Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us. Your Role: SDS Author is responsible for ensuring that the SDS is compliant with all applicable laws and regulations, as well as being accurate and up to date across the globe. He/she must accurately interpret and convey the information contained in the SDS and ensure that all relevant information is included. must be able to communicate effectively with suppliers, customers, and other external stakeholders. He/she must also have a good understanding of the company’s product line and the hazards associated with each product. Analyst must be able to work independently and be able to work collaboratively with other members of the team. He/she must be proactive in taking up decisions and making strategic moves. Who You Are Post graduate degree in Chemistry/Organic chemistry/Biotechnology. 2 to 6 years’ experience in relevant life science Field. (Preferably experience with GHS, CLP knowledge) Knowledge in Chemistry subject, in-depth understanding of Functional group, structures etc. Should judge the hazards based on structures and functional group. Ability to do similarity search and evaluate data from similar substance SAP user knowledge: (Limited proficiency expected). Navigation of different screens/transactions. Ability to create specification and search for proper data in SAP system Global Chemical Regulatory knowledge: Awareness about SDS and Hazards. Knowledge about Chemical Regulations and know how to classify. e.g., GHS, CLP etc. Know about digital tools and advanced excel. Key skills and abilities on process improvements, Kaizen ideas. Ability to lead a projects. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! Show more Show less

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 data and analytics at PwC, you will specialise in providing consulting services for data and analytics solutions using SAP technologies. You will analyse client requirements, design and implement data management and analytics solutions, and provide training and support for effective utilisation of SAP data and analytics tools. Working in this area, you will work closely with clients to understand their data needs, develop data models, perform data analysis, and create visualisations and reports to support data-driven decision-making, helping them optimise their data management processes, enhance data quality, and derive valuable insights from their data to achieve their strategic objectives. Having good experience in Data Migration as well as SAP BODS as added advantage. Working with SAP functional and technical consultants analysing data migration requirements and the make-up of legacy data. Designing appropriate data migration solutions including, where required, transformation routines. SAP ECC Data source analysis and profiling to understand whether data will conform to target S/4 system and has data quality issues Building, testing, executing and managing data migrations utilising tools such as SAP SDS LSMW or SAP Data Services solutions. Delivery experience of SAP Migration Cockpit essential- LTMC and customisation of LTMOM to add new fields where required. Preload and post load validation of migration results, handle dropouts and advise on data cleansing requirements. Perform migration dress rehearsals, migration cutover tasks and post go-live support. Providing advisory services to the business to understand their data management issues and advising on appropriate data management strategies and techniques. Extensive experience of data management and migration activities in a SAP environment. Strong experience in the design and implementation of SAP's ETL solutions such as SAP Data Services and SAP LSMW, and additionally integration technologies such as IDOCs and BAPIs. Implement Data Migration framework as per data migration architecture using SAP Data Services and Information Steward . Create Technical Specification documents by utilizing Data migration experience and computer program knowledge which will be used in creation of Data services Jobs. Support Data Cleansing activities as required, using Information Steward, Excel, Data Services and SQL tools and also support data validation exercises of data through SIT, UAT and PROD cut-over. Experience of Snaplogic for migrating data from source and loading into S/4 HANA is an added advantage Positional Requirement Strong Technical Knowledge on Data Migration and Prior Project Lead experience Experience 5 to 9 years of experience Preferred Skills Snaplogic, SAP BODS, LTMC, Information Steward Preferred Knowledge Technical Knowledge on Snaplogic Additional Job Description Additional Job Description Professional & Educational Background B.TECH, B.E./Any Graduate Show more Show less

