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Job Description : SUMMARY: The Medical Surgery Coder will play a key role in reviewing and analyzing medical billing and coding for processing. The Medical Surgery Coder will review and accurately code ambulatory surgical procedures for reimbursement. SPECIFIC KNOWLEDGE REQUIRED: Required certification in one of the following : CPC, RHIA, RHIT Minimum of 2 years acute care coding experience of all patient types Surgical, Outpatient, Inpatient, SDS and ER, with strong experience in Inpatient. Successful completion of formal education in basic ICD-9-CM/ICD-10/CPT coding, medical terminology, anatomy/physiology and disease process. Knowledge of computers and Windows-driven software Excellent command of written and spoken English Cooperative work attitude toward and with co-employees, management, patients, outside contacts Ability to promote favourable company image with patients, insurance companies, and public. Ability to solve problems associated with assigned task ADDITIONAL SKILLS REQUIRED/PREFERRED: Obtain operative reports Obtain implant invoices, implant logs, and pathology reports as applicable Supports the importance of accurate, complete and consistent coding practices to produce quality healthcare data. Adheres to the ICD-9/ICD-10 coding conventions, official coding guidelines approved by CPT, AMA, AAOS, and CCI. Uses skills and knowledge of the currently mandated coding and classification systems, and official resources to select the appropriate diagnostic and procedural codes. Assigns and reports the codes that are clearly supported by documentation in the health record. Consults physicians for clarification and additional documentation prior to code assignment when there is conflicting or ambiguous data in the health record. Strives for the optimal payment to which the facility is legally entitled. Assists and educates physicians and other clinicians by advocating proper documentation practices. Maintains and continually enhances coding skills. Coders need to be aware of changes in codes, guidelines, and regulations. They are required to maintain 90% or above coding accuracy average. Codes a minimum of 50 cases on a daily basis. Assures accurate operative reports by checking spelling, noting omissions and errors and returning to transcription for correction. Codes all third party carriers and self- pay cases equitably for patient services and supplies provided. Adheres to OIG guidelines which include: Diagnosis coding must be accurate and carried to the highest level of specificity. Claim forms will not be altered to obtain a higher amount. All coding will reflect accurately the services provided and cases reviewed for the possibility of “unbundling”, “up-coding” or down coding.” Coders may be involved in denials of claims for coding issues. Some centers require a code disagree form be completed. Coders are required to provide their supporting documentation to be presented to the center for approval. (Surg Centers call this a coding variance) Ensures the coding site specifics are updated as needed for each center assigned. Identifies and tracks all cases that are not able to be billed due to lacking information such as operative notes, path reports, supply information etc. On a weekly/daily basis provide a documented request to the center requesting the information needed. Responsible for properly performing month end tasks within the established timeframe including running month end reports for each center assigned and tracking of cases that are not yet billed for the month. Cases will be reviewed as part of an in-house audit process to ensure quality and accuracy of claims. Corrections may be needed after review. Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time PHYSICAL REQUIREMENTS: Requires ability to use a telephone Requires ability to use a computer Department Development Open Positions 1 Skills Required Surgery Coding Location Hyderabad, Telangana, India Years Of Exp 3 to 7 years Posted On : 05-Jun-2025

Description 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. Brief Job Overview This is a non-supervisory position in Store, to facilitate the entire Store operations and Inventory Management in the Laboratory How will YOU create impact here at USP? Responsible for the daily operations of USP India Main site Chemical store and Non-Lab stores including the receiving the Chemicals and arranging them in the chemical stores as per the compatibility lists, SOPs requirements and material movement activities for the Unit-II. Responsible for maintaining ERP-Inventory module, to support the Inventory Management activities and responsible for daily/Weekly cycle counts of the Inventory items in ERP. Receiving all materials and ensuring the quantity and physical inspection and if any shortcomings found report immediately to purchase department for rectifications. Responsible for Min-Max planning in ERP Inventory module Responsible to maintain end to end tracking of chemicals in APEX software Responsible for creation of Purchase requisitions Responsible for receipts and issuing of materials to different departments like CLO, RSL, R&D, Synthetic and Biologics in ERP module. Responsible for generation of ERP reports and documenting it. To maintain SDS database for the chemicals available in the Chemical Stores. To segregate the expired chemicals and work for the disposal of chemicals in coordination with the Safety team. To maintain the records for Disposal activities. To conduct the periodic physical stock verification in Stores. To ensure safety practices are followed in the Stores Responsible for invoices submission to purchase department for accounting. To take up the additional responsibilities assigned by the supervisor. 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 Inventory control specialist Bachelors in Science (B.Sc.,/ B.Pharm) with 3-6 years’ working in chemical stores/warehouse with knowledge of ERP/SAP system or any other Inventory management system. Must have knowledge on handling and storage of chemicals Inventory control Associate Bachelors in Science (B.Sc.,/ B.Pharm) with 1-3 years’ working in chemical stores/warehouse with knowledge of ERP/SAP system or any other Inventory management system. Must have knowledge on handling and storage of chemicals Additional Desired Preferences Thorough knowledge of all Warehouse functions. Knowledge on compliance, and Logistic etc. Knowledge on ERP system Knowledge on handling and storage of chemicals Knowledge on Laboratory compliance (GMP and GLP). 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. Job Category Sales & Marketing Job Type Full-Time Show more Show less

