaborate with internal teams on campaign strategies and release schedules. Key Responsibilities: - Identify, evaluate, and recommend upcoming EDM artists, producers, and DJs for potential signing. - Review and assess demo submissions to determine artistic and commercial potential. - Maintain and strengthen relationships with artists, managers, and producers. - Support the A&R department with contractual coordination, artist onboarding, and release planning. - Collaborate with the marketing and creative teams on campaign strategies and release schedules. - Monitor music trends, emerging genres, and social platforms to identify potential opportunities. - Assist in organizing listening sessions, showcases, and other artist-related events. Qualifications: - Strong knowledge of EDM and the electronic music industry, including key artists, labels, and market trends. - Excellent verbal and written communication skills. - Demonstrated ability to identify talent and understand artistic potential. - Prior experience in A&R, artist management, or a related music industry role preferred. - Familiarity with digital music distribution and analytics platforms (Spotify for Artists, Apple Music for Artists, etc.). - Self-motivated, organized, and able to manage multiple projects simultaneously. Join Ice Cream Music Records Ltd to work within a growing international label with expanding global partnerships. You will have exposure to industry professionals, artist management, and creative marketing teams in a collaborative environment that encourages innovation, initiative, and professional growth. Competitive compensation will be offered based on experience and performance. Shape the next generation of global EDM talent with us.,

As a Hardware Engineer at Qualcomm India Private Limited, you will be part of a leading technology innovator that pushes the boundaries to enable next-generation experiences and drive digital transformation for a smarter, connected future. Your role will involve planning, designing, optimizing, verifying, and testing electronic systems, circuits, mechanical systems, and various other cutting-edge technologies to launch world-class products. Collaboration with cross-functional teams will be essential to develop solutions and meet performance requirements. **Key Responsibilities:** - Front-End implementation of MSIP (Temp/Voltage/Security Sensors, Controllers) designs - RTL development and validation for linting, clock-domain crossing, low power, and DFT rules - Test-plan development and debug in collaboration with the verification team - Timing constraints development, synthesized netlist delivery, and support for PD STA - UPF writing, power-aware equivalence checks, and low power checks - DFT insertion and ATPG analysis for optimal SAF, TDF coverage - Support SoC integration and chip level pre/post-silicon debug **Qualifications Required:** - Bachelor's degree in Computer Science, Electrical/Electronics Engineering, Engineering, or related field with 2+ years of Hardware Engineering experience - OR Master's degree in Computer Science, Electrical/Electronics Engineering, Engineering, or related field with 1+ year of Hardware Engineering experience - OR PhD in Computer Science, Electrical/Electronics Engineering, Engineering, or related field **Skills & Experience:** - MTech/BTech in EE/CS with hardware engineering experience of 3+ years - Experience in micro-architecture development, RTL design, front-end flows (Lint, CDC, low-power checks, etc.), synthesis/DFT/FV/STA - Experience with post-silicon bring-up and debug is a plus - Ability to work with global teams and possess excellent communication skills Qualcomm is an equal opportunity employer and is committed to providing accessible processes for individuals with disabilities. If you require accommodations during the application/hiring process, please contact disability-accommodations@qualcomm.com or Qualcomm's toll-free number. It is expected that all employees abide by applicable policies and procedures, including security and confidentiality requirements. Please note that Qualcomm does not accept unsolicited resumes or applications from agencies. Staffing and recruiting agencies are not authorized to use the Qualcomm Careers Site for submissions. For more information about this role, contact Qualcomm Careers directly.,