Description At Amazon, our mission is to be the most customer-centric company on earth. To achieve this, we need exceptionally talented, driven individuals. As one of the most recognizable brands globally, Amazon delivers millions of products annually to our loyal customers. The Shipping & Delivery Support (SDS) Learning Organization within the Ops Empowerment (OE) team is dedicated to creating, maintaining, and delivering training for SDS contact center associates across multiple countries and lines of business. We are currently seeking a Training Manager to join our India team. This role is ideal for professionals who thrive in dynamic, fast-paced environments, with a strong background in contact centers, training, and team management. As the Training Manager, you will be responsible for coordinating and managing all training initiatives across various workflows, while leading and developing a team of trainers. You will collaborate closely with Operations Managers, global Training Managers, regional Managers, and Subject Matter Experts (SME) to ensure consistency and effectiveness in training delivery. We are seeking a team player who can not only lead their own team but also work closely with stakeholders to prioritize and deploy training programs that meet customer needs. If you’re passionate about learning and love a challenge, we want you on our team! Key job responsibilities The role involves managing the development and delivery of complex, medium to large-scale training programs, often at a site or regional level supporting the IN market. This includes expert-level training facilitation, mentoring training specialists, and setting standards for training delivery. The role also requires ownership of stakeholder communication, gathering feedback, and implementing metrics to measure training success. As a subject matter expert (SME) in training facilitation, you will proactively identify risks, resolves complex issues, and drives operational efficiencies. The role includes identifying and sharing best practices, scoping out new metrics and tools, and making data-driven decisions while considering diverse opinions. The individual is responsible for increasing efficiency, raising productivity, and reducing costs at a site or regional level. This includes conducting root cause analysis, identifying program gaps, and driving continuous improvement with stakeholders. Managers also serve as an escalation point for site-level decisions, partnering with leadership to address local and regional needs. Additionally, the role requires effective communication and deep understanding of metrics, analysis, and updates, often delivering detailed narratives to influence business direction. A day in the life On any given day, your responsibilities will include but are not limited to: Tracking, recording, and reporting training progress to stakeholders. Coaching and developing trainers to enhance their skills and effectiveness. Identifying and addressing knowledge gaps within the team. Collaborating with stakeholders to finalize training needs, durations, and schedules. Participating in global projects and attending relevant meetings. Ensuring that all training processes are consistently followed and adhered to. Basic Qualifications Completed a bachelor's degree from an accredited university. 3 to 5 years of experience managing a team, supporting their success and career growth Fluent in both English and Hindi languages, written and spoken Ability to collaborate effectively with local stakeholders, SMEs, front-line managers, and employees. Has experience in doing root cause analysis (RCA), and analyze customer needs Has proficiency in understanding and reading data Proficient in Microsoft Office tools, including Word, Excel, Outlook, and PowerPoint. Blue Badge Employee with at least 2 years tenure or more (*for Internal candidates) Preferred Qualifications 3+ years of experience in training delivery within a corporate environment, with a proven track record in planning and implementing effective training programs. Learning/training certification in eLearning, and industry certifications in instructional design, curriculum development, performance improvement, project management, or related areas (e.g., CPLP, CPT, PMP). Strong knowledge of adult learning theory, training evaluations, and best practices. Hands-on experience in training facilitation in both classroom and virtual settings. Experience with Learning Management Systems (LMS) for tracking and measuring training results and learning effectiveness. Demonstrated proficiency in eLearning development tools like Captivate, Articulate Studio/Storyline, Camtasia, Adobe Photoshop/Illustrator, or Flash. Familiarity with Amazon collaboration tools such as Amazon Workdocs, Quip, Asana, and a solid understanding of KNet/Amazon Learn. Experience with Amazon AI tools like Cedric, Partyrock, etc. Prior experience in a training and development role, specifically within customer service. Proven ability to present to an audience and convey complex information in an engaging and understandable manner. Experience developing training materials, job aids, and online tutorials, with a solid understanding of adult learning and training practices. Demonstrated ability to work effectively in a cross-functional, global environment, showing cultural sensitivity and earning trust from stakeholders. Excellent written and verbal English and Hindi communication skills. Experience in applications such as QuickSight, PowerBI, Tableau, and able to make sense of the data provided by the systems 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 - ADCI HYD 20 SEZ - H94 Job ID: A2995066 Show more Show less

Role- SDS Supervisor Job Purpose The Supervisor, Coding is responsible for the supervision activities and operations of the overall functions of the Coding department and staff. Duties and Responsibilities Organizes, directs, and monitors daily activities of Coding Associates as it relates to coding edits and denials Distributes workload to team; monitors and reviews performance Monitors and analyzes productivity of the coding department employees, completes employee evaluations Fields questions from Coding Associates and Auditors as well as clients Establishes procedures, prepares and coordinates schedules, and expedites workflow Prepares reports and correspondence as needed Compiles status and work-volume reports for management Interviews, trains, motivates, and rewards Coding department staff Manages disciplinary personnel issues and escalates accordingly Assists with the implementation of policies and procedures necessary to comply with federal, state, and third-party regulations which govern billing and collection activities for physician services Performs Coding Department duties as needed Performs other related duties as assigned by management Use, protect and disclose patients protected health information (PHI) only in accordance with Health Insurance Portability and Accountability Act (HIPAA) standards Qualifications Bachelors degree equivalent combination of education and experience CPC or CCS Coding certification required from AHIMA or AAPC 1-3 years’ experience as a Supervisor Possess thorough knowledge of multispecialty coding, including CPT, ICD-10 and HCPCs codes Related training/experience (preferably within the past five years) Knowledge of Medicare, Medicaid and Managed Care guidelines Proficiency in the use of Excel Spreadsheets, PowerPoint, and various software programs Excellent interpersonal and organizational skills Strong leadership, independent thinking and decision-making skills Strong organizational, problem-solving, and analytical skills Excellent oral and written communication skills Ability to communicate with all members of the health care team Ability to prioritize assignments