Description 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. Brief Job Overview This is a hands-on, non-supervisory, non-laboratory role in the India Biologics department. The incumbent work collaboratively in the reference standard/ARM development program within the Global Biologics department. The incumbent will participate in the development of replacement and new reference standards /ARM in support of USP’s mission and core business. The incumbent will also focus on supporting the suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports to assist in 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 timely 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) Has The Following Responsibilities Roles and Responsibilities Maintain smooth collaboration and works closely with key stakeholders across the globe to develop reference standards for biotechnology pharmaceutical products including proteins, peptides, heparins, antibiotics, and advanced therapies. Works to draft protocols, reports and address scientific and technical queries from internal and external stakeholders in timely manner pertaining to reference standards/ARMs Oversees and facilitates the development of standards and solutions to address analytical challenges associated with biological medicines. Supports day to day operations of the Stability (CSU) program covering the USP Biologics RS catalog inventory. Reviews RS testing history and drafts test protocols for collaborative studies and CSU studies and submits to labs based on designated testing requirements and schedules. Liaisons and Assists laboratories to ensure collaborative testing/CSU testing is completed accurately 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 current and historical Stability testing data assessment and prepare stability trend reports. Maintains and updates 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, Quality Assurance and Reference Standard Evaluation with 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 Reviews protocols and/or reports of other Scientists as assigned by manager. Who is USP Looking For? Preferred Qualifications 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: 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. Sr. Scientist I Ph.D. degree in Biochemistry, Analytical Chemistry or Biological Sciences . Minimum of 7 to 10 years of post-educational work experience in recombinant therapeutic proteins, peptides and carbohydrates. in Biochemistry, or Biological Sciences with minimum of 11 to 13 years of commensurate industrial experience. 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. Job Category Chemistry & Scientific Standards Job Type Full-Time Show more Show less

(NOTE: HCC CODERS NOT ELIGIBLE FRESHERS NO OPENINGS) OPENING > Denial Certified ( CHN / CBE & PUNE) Temporary work from home available > Surgery Certified ( CHN / CBE & PUNE) Temporary work from home available > EM Certified ( CHN / CBE ) Temporary work from home available only for chennai > ED Facility Certified ( CHN / CBE & PUNE) Temporary work from home available > Radiology Certified ( CHN / CBE & PUNE) Only work from office Roles and Responsibilities: * Candidates should have minimum 1+ year of experience into medical coding * Any certification is mandatory * If candidate is having any training exposure its added advantage * Looking strong domain knowledge in Medical coding * Salary is not a constraint * Good communication * Location : Chennai / Coimbatore /Pune *Day Shift Interested Candidate Can Send Resume # HR SAMEEMA - 7339689430

We Are Hiring: Same Day Surgery Coders (Certified Only) Company: MedMetrix Work Mode: Work From Office (No Remote Option) Experience: Minimum 1+ Year Required Specialty: Same Day Surgery Joining: Immediate Joiners Preferred We are looking for experienced and certified medical coders with a background in Same Day Surgery to join our team. Mode of Interview: Walk-in Salary: As per market standards (Negotiable based on experience) Eligibility: Certified Coders only with a minimum of 1 year of experience in Same Day Surgery Work Mode: Work from Office only Address: :7th Floor , Millenia Business Park II, 4A Campus,143 , Dr. M.G.R. Road, Kandanchavadi, Perungudi,Chennai, Tamil Nadu 600096, India Interested candidates can call and schedule their interview with: Ranjitha (HR) 8807618852 ( Whatsapp and Call )

Job Description In This Role, Your Responsibilities Will Be: Develop, maintain, and update operator manuals and instruction sheets for Professional Tools products. Format documents and create artwork using Adobe tools (Illustrator, InDesign, Photoshop). Design and update product warning labels and markings. Ensure compliance with internal and external standards (ANSI, UL, ISO, UL/IEC 62841, UL/IEC 60335). Interpret product functionality and risk without direct access to physical products. Collaborate with cross-functional teams including Product Design, Manufacturing, Marketing, and Service across global locations. Gather technical content from various sources such as existing manuals, product drawings, and standards. Maintain consistency in terminology, formatting, and structure across all documentation. Support Product Environmental Compliance (PEC) by creating and updating documents like Prop 65, REACH, RoHS, and SDS files. Assist in regulatory documentation including Technical Files and certification markings (CE, RCM). Continuously explore new tools and practices to enhance documentation quality. Adhere to and document internal documentation standards. Who You Are: Emerson’s global Professional Tools business offers the broadest portfolio of reliable tools, connected equipment and software technologies for those working in mechanical, electrical and plumbing trades. This role is responsible for content writing, artwork creation, and material compliance of user documents for low-risk use of these products. For This Role, You Will Need: Bachelor’s degree with Science or Engineering background. 3 to 5 years of experience in technical writing, preferably in a product-based environment. Proficiency in Adobe Acrobat tools (Illustrator, InDesign, Photoshop) and Microsoft Office Suite. Strong writing and editing skills tailored for a global audience. Strong communication skills and ability to convey complex information clearly. Ability to interpret engineering drawings and technical data. Self-motivated, detail-oriented, and results-driven Preferred Qualifications that Set You Apart: Bachelor’s degree in Mechanical or Electrical Engineering will be preferred. Post graduate Diploma in technical writing will be added advantage. Familiarity with CAD tools (SolidWorks or Solid Edge). Experience with Product Environmental Compliance (PEC) documentation. Our Culture & Commitment to You At Emerson, we prioritize a workplace where every employee is valued, respected, and empowered to grow. We foster an environment that encourages innovation, collaboration, and diverse perspectives—because we know that great ideas come from great teams. Our commitment to ongoing career development and growing an inclusive culture ensures you have the support to thrive. Whether through mentorship, training, or leadership opportunities, we invest in your success so you can make a lasting impact. We believe diverse teams, working together are key to driving growth and delivering business results. We recognize the importance of employee wellbeing. We prioritize providing competitive benefits plans, a variety of medical insurance plans, Employee Assistance Program, employee resource groups, recognition, and much more. Our culture offers flexible time off plans, including paid parental leave (maternal and paternal), vacation and holiday leave. Show more Show less