As a Qualcomm Hardware Engineer, you will be responsible for planning, designing, optimizing, verifying, and testing electronic systems, circuits, mechanical systems, and various digital/analog/RF/optical systems. You will work on cutting-edge products and collaborate with cross-functional teams to meet performance requirements. **Key Responsibilities:** - Strong designer who can work independently on peripheral IPs - Develop design and microarchitecture solutions - Guide and mentor junior team members - Engage with external teams to drive and resolve cross-team dependencies - Take complete responsibility for one or more projects - Ability to make schedule estimates is a plus - People management experience is a plus **Qualifications Required:** - Bachelor's degree in Computer Science, Electrical/Electronics Engineering, or related field with 3+ years of Hardware Engineering experience - OR Master's degree in Computer Science, Electrical/Electronics Engineering, or related field with 2+ years of Hardware Engineering experience - OR PhD in Computer Science, Electrical/Electronics Engineering, or related field with 1+ year of Hardware Engineering experience **Skills & Requirements:** - 4-8 years of work experience in ASIC IP cores design - Bachelor's in Electrical Engineering required; Master's preferred - Knowledge of AMBA protocols such as AXI, AHB, APB, SoC clocking/reset/debug architecture, and peripherals like USB/PCIE/Ethernet preferred - Hands-on experience in Low power design and Multi Clock designs - Experience in using ASIC development tools like Lint, CDC, Design compiler, and Primetime - Strong experience in micro-architecting RTL design - Excellent problem-solving, communication, and teamwork skills - Self-driven and able to work with minimum supervision - Familiarity with System Verilog, Verilog, C/C++, Perl, and Python is a plus - Ability to lead a small design team **About Qualcomm:** Qualcomm is committed to providing accessible processes for individuals with disabilities during the application/hiring process. They offer reasonable accommodations to support individuals with disabilities to participate in the hiring process. Qualcomm expects its employees to abide by all applicable policies and procedures, including security measures for protecting confidential information. Staffing and Recruiting Agencies are advised that Qualcomm's Careers Site is for individuals seeking jobs directly at Qualcomm, and unsolicited submissions will not be accepted. For more information about this role, please reach out to Qualcomm Careers.,

As a Software Engineer at Qualcomm India Private Limited, you will be involved in designing, developing, modifying, and validating embedded and cloud edge software, applications, and specialized utility programs. Your role will focus on launching cutting-edge products that exceed customer expectations by collaborating with various teams to design system-level software solutions and gather performance requirements. **Key Responsibilities:** - Develop and execute detailed test plans and test cases for video surveillance applications on edge platforms. - Conduct manual functional, integration, and system-level testing across diverse hardware and software configurations. - Identify, document, and track defects, working closely with development teams for resolution. - Validate video streaming quality, latency, and analytics accuracy under varying network and environmental conditions. - Ensure comprehensive test coverage and timely delivery by collaborating with cross-functional teams. - Analyze test results, identify gaps, and recommend process and tool improvements. **Qualification Required:** - Bachelor's or Master's degree in Computer Science, Electronics, or a related field. - 3+ years of experience in manual testing, preferably in video surveillance or multimedia systems. - Familiarity with Linux-based systems, networking concepts, and debugging tools. - Strong analytical and problem-solving skills. - Proficiency in Linux commands and familiarity with Python. **Note:** Although the current focus is on manual testing, there may be opportunities to contribute to test automation initiatives in the future. **Preferred Skills:** - Hands-on experience with test management tools like JIRA and TestRail. - Ability to perform stress, load, and endurance testing manually and via automation scripts. - Understanding of video streaming protocols (RTSP, RTP) and edge device solutions. *Applicants:* Qualcomm is an equal opportunity employer. For individuals with disabilities needing accommodations during the application/hiring process, Qualcomm is committed to providing accessible support. Reach out to disability-accommodations@qualcomm.com for assistance. Qualcomm also ensures workplace accessibility for individuals with disabilities. *Company Policy:* Qualcomm expects employees to adhere to all applicable policies and procedures, including security and confidentiality requirements. Compliance with these policies is mandatory. *Recruitment Notice:* The Qualcomm Careers Site is exclusively for individuals seeking employment at Qualcomm. Staffing agencies and represented individuals are not permitted to use this site for submissions. Unsolicited resumes or applications from agencies will not be accepted. For more information about roles, please contact Qualcomm Careers.,