About Valdera: At Valdera, we empower innovators to turn ideas into reality by transforming how manufacturers source materials. We make it effortless for companies to find the best materials and suppliers for their needs, enabling them to build high-quality products at scale and deliver them to millions of consumers worldwide. We are a team of ambitious, results-driven individuals with a proven track record of working with Fortune 500 industrial manufacturers, beauty brands, and chemical companies. We are a fast-growing company that hires talented, hardworking people who excel in high-performance environments and want to grow their careers quickly. Our culture is built for exceptional individuals to take on meaningful challenges, collaborate with the top minds in our industry, and see the direct impact of their work. If you’re looking for a fast-paced environment where your ideas will drive real change, Valdera is the place for you. Join us, and let’s shape the future of manufacturing together. Role Description: Valdera is seeking a Chemicals Market Research Analyst to strengthen our supplier intelligence and data capabilities across a broad range of commodity and specialty chemicals. In this role, you’ll be instrumental in enhancing and expanding our supplier data that powers Valdera’s procurement platform—delivering accurate, timely, and actionable insights for buyers and internal stakeholders. You will lead efforts to identify and validate suppliers, assess chemical value chains, and track market dynamics. Your work will ensure that Valdera maintains a robust understanding of the global chemical supply landscape. Role Responsibilities: Conduct supply market assessments for commodity and specialty chemicals Identification of suppliers for specific materials across of wide range of chemical value chains Identifies and monitors key trends (e.g., price spikes, force major, etc.) for selected chemical value chains Conduct primary and secondary research to validate supplier product information, grade availability, capacity, etc. Identification and validation of key supplier contacts across selected organizations Guide data entry specialists to document relevant product and contact information from suppliers Collaborates with data engineering team to validate data and build out database Experience & Qualifications: 3+ years of experience in industry research across commodity and specialty chemicals sectors Prior experience in top-tier chemicals market research environments (e.g., management consulting research teams or leading industry information service providers) Demonstrated ability to conduct supply market assessments and identify suppliers for specific chemicals / raw materials Extensive knowledge of chemicals / raw materials and relevant technical expertise in reviewing RFQs (TDS, SDS, COA, etc.) Deep understanding of chemical industry including key players, industry trends, manufacturing technologies Extensive experience in applied research including identifying and collecting relevant data source through primary and secondary research Salary Range: Salary ranges are determined by multiple factors, including the labor market, market compensation bands, internal parity, and budget considerations. The final offer will be based on the candidate’s individual skills, qualifications, location, and experience relative to the requirements of the role. Benefits: Valdera offers generous benefits to employees. You will be provided a more detailed breakdown of your options prior to joining Valdera. Equal Opportunity Employer Statement: Valdera is an equal-opportunity employer committed to building a diverse and inclusive team. We welcome applicants of all backgrounds and celebrate a culture that values varied perspectives, skills, and experiences. We are dedicated to maintaining a workplace free from discrimination, where everyone feels valued, respected, and empowered to contribute. Show more Show less

Role & responsibilities Junior detailer Prepare shop drawings using SDS software. Create fabrication drawings for steel structures. Ensure accuracy in drafting and detailing of steel components. Collaborate with engineers to resolve design issues. Model steel structures using CAD software. Preferred candidate profile 1.Bachelor's degree in civil or mechanical. 2.Eligible criteria: 2023/2024 or 2025(No arrears) 3.Must have knowledge in engineering drawings. 4.CGPA:7 and above Desired Candidate Profile 0-3 years of experience in civil engineering or related field (structural detailing). Strong understanding of structural fabrication techniques and materials. Diploma or B.Tech/B.E. degree in Civil or Mechanical Engineering from a recognized institution.

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, color religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description We are seeking an associate for the Quality control -Analytical team responsible for conducting analysis of Biosimilar products ( drug substance , drug products and their in-process samples and stability samples). The role involves ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety. " Roles & Responsibilities To perform analysis in Quality control analytical laboratory for the Biosimilar /Biologics Products as per the planning allotted by Team lead To perform chromatography techniques like RP-HPLC, Glycan, SEC, IEX, pep map for Biosimilar Molecules Having 2 to 6 years of experience Method Validations on RP-HPLC, Glycan, SEC, IEX, pep map To Perform Biochemical, Physico chemical and chromatographic analysis Adhering to GMP practices Adhering to Good documentation practices Adhering to Good Analytical Practices Adhering to Regulatory Requirements including Internal or External audits, Audit readiness and Query response drafting. Adhering to compliance of systems in Quality Control, by working with relevant stake holders To adhere and follow the safety practices and procedures. To adhere to various cGMP procedures and internal SOPs Qualifications Educational qualification: A Masters' degree in Biotechnology/ BE Biotechnology/B Tech Biotechnology or in Biochemistry domain. Minimum work experience: 2 to 6 years of experience in QC analytical testing in Biosimilar products Skills & attributes: Technical Skills Proficient in handling SEC/RP/IEX/Peptide Mapping/Glycan analysis of Biosimilar Products Proficient in handling of Gel electrophoresis/CE/HCP/HCD analysis of Biosimilar products Knowledgeable about cGMP, SOPs, and STPs, ensuring accurate documentation and adherence to specifications. Adheres to safety precautions and procedures during analysis, emphasizing the importance of lab safety, JSA (Job Safety Analysis), and proper use of PPE (Personal Protective Equipment). Expertise in handling and upkeep of the chemical and solvent store, including the preparation and maintenance of volumetric solutions and reagents. Method Validations on HCP/HCD/CZE/SDS PAGE Behavioural Skills Keen attention to detail in analysis and documentation, ensuring accuracy in all tasks. Effective communication and collaboration skills for communicating with the Group Leader, reporting discrepancies, incidents, and providing timely updates. Takes initiative in ensuring the proper use and care of instruments, timely destruction of samples, and other assigned responsibilities. Demonstrates problem-solving skills in addressing discrepancies, incidents, and ensuring smooth laboratory operations. Upholds ethical standards, compliance with SOPs, and follows regulatory requirements in all activities. Additional Information Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions... For more details, please visit our career website at https://careers.drreddys.com/#!/ Show more Show less