Role & responsibilities We are Hiring For "Medical Coders" Certification is Mandatory / Qualification: Any Degree CODERS : Minimum 1 year relevant experience is mandatory 1. IPDRG Coder : Noida / Hyd / Chennai / Mumbai || CTc up to 13 LPA || 2. Surgery Coder : Hyderabad / Chennai || CTc up to 10 lpa || 3. Denials : Chennai / Hyderabad|| CTc up to 10 lpa || 4. Radiology : Chennai / Trichy / bangalore || up to 48k Take home || 5.Anesthesia : Hyderabad || take home up to 48k || 6. ED Profee: Chennai / Bangalore || take home up to 48k || 7. ED Facility & Profee : Chennai || Upto 8lpa || QUALITY ANALYST: Min 4 years as a Coder and 1 year exp as QA on (Or) off paper 1. Surgery : Hyderabad/ Chennai / Bangalore || take home up to 60k || 2. EM IP : Chennai , Bangalore || take home up to 60k || 3. IP drg : Hyderabad || CTC up to 12lpa || 4. EM Op : Bangalore , chennai || take home up to 60k || 5. Anesthesia : Hyderabad || take home up to 60k || PROCESS COACH: Min 4 years as a Coder and 1 year exp as QA on (Or) off paper 1. SDS : Bangalore , Chennai || CTC Up to 9LPA || 2. EM : Bangalore , Chennai || CTC Up to 9LPA || TEAM LEAD: Min 6 years exp as coder with exp 1 year (on papers) team lead 1. SDS : Bangalore , Chennai || CTC Up to 12LPA || 2. Home Health : Bangalore || CTC Up to 12 LPA || 3. EM : Bangalore , Chennai || CTC Up to 12 LPA || Work from office / Relieving is mandatory Interested candidates can share your updated resume to HR Rama devi 7842224022 (Via What's app) Reference are highly appreciated Preferred candidate profile