As a Sales Manager at Good Enough Energy Pvt. Ltd., you will be responsible for driving Battery Energy Storage Systems (BESS) and renewable energy solutions in the B2B sector. Your role will involve contributing to market growth, strategic account management, and business expansion across utility scale and grid scale. Key Responsibilities: - Sales & Business Development: - Drive BESS sales in the Grid Scale / Utility Scale Market - Identify and secure new business opportunities - Account & Client Management: - Build long-term relationships with key clients and partners - Oversee the client lifecycle from lead generation to contract administration - Bidding & Tender Management: - Lead bid/tender submissions for large projects - Prepare pre-qualification documents and present company credentials - Generate enquiries, prepare proposals, and negotiate contracts - Contract Management: - Finalize contracts and manage post-award administration - Ensure compliance and manage contract amendments - Business Expansion & Vendor Management: - Support expansion into solar, wind, and water segments - Manage vendor approvals with major developers - Strategic Planning & Execution: - Contribute to company vision, values, and strategic planning - Implement business plans and optimize product management processes - Performance Management: - Monitor market performance and recommend improvements - Ensure effective sales and marketing execution Desired Skills & Qualifications: - Any Degree in electrical / electronic or power engineering or mechanical engineering / MBA - Experience in Grid Scale / Utility Scale (energy/renewables preferred) - Strong skills in strategic account management and business development - Expertise in proposal drafting and contract negotiations - Excellent client relationship and vendor management - Experienced in strategic planning, budgeting, and execution - Effective communication, presentation, and negotiation abilities - Collaborative and growth-oriented mindset,

As a Medical Coder at our company in Noida, India, you will be responsible for analyzing medical records and documentation to identify services provided during patient evaluations and management. Your key responsibilities will include: - Assigning appropriate E&M codes based on the level of service rendered and in accordance with coding guidelines and regulations (e.g., CPT, ICD-10-CM, HCPCS) - Ensuring coding accuracy and compliance with coding standards, including documentation requirements for various E&M levels - Staying up-to-date with relevant coding guidelines, including updates from regulatory bodies (e.g., Centers for Medicare and Medicaid Services, American Medical Association) - Adhering to coding regulations, such as HIPAA (Health Insurance Portability and Accountability Act) guidelines, to ensure patient privacy and confidentiality - Following coding best practices and maintaining a thorough understanding of coding conventions and principles - Collaborating with healthcare professionals, including physicians, nurses, and other staff members, to obtain necessary information for coding purposes - Communicating with providers to address coding-related queries and clarify documentation discrepancies - Working closely with billing and revenue cycle teams to ensure accurate claims submission and facilitate timely reimbursement - Conducting regular audits and quality checks on coded medical records to identify errors, inconsistencies, or opportunities for improvement - Participating in coding compliance programs and initiatives to maintain accuracy and quality standards To be considered for this position, you need to meet the following qualification criteria: - Certified Professional Coder (CPC) or equivalent coding certification (e.g., CCS-P, CRC) - In-depth knowledge of Evaluation and Management coding guidelines and principles - Proficient in using coding software and Electronic Health Record (EHR) systems - Familiarity with medical terminology, anatomy, and physiology - Strong attention to detail and analytical skills - Excellent communication and interpersonal skills - Ability to work independently and as part of a team - Compliance-oriented mindset and understanding of healthcare regulations - Strong organizational and time management abilities - Continuous learning mindset to stay updated on coding practices and changes,