Role & responsibilities 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

Job Title: Product Stewardship Specialist II - Regulatory Services Summary: This position is responsible for Product Stewardship Regulatory services around dossier preparation and submission (e.g. EU-REACH, UK-REACH, KKDIK, etc.). Establish and maintain processes (e.g. e-SDS, C&L notifications, Trade secret Notifications). Effective coordination between internal and external functions and stakeholders. The role covers the activity for products from all Business Segments, ensuring continuity and growth of these businesses through compliance with regulations. Works directly with all levels within Momentive businesses and direct resources, with appropriate expertise in supporting Substance/product registration strategy and execution for existing products, new product introduction and development, product portfolio and strategic risk assessments. Responsibilities Include: Responsibility / Project Management Responsible to coordinate and lead defined scope registration projects within Product Stewardship. Support development of SOPs and work instructions in the dossier creation domain. Responsible for data management and identification and resolution of data inconsistencies and gaps within core function. Responsible to identify and protect confidential product stewardship information. Execution Execute focused registration projects independently. Participate in multiple activities without compromising delivery. Provide accurate, consistent, and on-time responses to internal and external customers. Independently research and collect information in support of compliance related programs. Collaboration & Communication Share information cross-functionally and ensure appropriate experts and stakeholders are included. Analyze the stakeholders and adapt the communication to the audience. Routinely share information and learnings within PS Team and in meetings. Execute or drive multiple cross-functional and PS Team regulatory needs and activities in Sprint model. Regulatory Skills Responsible for providing comprehensive information on regulatory knowledge and industry expertise (e.g. REACH, UK-REACH, KKDIK). Support with e-SDS authoring, C&L and Trade secret Notifications Drives necessary actions related to changing chemical regulations within Product Stewardship. Technical Skills Responsible for applying concepts and principles with proactive use of existing or new technology. Working experience with IUCLID, Chesar, REACH IT, SAP EHS. Identify opportunities for new templates and process improvements & learn about potential solutions. Leverages knowledge and mentor others on SME topics within the PS organization. Process Skills Proactively compile information to demonstrate and describe the benefit to the organization on defined process improvement projects. Full understanding on the processes required to submit, maintain and upgrade dossiers under REACH(-like) schemes for Lead dossiers, joint submissions, co-registrations and OR services. Lead small process improvement projects. Knowledge Conduct training of silicone chemistry in specialized areas as well as industry practices, techniques, and standards. Work independently with IUCLID and relevant business tools to provide basic training to others. Qualifications: The following are required for the role Minimum Qualifications: Technical degree in Engineering, Pharmacy, Chemistry, Biology, Life Science, Environmental Science, Industrial Hygiene, Safety Engineering, Public Health or equivalent Minimum 8 to 10 years, relevant experience in the chemical or related industry in the area of Product Stewardship and Regulatory Compliance or other applicable experience. Business Acumen, ability to inform business and influence decision making. Hands on experience on IUCLID, REACH IT. Basic chemistry skills related to product chemistry. Basic Toxicology skills Ability to work cross-functionally and proactively establish connections. Excellent interpersonal skills. Able to work, lead, and manage across functions in a global organization with matrix reporting structure. Strong working knowledge of product regulatory legislation and regulation in the regions/countries within job scope. Flexibility to focus on chemistry-related topics, customer support and fulfilling legal requirements. Proven organizational and project management skills. Able to manage multiple priorities simultaneously. Excellent English verbal and written communication and presentation skills. Computer literate in standard office systems. Available for early morning or late evening global calls as needed. Able to travel, including internationally, as needed and work in a chemical plant environment. Preferred Qualifications: Experience in Silicones industry and/or with highly regulated end use markets in which Momentive operates (personal care, agriculture, healthcare, food contact, etc.) Experience working directly with internal and external customers, understanding, and showing a high level of commitment and response to their needs. Hands on experience with Chesar Six Sigma Greenbelt SAP EHS experience. Project Management skills. Product Line Knowledge. What We Offer: At Momentive, we value your well-being and offer competitive total rewards and development programs. Our inclusive culture fosters a strong sense of belonging and provides diverse career opportunities to help you unleash your full potential. Together, through innovative problem-solving and collaboration, we strive to create sustainable solutions that make a meaningful impact. Join our Momentive team to open a bright future. #BePartoftheSolution About Us: Momentive is a premier global advanced materials company with a cutting-edge focus on silicones and specialty products. We deliver solutions designed to help propel our customer s products forward products that have a profound impact on all aspects of life, around the clock and from living rooms to outer space. With every innovation, Momentive creates a more sustainable future. Our vast product portfolio is made up of advanced silicones and specialty solutions that play an essential role in driving performance across a multitude of industries, including agriculture, automotive, aerospace, electronics, energy, healthcare, personal care, consumer products, building and construction, and more. Momentive believes a diverse workforce empowers our people, strengthens our business, and contributes to a sustainable world. We are proud to be an equal opportunity employer . Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any characteristic protected by law. To be considered for this position candidates are required to submit an application for employment and be of legal working age as defined by local law . An offer may be conditioned upon the successful completion of pre-employment conditions, as applicable, and subject to applicable laws and regulations . Note to third parties: Momentive is not seeking or accepting any unsolicited assistance from search and selection firms or employment agencies at this time.