At PwC, our people in business application consulting specialise in consulting services for a variety of business applications, helping clients optimise operational efficiency. These individuals analyse client needs, implement software solutions, and provide training and support for seamless integration and utilisation of business applications, enabling clients to achieve their strategic objectives. In SAP supply chain and operations at PwC, you will specialise in providing consulting services for SAP supply chain and operations applications. You will analyse client needs, implement software solutions, and offer training and support for seamless integration and utilisation of SAP supply chain and operations applications. Working in this area, you will enable clients to optimise their supply chain processes, improve operational efficiency, and achieve their strategic objectives. Focused on relationships, you are building meaningful client connections, and learning how to manage and inspire others. Navigating increasingly complex situations, you are growing your personal brand, deepening technical expertise and awareness of your strengths. You are expected to anticipate the needs of your teams and clients, and to deliver quality. Embracing increased ambiguity, you are comfortable when the path forward isn’t clear, you ask questions, and you use these moments as opportunities to grow. Skills Examples of the skills, knowledge, and experiences you need to lead and deliver value at this level include but are not limited to: Respond effectively to the diverse perspectives, needs, and feelings of others. Use a broad range of tools, methodologies and techniques to generate new ideas and solve problems. Use critical thinking to break down complex concepts. Understand the broader objectives of your project or role and how your work fits into the overall strategy. Develop a deeper understanding of the business context and how it is changing. Use reflection to develop self awareness, enhance strengths and address development areas. Interpret data to inform insights and recommendations. Uphold and reinforce professional and technical standards (e.g. refer to specific PwC tax and audit guidance), the Firm's code of conduct, and independence requirements. Job Summary - At PwC we relentlessly focus on working with our clients to bring the power of technology and humans together and create simple, yet powerful solutions. We imagine a day when our clients can simply focus on their business knowing that they have a trusted partner for their IT needs. Every day we are motivated and passionate about making our clients’ better. Within our Managed Services platform, PwC delivers integrated services and solutions that are grounded in deep industry experience and powered by the talent that you would expect from the PwC brand. The PwC Managed Services platform delivers scalable solutions that add greater value to our client’s enterprise through technology and human-enabled experiences. Our team of highly-skilled and trained global professionals, combined with the use of the latest advancements in technology and process, allows us to provide effective and efficient outcomes. With PwC’s Managed Services our client’s are able to focus on accelerating their priorities, including optimizing operations and accelerating outcomes. PwC brings a consultative first approach to operations, leveraging our deep industry insights combined with world class talent and assets to enable transformational journeys that drive sustained client outcomes. Our clients need flexible access to world class business and technology capabilities that keep pace with today’s dynamic business environment. Within our global, Managed Services platform, we provide Application Evolution Services (formerly Application Managed Services), where we focus more so on the evolution of our clients’ applications and cloud portfolio. Our focus is to empower our client’s to navigate and capture the value of their application portfolio while cost-effectively operating and protecting their solutions. We do this so that our clients can focus on what matters most to your business: accelerating growth that is dynamic, efficient and cost-effective. As a member of our Application Evolution Services (AES) team, we are looking for candidates who thrive working in a high-paced work environment capable of working on a mix of critical Application Evolution Service offerings and engagement including help desk support, enhancement and optimization work, as well as strategic roadmap and advisory level work. It will also be key to lend experience and effort in helping win and support customer engagements from not only a technical perspective, but also a relationship perspective. Minimum Degree Required (BQ) *: BE / B Tech / ME / M Tech / MBA / B.SC / B. Com / BBA Required Field(s) Of Study (BQ) Preferred Field(s) of Study: Minimum Year(s) of Experience (BQ) *: 6-10 years of experience Certification(s) Preferred Preferred Knowledge/Skills *: General Skill Set As a Senior Associate, you'll work as part of a team of problem solvers, helping to solve complex business issues from strategy to execution. PwC Professional skills and responsibilities for this management level include but are not limited to: Use feedback and reflection to develop self-awareness, personal strengths and address development areas. Proven track record as an SME in chosen domain. Ability to come up with Client POC/POV for integrating/increasing adoption of emerging Tech. like Blockchain, AI et al with the product platform they are associated with. Mentor Junior resources within the team, conduct KSS and lessons learnt. Flexible to work in stretch opportunities/assignments. Demonstrate critical thinking and the ability to bring order to unstructured problems. Ticket Quality and deliverables review. Status Reporting for the project. Adherence to SLAs, experience in incident management, change management and problem management. Review your work and that of others for quality, accuracy and relevance. Know how and when to use tools available for a given situation and can explain the reasons for this choice. Seek and embrace opportunities which give exposure to different situations, environments and perspectives. Use straightforward communication, in a structured way, when influencing and connecting with others. Able to read situations and modify behavior to build quality relationships. Uphold the firm's code of ethics and business conduct. Demonstrate leadership capabilities by working with clients directly and leading the engagement. Work in a team environment that includes client interactions, workstream management, and cross-team collaboration. Good Team player. Take up cross competency work and contribute to COE activities. Escalation/Risk management. Strong Knowledge In Understand client requirements, provide solutions, functional specifications and implement technical components accordingly. Possesses excellent experience in functional and technical requirements, study of business blue- prints, designing, development, fit-gaps, workshops, realization, testing, end-user training & support. Excellent Communication, analytical and Interpersonal skills as a Consultant and play a role of team lead. The successful candidate should be proficient in SAP EHS PS solution functionality, including specification database design (hierarchy, compositions, inheritance, value assignment), safety data sheet (SDS) authoring and distribution, label creation and generation (using SAP or other solutions), and hazardous materials classification and shipping (DG). Expertise in WWI template building and management, 3E content data loading and management (using OCC/Optimize Broker), and managing expert rules configuration (Expert). Familiarity with EHS PS Configurations, including Generation server (GenPC) and Expert servers. At least one end-to-end SAP EHS greenfield or brownfield implementation experiences, along with experience in rollouts and application maintenance/support projects. Troubleshoot and resolve issues related to EHS SAP configurations and custom development. Ensure that EHS solutions meet regulatory compliance and industry standards. Knowledge of integrating EHS with TMS (Dangerous Goods Management), EWM (Hazard Substance Management), and logistics (EHS outbound process). Provide support and training to end-users on SAP EHS functionality. Troubleshoot user issues and provide solutions to improve their SAP EHS experience. Excellent cross functional knowledge and integration skills with MM-FI and SD. Excellent verbal and written communication skills, in order to facilitate business/ technical discussions, document solutions and work well with people at all levels of the organization. Experience in Blue print, configuration and all phases of testing, documentation and production support. SAP EHS - Environmental, Human Compliance and IM Customizing of Inventory Management No. range for GR GI, as an Movement type. Experience on physical inventory Documents respective to Storage Location. Experiences in configuration of AAC Determination along with defining Valuation class, account cat. Reference, movement type, and account grouping of movement types. Customization of Logistics Invoice Verification document types, no. range for Logistic document and Evaluated receipt settlement (ERS). Experience on material pricing and tax on Purchase. Responsible for various phases of Testing: Testing strategy, Test scripts, End user testing, Test plans and End user authorizations acceptance. Must have design, configuration and support experience in WM/LE module: Inbound/outbound/manufacturing process with Warehouse, VAS, Picking, Packing, HUM, Cross docking, Yard management, Labor management, Physical inventory, Shipment, Internal Warehouse Processes and return process. Experienced in designing labels, Barcode Scanners, RF implementation and support. Detailed knowledge of systems and business processes within SAP Supply Chain and Logistics Execution modules (WM) and other SAP cross functional experience in MM, PP&SD. Must have Integration experience SAP with non-SAP external systems (Supplier collaboration, 3PL, etc.) /internal legacy systems. Integration experience with SAP 3PL preferred. Good experience in LOSC/POSC Preferred Skills SAP Certification on PM Module Used Solution Manager in the implementation Basic knowledge on ABAP ITIL 4 Foundation Certification Show more Show less