You will be responsible for analyzing medical records and documentation to identify services provided during patient evaluations and management. Your main task will be to assign appropriate E&M codes based on the level of service rendered and in accordance with coding guidelines and regulations such as CPT, ICD-10-CM, and HCPCS. It is crucial to ensure coding accuracy and compliance with coding standards, including documentation requirements for various E&M levels. Staying up-to-date with relevant coding guidelines, including updates from regulatory bodies like the Centers for Medicare and Medicaid Services and the American Medical Association, is essential. Adherence to coding regulations, such as HIPAA guidelines, is necessary to ensure patient privacy and confidentiality. Following coding best practices and maintaining a thorough understanding of coding conventions and principles are also key aspects of the role. - Collaboration with healthcare professionals, including physicians, nurses, and other staff members, is required to obtain necessary information for coding purposes. - You will need to communicate with providers to address coding-related queries and clarify documentation discrepancies. - Working closely with billing and revenue cycle teams to ensure accurate claims submission and facilitate timely reimbursement is part of the job responsibilities. - Conducting regular audits and quality checks on coded medical records to identify errors, inconsistencies, or opportunities for improvement is also a key aspect of the role. - Participation in coding compliance programs and initiatives to maintain accuracy and quality standards is expected. To be considered for this position, applicants need to meet the following qualification criteria: - Certified Professional Coder (CPC) or equivalent coding certification (e.g., CCS-P, CRC) - In-depth knowledge of Evaluation and Management coding guidelines and principles - Proficient in using coding software and Electronic Health Record (EHR) systems - Familiarity with medical terminology, anatomy, and physiology - Strong attention to detail and analytical skills - Excellent communication and interpersonal skills - Ability to work independently and as part of a team - Compliance-oriented mindset and understanding of healthcare regulations - Strong organizational and time management abilities - Continuous learning mindset to stay updated on coding practices and changes,

As an experienced NPI Manager, you will be responsible for coordinating with R&D New Products Development groups to develop strategies for new products and provide engineering support throughout the product development process. Key Responsibilities: - Proficient in Microsoft Office applications (Excel, Word, PowerPoint) for effective project management and documentation. - Ability to handle a team of NPI Engineers & oversee the New Product Introduction process. - Hands-on experience with Gerbers and related tools, including interpretation of electronic components datasheets, wave pallets, Routing pallet & test fixture development. - Conduct product testing and possess awareness and experience in using testing tools like Multimeter, CRO, etc. Qualifications Required: - Minimum of 2-4 years of experience in the same domain. - Qualification B.Tech. The company is looking for a candidate who can effectively coordinate with R&D for New Product Development strategies, provide engineering support for all activities in the product development process, prepare project timelines, assess resource requirements, and evaluate financials for manufacturing processes. You will also be responsible for monitoring the status of all new products, ensuring effective project execution in compliance with policies, procedures, and regulations, and preparing plans for NPI projects to deliver high-quality products. Additionally, you will collaborate with engineering and product management departments to develop and implement Manufacturing Plans, assist the Manufacturing department in ensuring effective communication across all departments, and administer first release products for D&D submission to regulatory bodies. Furthermore, you will assist in the integration of all products according to the product lifecycle, ensure compliance with ECO procedures and work instructions, and provide technical support to the Materials Management team for RFP initiatives. Your role will also involve developing prototype designs following required techniques and manufacturing processes, maintaining an inventory, and ensuring the availability of required equipment, tools, test equipment, and prototype parts. You will analyze and recommend improvements to production processes for cost reduction and quality improvement, as well as coordinate with senior management, providing regular updates on product status through appropriate reports. Preferred Skills: - Experience in managing teams. - Knowledge of manufacturing processes and compliance. As an experienced NPI Manager, you will be responsible for coordinating with R&D New Products Development groups to develop strategies for new products and provide engineering support throughout the product development process. Key Responsibilities: - Proficient in Microsoft Office applications (Excel, Word, PowerPoint) for effective project management and documentation. - Ability to handle a team of NPI Engineers & oversee the New Product Introduction process. - Hands-on experience with Gerbers and related tools, including interpretation of electronic components datasheets, wave pallets, Routing pallet & test fixture development. - Conduct product testing and possess awareness and experience in using testing tools like Multimeter, CRO, etc. Qualifications Required: - Minimum of 2-4 years of experience in the same domain. - Qualification B.Tech. The company is looking for a candidate who can effectively coordinate with R&D for New Product Development strategies, provide engineering support for all activities in the product development process, prepare project timelines, assess resource requirements, and evaluate financials for manufacturing processes. You will also be responsible for monitoring the status of all new products, ensuring effective project execution in compliance with policies, procedures, and regulations, and preparing plans for NPI projects to deliver high-quality products. Additionally, you will collaborate with engineering and product management departments to develop and implement Manufacturing Plans, assist the Manufacturing department in ensuring effective communication across all departments, and administer first release products for D&D submission to regulatory bodies. Furthermore, you will assist in the integration of all products according to the product lifecycle, ensure compliance with ECO procedures and work instructions, and provide technical support to the Materials Management team for RFP initiatives. Your role will also involve developing prototype designs following required techniques and manufacturing processes, maintaining an inventory, and ensuring the availability of required equipment, tools, test equipment, and prototype parts. You will analyze and recommend improvements to production processes for cost reduction and quality improvement, as well as coordinate with senior management, providing regular updates on product status through appropriate reports. Preferred Skill