Job Title: Advanced Product Steward - Regulatory Services Summary: This position is responsible for Product Stewardship Regulatory services around dossier preparation and submission (e.g. EU-REACH, UK-REACH, KKDIK, etc.). Establish and maintain processes (e.g., e-SDS, C&L notifications, Trade secret Notifications). Effective coordination between internal and external functions and stakeholders. The role covers the activity for products from all Business Segments, ensuring continuity and growth of these businesses through compliance with regulations. Works closely with the Business Teams with the focus on Substance/product registration strategy and execution to support new product development and product regulatory reviews. Proactively communicates legislative or regulatory changes that may impact the portfolio to the Business teams and helps to understand potential risks and opportunities. Provides training on dossier requirements and procedures as needed to the Business Teams and related Functions. Leads and/or participates in global Product Stewardship teams or projects. Responsibilities Include: Responsibility / Project Management Responsible for leading registration projects involving multifunctional stakeholders. Ensure on-time compliance activities. Responsible for reviewing new inquiries for impact assessment and identify the need for standardized responses. Lead documenting SOPs and work instructions in the dossier creation domain. Responsible for data management, elevating and resolving actions independently for data inconsistencies and gaps. Responsible to identify risks to loss of confidential product stewardship information. Educate others how to identify and protect confidential product stewardship information. Execution Lead Registration projects: collecting data from various team members, dossier completion, submission and follow up; ensure activities are executed. Manage multiple activities without compromising delivery. Responsible for researching and responding on time to technical inquiries within scope of expertise. Complete compliance tasks within deadlines and interim milestones. Collaboration & Communication Manage and facilitate stakeholder communications across functions and regions. Solve technical problems also by involving subject matter experts as needed. Lead the sharing of information and learnings within PS Team and in meetings. Coordinate multiple cross-functional and PS Team regulatory needs and activities in Sprint model. Regulatory Skills Responsible for providing comprehensive regulatory intelligence information and industry expertise on multiple topics (e.g. REACH, UK-REACH, KKDIK). Support in building processes for e-SDS authoring, C&L and Trade secret Notifications Responsible for interpreting, analyzing, and assessing the impact of new or changing regulations, and driving actions through multiple stakeholders to ensure compliance. Technical Skills Influence PS functional strategy from a technical perspective. Working experience with IUCLID, Chesar, REACH IT, SAP EHS. Ensure the company responds appropriately to upcoming regulations. Identify teaching opportunities / needs within and outside of the PS organization and endure follow-up action is taken to address these opportunities / needs. Process Skills Involved in the development of new concepts, techniques, and standards. Full understanding on the processes required to submit, maintain and upgrade dossiers under REACH(-like) schemes for Lead dossiers, joint submissions, co-registrations and OR services. Responsible to identify and lead productivity improvement projects. Knowledge Ensure to stay abreast on silicone chemistry, products, knowledge of end use applications and industry best practices. Train others in registration requirements and processes Basic Toxicology and Finance (LoA costing, Fees, PO s) Qualifications: The following are required for the role Minimum Qualifications: Technical degree in Engineering, Pharmacy, Chemistry, Biology, Life Science, Environmental Science, Industrial Hygiene, Safety Engineering, Public Health or equivalent Minimum 10 to 15 years, relevant experience in the chemical or related industry in the area of Product Stewardship and Regulatory Compliance or other applicable experience. Business Acumen, ability to inform business and influence decision making. Hands on experience on IUCLID, REACH IT, Chesar. Basic chemistry skills related to product chemistry. Basic Toxicology skills Ability to work cross-functionally and proactively establish connections. Excellent interpersonal skills. Able to work, lead, and manage across functions in a global organization with matrix reporting structure. Strong working knowledge of product regulatory legislation and regulation in the regions/countries within job scope. Flexibility to focus on chemistry-related topics, customer support and fulfilling legal requirements. Proven organizational and project management skills. Able to manage multiple priorities simultaneously. Excellent English verbal and written communication and presentation skills. Computer literate in standard office systems. Available for early morning or late evening global calls as needed. Able to travel, including internationally, as needed and work in a chemical plant environment. Preferred Qualifications: Experience in Silicones industry and/or with highly regulated end use markets in which Momentive operates (personal care, agriculture, healthcare, food contact, etc.) Experience working directly with internal and external customers, understanding, and showing a high level of commitment and response to their needs. Hands on experience with submitting DUINs, NRES Six Sigma Blackbelt or Greenbelt SAP EHS experience. Project Management skills. Product Line Knowledge. What We Offer: At Momentive, we value your well-being and offer competitive total rewards and development programs. Our inclusive culture fosters a strong sense of belonging and provides diverse career opportunities to help you unleash your full potential. Together, through innovative problem-solving and collaboration, we strive to create sustainable solutions that make a meaningful impact. Join our Momentive team to open a bright future. #BePartoftheSolution About Us: Momentive is a premier global advanced materials company with a cutting-edge focus on silicones and specialty products. We deliver solutions designed to help propel our customer s products forward products that have a profound impact on all aspects of life, around the clock and from living rooms to outer space. With every innovation, Momentive creates a more sustainable future. Our vast product portfolio is made up of advanced silicones and specialty solutions that play an essential role in driving performance across a multitude of industries, including agriculture, automotive, aerospace, electronics, energy, healthcare, personal care, consumer products, building and construction, and more. Momentive believes a diverse workforce empowers our people, strengthens our business, and contributes to a sustainable world. We are proud to be an equal opportunity employer . Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any characteristic protected by law. To be considered for this position candidates are required to submit an application for employment and be of legal working age as defined by local law . An offer may be conditioned upon the successful completion of pre-employment conditions, as applicable, and subject to applicable laws and regulations . Note to third parties: Momentive is not seeking or accepting any unsolicited assistance from search and selection firms or employment agencies at this time.