Openings of Surgery & ED Coders minimum 1 year of experience Certification not Mandatory WFO / Immediate JOINERS salary best in Industry Sujitha -- 7358399849 Varalakhsmi - 6385161155 Sindhuja - 7305158666 Nihila - 7305155582

Description As the Program Manager overseeing the Last Mile Payments & Services program within the AMZL organization, this position plays a pivotal role as the key liaison between Amazon Pay, VAS Category and the Last Mile. The 2 primary objective is to drive the (1) strategic vision of transitioning from cash to digital by promoting widespread adoption of DPOD (2) Driving Operational Efficiency for Value Added Services like Buyback Exchange program & Open Box Delivery program. Driving digital payments involves fostering growth in Amazon Pay users, increasing the utilization of Amazon Pay UPI (2P), encourageing the adoption of Pay wallet (1P), and reducing the Cost of Payments (COP) & Cost to serve. This role does collaboration with diverse set of external partners such as Ezetap (Now known as Razorpay) for enhancing payment success rate (PSR), and various customer and DA facing product/features development. Working closely with the A-pay marketing & business teams is imperative to implement targeted marketing campaigns effectively. This role also assumes a key position in delivering product launches and introducing key features by collaborating with the A-pay product team and NA tech team on multiple new product initiatives and roll-outs. Additionally, collaboration with the North Zone operations team is required to execute various campaigns aimed at achieving essential metrics such as Cashload, DPOD, 1P, 35P, SDS contacts, and NOC contacts for the zone. The Program Manager will play a crucial role in driving the SOP adherence for Buyback Exchange & Open Box Delivery program and improve customer experience. He/She will work very closely with operations team to identify blockers, come up with solutions and collaborate for roll-out of new initiatives. In this capacity, fostering collaboration with ACES is essential for Catalysts and training completion related to new product roll-outs and scorecard roll-outs. Engaging with Program teams is crucial for partner incentives and communication, while collaboration with the finance team is necessary for managing the FCF of the programs. Coordination with SDS and NOC is vital for managing contacts, and collaboration with SLP and other teams, such as the Chargeback teams, is essential for fraud and abuse prevention. Key job responsibilities The Program Manager in this position must possess the capability to spearhead groundbreaking initiatives for Amazon Pay & VAS Category team, taking the lead in the market with minimal guidance. They should demonstrate adeptness in independently managing evolving and conflicting priorities. The role entails conceptualizing new initiatives and product offerings, prioritizing both customer and operator experiences. The individual should possess the skill to exert influence without formal authority. Success in this role requires proficiency in Dive Deep, Ownership, Earn Trust, Customer Obsession, Invent and Simplify, and Deliver Results. Furthermore, the candidate should exhibit a visionary mindset, especially when considering projects with long-term, impactful outcomes. As the program owner, this role is responsible for overseeing the strategy and comprehensive implementation of OP2 charters and goals related to digital payments on delivery, Amazon Pay adoption, Roll-out fulfillment model for VAS, Defect Reduction in close collaboration with SLP / Ops. Successful end-to-end program management is crucial, demonstrating a thorough comprehension of business requirements and the ability to integrate them seamlessly with LM's robust operational capabilities. The role mandates a continuous exploration of innovative approaches to upscale pilots or intricate projects into larger initiatives. Additionally, it entails promptly addressing fraud-related cases, given their potential for substantial losses and regulatory repercussions if neglected. The individual must collaborate effectively with program management methodologies, utilizing escalation and risk mitigation strategies when necessary. Basic Qualifications 5+ years of working cross functionally with tech and non-tech teams experience 5+ years of program or project management experience 5+ years of delivering cross functional projects experience Experience defining program requirements and using data and metrics to determine improvements Preferred Qualifications 2+ years of driving process improvements experience Master's degree, or MBA in business, operations, human resources, adult education, organizational development, instructional design or related field Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner. Company - ATSPL - Delhi Job ID: A2980588 Show more Show less

Job Location : Kolkata Position : Company Secretary Experience : min 7 years post company secretary qualification Qualifications : Graduate with Company Secretary Industry : Joining : As soon as possible Skills : Good in english and presentable Skill : - - A strong understanding of corporate law, company regulations, and compliance requirements, - Knowledge in relevant legislation and regulations governing corporate governance, company formations, meetings, and filings. - Must have worked in a listed (BSE) Company - Should have knowledge on SEBI formalities and MCA formalities - Must be able to independently handle compliances related to Board meeting, AGMs etc. - Knowledge of SDS software - Good communication & strong analytical skill Job Description: Overall activities related to Company’s Act & Secretarial matters and various rules and regulation thereunder Conducting Board Meetings, General Meetings, Audit Committee Meeting, etc., as and when needed, , Prepare various draft agenda notes, Notice of Board Meeting, Committee Meeting & Annual General Meeting as per the Companies Act, Take minutes, draft resolutions, and lodge required forms and annual returns with appropriate authorities. File various statutory forms & returns, Maintain and record Statutory Registers as required under the Companies Act & Rules thereunder, Liaising with various statutory bodies like Registrar of Companies, other Government departments, etc. Pay dividends to shareholders and manage share option schemes opted by various shareholders. Formalities of SEBI & BSE / CSE as per Listing Agreement and upload all forms/details/xbrl at BSE & CSE including SDD Compliance Job Type: Full-time Pay: ₹1,000,000.00 - ₹1,500,000.00 per year Ability to commute/relocate: Manicktala, Kolkata, West Bengal: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Notice Period Current Salary Education: Bachelor's (Preferred) Experience: Listed company : 7 years (Preferred) Company Secretary: 7 years (Preferred) corporate law, company regulations, and compliance: 7 years (Preferred) worked in a listed Company: 7 years (Preferred) Company’s Act & Secretarial matters: 7 years (Preferred) SEBI formalities and MCA formalities: 7 years (Preferred) lodr: 7 years (Preferred) Language: English (Preferred) License/Certification: Company Secretary (Preferred) Location: Manicktala, Kolkata, West Bengal (Preferred) Work Location: In person