As an Underwriting Assistant I at Everest's Property and Casualty Division, your role involves managing and processing an assigned portfolio of business. Your responsibilities include: - Reviewing incoming transactions and related information for completeness, accuracy, and quality. - Processing multi-line new business submissions, renewal submissions, and endorsements, including rating, policy construction, and assembly in a timely and accurate manner. - Regularly reviewing and adhering to department processing guidelines and procedures to ensure accuracy. - Managing underwriting relationships with timely responses to service inquiries. - Maintaining all correspondence activity with internal and external customers, including daily diaries on pending transactions. - Ensuring compliance with ODEN state rules and regulations regarding cancellations and reinstatements. - Gathering underwriting information, such as experience reports, final audits, loss control reports, financial reports, loss runs, MVRs, and FEINs. - Handling special projects as needed. Competencies required for this role include: - Strong desk management, written, and verbal communication skills. - Ability to multitask, independently organize work, and prioritize competing demands and requests to complete work within required time constraints. - Strong analytical skills and mathematical aptitude. - Knowledge of underwriting principles, product-specific coverage, policy forms, pricing tools, regulatory compliance, and insurance systems. - Proficiency in using online reference manuals and effectively using multiple electronic systems. - Ability to work in a team environment and handle multiple deadlines.,

As a Sales Manager at Good Enough Energy Pvt. Ltd., you will be responsible for driving Battery Energy Storage Systems (BESS) and renewable energy solutions in the B2B sector. Your key responsibilities will include: - Sales & Business Development: - Drive BESS sales in the Grid Scale / Utility Scale Market - Identify and secure new business opportunities - Account & Client Management: - Build long-term relationships with key clients and partners - Oversee the client life cycle from lead generation to contract administration - Bidding & Tender Management: - Lead bid/tender submissions for large projects - Prepare pre-qualification documents and present company credentials - Generate enquiries, prepare proposals, and negotiate contracts - Contract Management: - Finalise contracts and manage post-award administration - Ensure compliance and manage contract amendments - Business Expansion & Vendor Management: - Support expansion into solar, wind, and water segments - Manage vendor approvals with major developers - Strategic Planning & Execution: - Contribute to the company vision, values, and strategic planning - Implement business plans and optimize product management processes - Performance Management: - Monitor market performance and recommend improvements - Ensure effective sales and marketing execution Qualifications Required: - Any Degree in electrical/electronic or power engineering, or mechanical engineering / MBA - Experience in Grid Scale / Utility Scale (energy/renewable preferred) - Strong skills in strategic account management and business development - Expertise in proposal drafting and contract negotiations - Excellent client relationship and vendor management - Experienced in strategic planning, budgeting, and execution - Effective communication, presentation, and negotiation abilities - Collaborative and growth-oriented mindset Join Good Enough Energy Pvt. Ltd. to be a part of India's first and most advanced manufacturer of Battery Energy Storage Systems and contribute to the transition to a greener, cleaner future.,