Hi All interview Started For CODERS & QA and offer Relese also Started QA/ QC EM OP - 3 year Above To JOIN WATSAPP GROUP PING TO 9655581000 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 Our supporting HR - Details Call Them Schedule Your Interviews Available Timing from 10.30 am to 6.30 pm Monday to Saturday Mohamed Nazarudeen 8903902178 Watsapp and call Sai Santosh 8925722891 watsapp and call Hashrithaa 9894654083 watsapp and call Karthick 9626985448 watsapp and call Ranjitha 8807618852 watsapp and call Surendearan 9600183612 WatsApp and call praveen 9655581000 WatsApp only 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 9655581000 Kinldy share this to all friends who in need of jobs in Coding

Hi All interview Started For CODERS & QA and offer Relese also Started Denial Coder QA/ QC - 3 year Above To JOIN WATSAPP GROUP PING TO 9655581000 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 Our supporting HR - Details Call Them Schedule Your Interviews Available Timing from 10.30 am to 6.30 pm Monday to Saturday Mohamed Nazarudeen 8903902178 Watsapp and call Sai Santosh 8925722891 watsapp and call Hashrithaa 9894654083 watsapp and call Karthick 9626985448 watsapp and call Ranjitha 8807618852 watsapp and call Surendearan 9600183612 WatsApp and call praveen 9655581000 WatsApp only 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 9655581000 Kinldy share this to all friends who in need of jobs in Coding

Hi All interview Started For CODERS & QA and offer Relese also Started QA / QC - ED Profee Facility + Ancillary - 3 year Above To JOIN WATSAPP GROUP PING TO 9655581000 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 Our supporting HR - Details Call Them Schedule Your Interviews Available Timing from 10.30 am to 6.30 pm Monday to Saturday Mohamed Nazarudeen 8903902178 Watsapp and call Sai Santosh 8925722891 watsapp and call Hashrithaa 9894654083 watsapp and call Karthick 9626985448 watsapp and call Ranjitha 8807618852 watsapp and call Surendearan 9600183612 WatsApp and call praveen 9655581000 WatsApp only 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 9655581000 Kinldy share this to all friends who in need of jobs in Coding

Hi All interview Started For CODERS & QA and offer Relese also Started Anesthesia -3 year Above QA / QC To JOIN WATSAPP GROUP PING TO 9655581000 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 Our supporting HR - Details Call Them Schedule Your Interviews Available Timing from 10.30 am to 6.30 pm Monday to Saturday Mohamed Nazarudeen 8903902178 Watsapp and call Sai Santosh 8925722891 watsapp and call Hashrithaa 9894654083 watsapp and call Karthick 9626985448 watsapp and call Ranjitha 8807618852 watsapp and call Surendearan 9600183612 WatsApp and call praveen 9655581000 WatsApp only 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 9655581000 Kinldy share this to all friends who in need of jobs in Coding