OPENINGS FOR GROUP COACH / QA / TEAM LEAD SPECIALTY IN ANESTHESIA OR SURGERY CODING OR E & M OBSERVATION CODING Location : Chennai / Hyderabad / Bangalore Required Candidate profile For more details contact: SUSHMI - 7397286767 DIVYA - 7358399847 Sindhuja - 7305158666 Rajitha - 9790878558 Varalakshmi - 6385161155

Description 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. Brief Job Overview This is a hands-on, non-supervisory, non-laboratory role in the India Biologics department. The incumbent work collaboratively in the reference standard/ARM development program within the Global Biologics department. The incumbent will participate in the development of replacement and new reference standards /ARM in support of USP’s mission and core business. The incumbent will also focus on supporting the suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports to assist in 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 timely 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) Has The Following Responsibilities Roles and Responsibilities Maintain smooth collaboration and works closely with key stakeholders across the globe to develop reference standards for biotechnology pharmaceutical products including proteins, peptides, heparins, antibiotics, and advanced therapies. Works to draft protocols, reports and address scientific and technical queries from internal and external stakeholders in timely manner pertaining to reference standards/ARMs Oversees and facilitates the development of standards and solutions to address analytical challenges associated with biological medicines. Supports day to day operations of the Stability (CSU) program covering the USP Biologics RS catalog inventory. Reviews RS testing history and drafts test protocols for collaborative studies and CSU studies and submits to labs based on designated testing requirements and schedules. Liaisons and Assists laboratories to ensure collaborative testing/CSU testing is completed accurately 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 current and historical Stability testing data assessment and prepare stability trend reports. Maintains and updates 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, Quality Assurance and Reference Standard Evaluation with 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 Reviews protocols and/or reports of other Scientists as assigned by manager. Who is USP Looking For? Preferred Qualifications 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: 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. Sr. Scientist I Ph.D. degree in Biochemistry, Analytical Chemistry or Biological Sciences . Minimum of 7 to 10 years of post-educational work experience in recombinant therapeutic proteins, peptides and carbohydrates. in Biochemistry, or Biological Sciences with minimum of 11 to 13 years of commensurate industrial experience. 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. Job Category Chemistry & Scientific Standards Job Type Full-Time Show more Show less

Position Title : Senior Scientific Officer/Scientific Officer- Quality Control- Electrophoresis and Chromatography lab Educational Qualification : M.Sc. / M.Tech -Biotechnology/ Microbiology Experience : 3 to 7 years Job Summary Senior Scientific Officer/Scientific Officer- Electrophoresis and Chromatography Lab (Quality Control) shall be responsible for ensuring the quality and efficacy of vaccine formulations at Vaccine Drug Substance Plant, Lalru (Punjab). This position will be responsible for overseeing the operation of HPLC, Weighing Balance operation, pH meter, Operation of densitometer, operation of tube heating block, testing of CRM-197 Protein by HPLC and SDS Page etc. Responsibilities: 1. Hands on Knowledge for operation of HPLC, Weighing Balance operation, pH meter, Operation of densitometer, operation of tube heating block, etc. 2. Hands on experience for testing of CRM-197 Protein by HPLC and SDS Page. 3. Hands on experience for testing of Free Carrier protein by HPLC on HiBTT, HiBTi conjugate and Pneumo conjugate 4. Hands on experience for testing of Molecular Size by HPLC on HiBTT, HiBTi conjugate and Pneumo conjugate 5. Ensure online documentation as per good documentation process. 6. Experience on Method validation for different products 7. Experience for evaluation of LOD/LOQ for rinse samples 8. Verification of Packing and consumables for Production department 9. Testing of Raw material and release. 10. Review of Analytical data’s tested for HPLC and Raw materials. 11. Proficient in analytical procedures and analytical method validations 12. Monitoring of ongoing testing activities on shop floor. 13. Issuance of Reference standards, Retention sample and Stability Sample. 14. Review of analytical data, capability to analyze the raw data of HPLC, GC, spectrophotometer etc JOB DESCRIPTION Name of Dept. Quality Control – Electrophoresis and Chromatography Lab. 15. Right allocation of manpower in shift working and monitoring of assigned task with optimum output. 16. Ensure Quality and quantity of consumables, Solutions with adequate usage & timely delivery to different manufacturing processes. 17. Right & Timely Documentation including SOPs, Change Controls, Deviations, Incidents, CAPA, Risk Assessments, in preview of PQS in view to regulatory guidelines & expectations. 18. Ensure zero non- compliance & zero data integrity in documentation. 19. Ensure regular maintenance of all equipment`s of production by engineering to achieve zero-breakdown. 20. Coordination with intra departmental activities in compliance to support/execution. Competencies Required: 1. Effective Communicator. 2. Motivate Team and Enable High Performance. 3. Effective Performance Reviews of the Team and their Training. 4. Must understand the team needs at the time testing, sample preparation 5. Must understand Sterile Operations, Scientific practices, analytical techniques & process criticalities of Vaccine manufacturing. 6. Analytical approach – Good in trend analysis, data evaluation & process calculations. 7. Adequate, Timely & Quality deliverance/ Output within stipulated timeframe. 8. Thorough understanding of PQS & its compliances with risk based approach. Show more Show less