As a Medical Summary Specialist, your role involves producing concise and accurate clinical summaries from various medical records within defined SLAs. Your key responsibilities will include: - Extracting and structuring key clinical elements such as diagnoses, medications, procedures, labs, and follow-up plans into standardized summary templates. - Validating clinical facts, reconciling discrepancies, and flagging ambiguities for clinician clarification. - Applying ICD-10/SNOMED conventions to ensure diagnostic and procedural alignment. - Operating EHR platforms and transcription/NLP tools to accelerate summarization while maintaining quality and data security standards. - Adhering to data privacy and compliance protocols (HIPAA/GDPR) and contributing to continuous improvement initiatives for summarization quality. In order to excel in this role, you must have: Must-Have: - Strong command of medical terminology and clinical workflows across specialties. - Familiarity with ICD-10 and SNOMED conventions. - Hands-on experience with Electronic Health Record systems and medical transcription tools. - Knowledge of HIPAA and data protection practices. - Ability to work accurately under SLA-driven workflows. Preferred qualifications include: - Certification in clinical coding or health information management. - Experience using clinical NLP/AI-assisted summarization platforms. - Previous on-site experience supporting US/EU-based clinical customers or regulatory submissions. The company offers a collaborative and clinically-focused on-site team with structured training and QA support. You can expect clear career pathways into senior clinical documentation, coding, or quality roles within healthcare operations. Competitive compensation and benefits are aligned to role and market standards. In your application, highlight examples of past medical summaries or documentation audits, and list EHR/tools you have used. Detail-oriented clinical documentation professionals who deliver high-quality summaries are sought to improve care continuity and downstream clinical workflows.,

As a Qualcomm Hardware Engineer, you will be responsible for planning, designing, optimizing, verifying, and testing electronic systems, including circuits, mechanical systems, Digital/Analog/RF/optical systems, test systems, and more to launch cutting-edge products. You will collaborate with cross-functional teams to develop solutions and meet performance requirements. Key Responsibilities: - Develop a deep understanding of 3-D Graphics hardware pipeline, feature sets, data paths, block functionalities & interfaces - Strategize, brainstorm, and propose a DV environment, develop test bench, own test plan, debug all RTL artefacts, and achieve all signoff matrices - Engage with EDA vendors, explore new DV methodologies, and collaborate with worldwide teams to achieve project goals Qualifications Required: - Bachelor's degree in Computer Science, Electrical/Electronics Engineering, or related field with 4+ years of Hardware Engineering experience - OR Master's degree with 3+ years of Hardware Engineering experience - OR PhD with 2+ years of Hardware Engineering experience As a GPU Functional Verification Engineer at Qualcomm, you will work on various project responsibilities, including developing UVM/SV based constrained random test bench for functional verification, subsystem level TB for complete GPU workload analysis, emulation platforms for performance analysis, and more. Strong communication skills, proficiency with formal tools, and the ability to learn, improve, and deliver are essential for this role. Qualcomm is an equal opportunity employer committed to providing accessible processes for individuals with disabilities. If you require accommodations during the application/hiring process, you can contact Qualcomm at disability-accommodations@qualcomm.com or through the toll-free number provided on the website. Qualcomm expects its employees to adhere to all applicable policies and procedures, including security and confidentiality requirements for protecting company information. Please note that Qualcomm's Careers Site is for individuals seeking jobs directly at Qualcomm. Staffing agencies and individuals represented by agencies are not authorized to use the site for submissions. Unsolicited resumes or applications from agencies will not be accepted. For more information about the role, you can reach out to Qualcomm Careers directly.,