Hi All interview Started For CODERS & QA and offer Relese also Started QA/ QC - EM IP +OP + Hospitalist - 3 year Above To JOIN WATSAPP GROUP PING TO 9655581000 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 Our supporting HR - Details Call Them Schedule Your Interviews Available Timing from 10.30 am to 6.30 pm Monday to Saturday Mohamed Nazarudeen 8903902178 Watsapp and call Sai Santosh 8925722891 watsapp and call Hashrithaa 9894654083 watsapp and call Karthick 9626985448 watsapp and call Ranjitha 8807618852 watsapp and call Surendearan 9600183612 WatsApp and call praveen 9655581000 WatsApp only 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 9655581000 Kinldy share this to all friends who in need of jobs in Coding

Hi All interview Started For CODERS & QA and offer Relese also Started QA / QC Denials (Multispeciality) - 3 year Above To JOIN WATSAPP GROUP PING TO 9655581000 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 Our supporting HR - Details Call Them Schedule Your Interviews Available Timing from 10.30 am to 6.30 pm Monday to Saturday Mohamed Nazarudeen 8903902178 Watsapp and call Sai Santosh 8925722891 watsapp and call Hashrithaa 9894654083 watsapp and call Karthick 9626985448 watsapp and call Ranjitha 8807618852 watsapp and call Surendearan 9600183612 WatsApp and call praveen 9655581000 WatsApp only 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 9655581000 Kinldy share this to all friends who in need of jobs in Coding

Hi All interview Started For CODERS & QA and offer Relese also Started IPDRG QA - 3 Year Above To JOIN WATSAPP GROUP PING TO 9655581000 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 Our supporting HR - Details Call Them Schedule Your Interviews Available Timing from 10.30 am to 6.30 pm Monday to Saturday Mohamed Nazarudeen 8903902178 Watsapp and call Sai Santosh 8925722891 watsapp and call Hashrithaa 9894654083 watsapp and call Karthick 9626985448 watsapp and call Ranjitha 8807618852 watsapp and call Surendearan 9600183612 WatsApp and call praveen 9655581000 WatsApp only 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 9655581000 Kinldy share this to all friends who in need of jobs in Coding

Hey Family!!!! We have huge opportunity for our new MNC RCM client!!!! *Open Package - Medical coding* *Speciality: SDS - OP * *Designation* : 1. Senior Coder Work Location: *Bangalore & Chennai ,trivandram* *Speciality: IPDRG Coding* *Designation: Senior Coder* Work Location: *Coimbatore and Chennai* Eligibility: *Only Certified - Any certification like CPC ,CIC,CCS * Interview: Single Round Virtual Salary Grid: *Open* *Only Work from office* Notice period: *Immediate to 30days* Interested Candidates Reach Out to 7550062225 Thanks regards, Indhu Senior Lead HR Talent Acquisition Team 7550062225

Hiring For || Medical - Coders / QA / Process coach / TL || 12lpa || Certification is Mandatory / Qualification: Any Degree IPDRG - Service Delivery Head : Chennai 15+ Years Experience In IPDRG and Min 5 years into leadership (on papers) 2 Yrs Senior manager on paper is must ( Any certification ) Sigma Black Belt or PMP certification CODERS : 1. IPDRG Coder : Noida / Hyd / Chennai / Mumbai || CTc upto 13 LPA || 2. Surgery Coder : Hyderabad / Chennai / bangalore || CTc upto 10 lpa || 3. Denials : Chennai / Hyderabad || CTc upto 10 lpa || 4. Radiology : Chennai / bangalore || upto 48k Take home || 5. ENM : Chennai / bangalore || upto 48k Take home || 6. Anesthesia : Hyderabad || take home upto 48k || 7. ED Profee: Chennai / Bangalore || take home upto 48k || Experience : Minimum 1 year relevant experience is mandatory QUALITY ANALYST: 1. Surgery : Hyderabad/ Chennai / Bangalore || take home upto 60k || 2. Home Health : Chennai || CTC Upto 10 LPA || 3. IPdrg : Hyderabad || CTC upto 12lpa || 4. Denials : Hyderabad || CTc upto 9.5 lpa || 5. Radiology +IVr: Hyderabad || CTc upto 9.5 lpa || 6. Anesthesia : Hyderabad || take home upto 60k || 7. ENM : Chennai / bangalore || upto 60k Take home || Eligibility : Min 4 years as a Coder and 1 year exp as QA on (Or) off paper PROCESS COACH : 1. Surgery : Chennai / Bangalore || CTC Upto 9 LPA || 2. ENm : Chennai /Bangalore || CTC Upto 9 LPA || Eligibility : Min 4 years as a Coder and 1 year exp as QA on (Or) off paper TEAM LEAD: 1. SDS : Bangalore || CTC Upto 12 LPA || 2. Home Health : Bangalore || CTC Upto 12 LPA || 3. ENM : Bangalore || CTC Upto 12 LPA || Eligibility : Min 6 years exp as coder with exp 1 year (on papers) teamlead Work from office / Relieving is mandatory Interested candidates can share your updated resume to HR Mounika 9849854938 ( Via What's app ) Reference are highly appreciate