Education: Bcom or Equivalent Experience : 2-3 Years Job Role : Proposal for SDS support ( Warranty, AMC, out of warranty) and co-ordinate with technical and commercial team RMA co-ordination closely working with internal sourcing, vendor and customer CHA Co-ordinate to collect customer feedback across all verticals and periodic reporting Mandatory Skills: Preparing Budget & Proposal, experience in handling Import and CHA co-ordination Desired Skills: Customer support co-ordination Soft Skills: Positive attitude towards work (Dynamic) Handling Multiple activities ( commercial, RMA, Supports) Ensure timely reporting and updates to stakeholders Close cooperation with other team members, Internal departments and vendors/customers Proficient in English and able to report, Analysis trends and presentation to team/Customer Show more Show less

Job Location : Kolkata Position : Company Secretary Experience : min 7 years post company secretary qualification Qualifications : Graduate with Company Secretary Industry : Joining : As soon as possible Skills : Good in english and presentable Skill : - - A strong understanding of corporate law, company regulations, and compliance requirements, - Knowledge in relevant legislation and regulations governing corporate governance, company formations, meetings, and filings. - Must have worked in a listed (BSE) Company - Should have knowledge on SEBI formalities and MCA formalities - Must be able to independently handle compliances related to Board meeting, AGMs etc. - Knowledge of SDS software - Good communication & strong analytical skill Job Description: Overall activities related to Company’s Act & Secretarial matters and various rules and regulation thereunder Conducting Board Meetings, General Meetings, Audit Committee Meeting, etc., as and when needed, , Prepare various draft agenda notes, Notice of Board Meeting, Committee Meeting & Annual General Meeting as per the Companies Act, Take minutes, draft resolutions, and lodge required forms and annual returns with appropriate authorities. File various statutory forms & returns, Maintain and record Statutory Registers as required under the Companies Act & Rules thereunder, Liaising with various statutory bodies like Registrar of Companies, other Government departments, etc. Pay dividends to shareholders and manage share option schemes opted by various shareholders. Formalities of SEBI & BSE / CSE as per Listing Agreement and upload all forms/details/xbrl at BSE & CSE including SDD Compliance Job Type: Full-time Pay: ₹1,000,000.00 - ₹1,500,000.00 per year Ability to commute/relocate: Manicktala, Kolkata, West Bengal: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Notice Period Current Salary Education: Bachelor's (Preferred) Experience: Listed company : 7 years (Preferred) Company Secretary: 7 years (Preferred) corporate law, company regulations, and compliance: 7 years (Preferred) worked in a listed Company: 7 years (Preferred) Company’s Act & Secretarial matters: 7 years (Preferred) SEBI formalities and MCA formalities: 7 years (Preferred) lodr: 7 years (Preferred) Language: English (Preferred) License/Certification: Company Secretary (Preferred) Location: Manicktala, Kolkata, West Bengal (Preferred) Work Location: In person

Greetings from Sagility !! Immediate for Auditor-Surgery coder(CPC Certified) Experience - 4+yrs Must have worked in Specializations like E\m IP&OP, Minor Surgery, SDS, General Surgery Must be CPC/ CCS Certified Must have a active certification (CPC/ CCS) Working Hours/ Days : 9 Hours / 5 Days a Week Shift : U.S Shift (4.30PM 1.30AM) Job Location : Bangalore Transportation will be provided Interested Candidates can share your CV - anitha.c@sagilityhealth.com.

SDS/2 Detailer Position Title: Steel Structure SDS/2 Detailer Position Overview : Having good experience in industrial project detailing using SDS/2 software with a good communication and coordination skill having minimum experience of 5 Years of experience. Position Duties : -Extracting information from structure and architecture drawing for model creation -Making complex 3D model with a good analyzation of fabrication and erection issue -Preparing 2D drawings& Erection drawings based on shop/ Field requirements -Flexibility to work different client standard based on requirement -Having knowledge of required settings on SDS/2 software. -Having knowledge of making different kind of user defined connection as per job requirements. -Specific communication skill to coordinate with external customer -Checking ability of final product produced by team Position Requirement : -Diploma or Degree in Civil/ Mechanical Engineering - Minimum of 5 years of experience in SDS/2 software -Ability to work in team environment -Ability to travel abroad as and when required

We are currently seeking an Assistant Manager ED/EM Medical Coding at Vee Healthtek. Job Description: - Must have over 8 years of experience in Medical Coding - Specialization in ED/EM Medical Coding - Experience of 8+ years on ED/EM - Designation: Assistant Manager - Location: Bangalore (Work from office) Candidates must have experience in team handling, with a minimum of 3 years in team management, excellent communication skills, and client management abilities. Interested candidates are encouraged to contact us immediately at 9443238706 (also available on Whatsapp) or send your profile to ramesh.m@veehealthtek.com. Best Regards, Ramesh HRD Vee Healthtek