Dear Candidate, We are hiring a Prolog Developer to work on logic programming projects involving rule-based systems, AI inference engines, and natural language processing. Key Responsibilities: Design inference engines using Prolog or SWI-Prolog Build knowledge bases and implement predicate logic Integrate Prolog logic into modern applications via APIs or FFI Debug and optimize recursive query performance Collaborate on AI/NLP or knowledge graph projects Required Skills & Qualifications: Experience with Prolog , Horn clauses , and backtracking Familiarity with SWI-Prolog , Constraint Logic Programming (CLP) Background in AI , linguistics , or rule engines Bonus: Interfacing Prolog with Python , Java , or C Note: If interested, please share your updated resume and preferred time for a discussion. If shortlisted, our HR team will contact you. Kandi Srinivasa Reddy Delivery Manager Integra Technologies

Immediate Job Openings for Surgery Medical Coders @ Vee Healthtek Job Description: 1+ Years of Experience in Surgery Medical Coding. Specialty : Surgery Medical Coding Experience : 2 - 5 Years. Designation : Sr Coder/QA Certification: CPC/COC/CCS/CIC is Must Salary: 45K CTC Max Joining: Immediate Joiners only Location : Chennai/Bangalore/Hyderabad/Trichy/Salem/Pune - WFO Interested Candidate can Call Immediately to 9566406546(Available on Whatsapp) or forward your profile to kalaiyarasi.r@veehealthtek.com Regards, Kalaiyarasi Raja- HRD 9566406546 kalaiyarasi.r@veehealthtek.com Vee Healthtek

Hi All interview Started For CODERS & QA and offer Relese also Started IPDRG - 1 Year Above To JOIN WATSAPP GROUP PING TO 9655581000 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 Our supporting HR - Details Call Them Schedule Your Interviews Available Timing from 10.30 am to 6.30 pm Monday to Saturday Mohamed Nazarudeen 8903902178 Watsapp and call Sai Santosh 8925722891 watsapp and call Hashrithaa 9894654083 watsapp and call Karthick 9626985448 watsapp and call Ranjitha 8807618852 watsapp and call Surendearan 9600183612 WatsApp and call praveen 9655581000 WatsApp only 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 9655581000 Kinldy share this to all friends who in need of jobs in Coding

Hi All interview Started For CODERS & QA and offer Relese also Started Surgery Coding -1 year Above To JOIN WATSAPP GROUP PING TO 9655581000 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 Our supporting HR - Details Call Them Schedule Your Interviews Available Timing from 10.30 am to 6.30 pm Monday to Saturday Mohamed Nazarudeen 8903902178 Watsapp and call Sai Santosh 8925722891 watsapp and call Hashrithaa 9894654083 watsapp and call Karthick 9626985448 watsapp and call Ranjitha 8807618852 watsapp and call Surendearan 9600183612 WatsApp and call praveen 9655581000 WatsApp only 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 9655581000 Kinldy share this to all friends who in need of jobs in Coding

Hi All interview Started For CODERS & QA and offer Relese also Started Coding Denials (Multispeciality) - 1 year Above To JOIN WATSAPP GROUP PING TO 9655581000 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 Our supporting HR - Details Call Them Schedule Your Interviews Available Timing from 10.30 am to 6.30 pm Monday to Saturday Mohamed Nazarudeen 8903902178 Watsapp and call Sai Santosh 8925722891 watsapp and call Hashrithaa 9894654083 watsapp and call Karthick 9626985448 watsapp and call Ranjitha 8807618852 watsapp and call Surendearan 9600183612 WatsApp and call praveen 9655581000 WatsApp only 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 9655581000 Kinldy share this to all friends who in need of jobs in Coding

Hi All interview Started For CODERS & QA and offer Relese also Started EM IP +OP + Hospitalist - 1 year Above To JOIN WATSAPP GROUP PING TO 9655581000 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 Our supporting HR - Details Call Them Schedule Your Interviews Available Timing from 10.30 am to 6.30 pm Monday to Saturday Mohamed Nazarudeen 8903902178 Watsapp and call Sai Santosh 8925722891 watsapp and call Hashrithaa 9894654083 watsapp and call Karthick 9626985448 watsapp and call Ranjitha 8807618852 watsapp and call Surendearan 9600183612 WatsApp and call praveen 9655581000 WatsApp only 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 9655581000 Kinldy share this to all friends who in need of jobs in Coding