Regulatory Compliance and Documentation Management: Maintain accurate knowledge of local regulatory requirements and ensure product compliance with national and/or international regulations. Develop and finalize product labels in alignment with country-specific requirements and oversee approval and production processes for India manufacturing. Create and maintain primary standard documents (including product specification, SDS, label, etc.) Support on BOM, variant and sample code creation. Regulatory Registrations, Stakeholder Liaison and Communication: Assist in preparing documents for product registrations dossier, imports and exports and custom clearance. Support the preparation of bi-annual reports such as heavy metal analyses for submission to FSSAI. Assist Manage FSSAI Manufacturing, Import, and Export Licenses for KFT products. Act as a liaison with regulatory officials, internally and externally, to ensure smooth information exchange in India. Support customer questionnaires, vendor registrations, and other regulatory or compliance tasks as needed. Audit and Training Support: Participate/support in internal audits and certifications renewal (E.g.: FOSTAC, HALAL, FSSC22000, etc.) Project Involvement: Support on PTP, PRI, PIP, or any other initiatives under the guidance of the Manager. Conduct research to support regulatory strategies and processes.

Job Title: Senior Node. js and Python Azure developer ( AWS to Azure Migration expert) Experience : 7-10 Yrs. Primary Skills: Python, PySpark - Python API Hands-on experience with Azure, Serverless (Azure Functions) AWS to Azure Cloud Migration (Preferred) Nice to have: Experience in Databricks , ADF mapping dataflow and Synapse Spark Scope of Work: Hand-on experience in migration of Python application from AWS to Azure environment Experience in PySpark - Python API Experience in Databricks , ADF mapping dataflow and Synapse Spark 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. 8+ years of experience in application development with Python Experience in Unit testing, application testing support and troubleshooting on Azure. Experience in application deployment scripts/pipelines, App service, 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 PaaS or Serverless. Tech stack details: Confluent Kafka AWS S3 Sync connector Azure Blob Storage AWS lambda to Azure Functions (Serverless) - Python S3 to Azure Blob Storage AWS to Azure SDK Conversion (Must Have)

Qualifications Educational qualification: B.E./B.TECH/M.E./M.Tech ECE, EEE, CSE Experience : 3-6 years Mandatory/requires Skills : Thorough Embedded C programming knowledge & experience (especially pointers, structures, linked lists etc.,) & Assembly programming knowledge Hands On Experience for Device Driver development with any of standard protocols such as SPI, UART, USB etc., Thorough RTOS knowledge and experience (Mutex, spinlocks, Queues, Signaling, Events, Deferred function calls & Callbacks, Multi-thread & Multi-process environments, Concurrency Scenarios etc.,), Linux Knowledge, Kernel & User Space knowledge Thorough experience of Operating systems, Microprocessor / computer architecture. Strong analytical and debugging skills Hardware and architectural knowledge / experience (Processor Architecture, Cache, interrupts, Memory barriers, Strong ordering etc.,) Emulator, simulator environment & JTAG debugging knowledge / experience Nice to Have - Hands On Experience or knowledge for Inter Processor Communication Protocol, Debug Logging framework, Heap Management & Timer implementations

Greetings from Coronis Ajuba (Formerly known as MiraMed Ajuba) We are looking for Experienced certified Surgery & IPDRG Auditors medical coders to join us. Interested candidates please call us @ 91+ 6385272597 or mail to manojprassana.dillibabu@coronishealth.com to book interview slot. SURGERY Coders ( 3 to 8 yrs ) * Certified coders only * Experience : 2+ yrs of experience in SDS is must * Location : Hyderabad / Chennai * Work from Office * Competitive Salary with Food and other Benefits. * Immediate Joiners preferred IPDRG Coders & Auditors ( 3 to 12 yrs ) * Experience : 1 to 10 years * Only for Certified coders * Location : Hyderabad / Chennai * Work from Office * Competitive Salary with Food and other Benefits. * Immediate Joiners preferred Attractive Salary for immediate joiners. Grab the opportunity and refer your friends Interested Candidates send you resume to the below WhatsApp Number or Reach me out on 6385272597 Regards, Manoj - 6385272597 Human Resources Coronis Ajuba

Hi All interview Started For CODERS & QA and offer Release also Started Coding Denials (Multispecialty) - 1 year Above To JOIN WATSAPP GROUP PING TO 9344964267 TO KNOW MORE Updates Location - Chennai only any one willing to relocate to Chennai also can apply ONLY WORK FROM OFFICE Certified Must NOTICE Period Acceptable Designation - Medical Coder / QA / QC Shift: Day shift Send Updated Resume , Recent Photo with the Mentioned Details Your Interview Will Be Scheduled Name - Contact Number - Current Company - Experience - Certification - Take home salary - Expected salary - Certification Number - NOTICE PERIOD - Active Bond - Email ID - To JOIN WATSAPP GROUP PING TO 9344964267 Kindly share this to all friends who in need of jobs in Coding

Company: MedMetrix Job Title: EM IP & OP / IPDRG(4 yrs) / SDS / IVR Interview Mode: Walk-In Minimum Exp : 1.5 years Requirements: Degree in Healthcare or related field. Experience with medical coding and data management. Proficiency in Excel and healthcare systems. Address: :7th Floor , Millenia Business Park II, 4A Campus,143 , Dr. M.G.R. Road, Kandanchavadi, Perungudi,Chennai, Tamil Nadu 600096, India Contact: Ranjitha (HR) - 8807618852