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Skill required: Marketing Operations - Digital Project Management Designation: Product Management Specialist Qualifications: Any Graduation Years of Experience: 7 to 11 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? The Project Manager – Product Line will lead a team of Product Line Specialists responsible for managing labelling, compliance, and new product introductions across regions. This role ensures consistent delivery of high-quality, compliant campaigns and projects in line with regulatory requirements, internal standards, and market timelines. It involves stakeholder management, process governance, risk mitigation, and continuous improvement in a fast-paced, cross-functional environment. Key Objectives: Understand market requirements for product launches and labelling activities; cascade tasks across the product line team. Lead end-to-end project execution, ensuring quality, compliance, and timely delivery. Manage and triage incoming work requests (tickets) and assign tasks efficiently across teams. Ensure compliance with regulatory standards and data privacy requirements across all deliverables. Drive stakeholder communication, risk mitigation, and performance tracking across all product line initiatives. Champion continuous improvement, process adherence, and metrics tracking throughout campaign and product journeys. What are we looking for? Bachelor s degree in Marketing, Business, Science, or related field. 5+ years of experience in project management, ideally in regulated industries (e.g., FMCG, pharma, chemicals). Strong leadership experience with cross-functional or remote teams. Proficiency in using project and campaign management tools (e.g., JIRA, Workfront, D365). Proven ability to manage multiple projects, meet tight deadlines, and deliver with high attention to detail. Strong communication and stakeholder management skills. Experience in product line or portfolio management is a plus. PMP, Prince2, or other relevant project management certifications. Familiarity with compliance, labelling systems, or ERP tools like SAP or Fusion is advantageous. Roles and Responsibilities: Team & Project Leadership: Lead and mentor a team of Product Line Specialists. Monitor team workload, allocate tasks, and provide guidance on priority projects. Ensure adherence to processes, SLA timelines, and documentation standards across projects. Project & Campaign Management: Own the planning, execution, and reporting of projects involving labelling, product introductions, and product changes. Manage campaign/project timelines, risks, and interdependencies across departments (Marketing, Compliance, Technology, Supply Chain). Coordinate with global and regional teams to ensure harmonized delivery. Oversee maintenance of labeling records, artwork reviews, SKU readiness, and documentation (e.g., MTT, TT, SDS). Stakeholder & Communication Management: Act as the primary point of contact for internal stakeholders, including PU Marketing Managers, Operations, Technology, GBS, and Compliance. Provide proactive communication and updates on project status, escalations, and dependencies. Compliance & Quality Assurance: Ensure all deliverables align with regulatory requirements, internal brand policies, and quality standards. Track metrics for campaign quality, compliance, and timely delivery. Drive audit-readiness and documentation traceability for all product line activities. Process & Tool Enablement: Utilize platforms such as JIRA, Workfront, Microsoft D365, or similar for ticket triaging, work orchestration, and reporting. Monitor team performance using dashboards and workflow tools; escalate issues and propose process improvements. Suggest and implement automation or digital enhancements where applicable. Any Graduation Show more Show less

Skill required: Marketing Operations - Product Requirement Definition Designation: Product Management Specialist Qualifications: Any Graduation Years of Experience: 7 to 11 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? The Labelling SME will act as the subject matter authority for all aspects of product labelling. This role ensures accurate, compliant, and cost-effective label creation, modification, and deployment by providing deep expertise in label types, processes, systems, and regulatory standards. The SME will serve as a central point of knowledge for labelling best practices and support the end-to-end product launch and change management lifecycle across regions. What are we looking for? Skill / Competency Level Labelling Accuracy & Detail Orientation Advanced Systems Knowledge (Fusion, ABC, etc.) Advanced Label Regulatory & Compliance Awareness Solid Stakeholder Communication & Alignment Advanced BOM and Product-Pack Configuration Advanced Process Execution & Standard Work Solid Cross-Functional Collaboration Essential Project Task Ownership Strong Documentation & Workflow Support Proficient Microsoft Office Tools Proficient Multilingual Communication (EU) Preferred Proven experience or expertise of 8 to 9 years in product labelling within manufacturing, packaging, or FMCG. Strong understanding of label construction, application, compliance, and cost management. Hands-on experience with tools such as Fusion, Veraciti, ABC, and Streamline. Familiarity with plant and distribution operations, BOMs, and pack-to-label mappings. Excellent English communication skills; additional European languages (Spanish, French, German) are a plus. Highly organized, a fast learner, and comfortable working in cross-functional teams. Bachelor s degree in a relevant discipline preferred (e.g. Engineering, Supply Chain, Business, Packaging Technology). Roles and Responsibilities: Key Responsibilities: Technical Expertise & Labelling Governance Provide subject matter expertise on the use and creation of all label types (top label, carton label, front/back label, OEM labels). Guide stakeholders on when and where to use specific labels based on pack type, product, and market requirements. Understand and explain the construct and cost implications of different label components, e.g. lock position, pricing families. Ensure accuracy and compliance when creating new labels from scratch or modifying existing ones. Advise on constraints and feasibility regarding SKU versioning, p-code versioning, and SKU splits. Systems & Process Management Demonstrate expertise in tools such as ABC, Fusion, Veracity, and Streamline for label creation and management. Support team members in locating and interpreting SDS (Safety Data Sheets) and PDS (Product Data Sheets). Understand and advise on the Bill of Materials (BOM) and how labelling ties into supply chain, plant, and distribution workflows. Provide input into process improvement and help build standard work instructions or documentation. Stakeholder Support & Project Involvement Work closely with artwork agencies, marketing, supply chain, compliance, and operations to ensure label integrity. Influence decisions related to labelling during product introductions, transitions, and packaging projects. Provide timely warnings or recommendations when proposed changes may impact costs, compliance, or manufacturability. Support the project team beyond labelling, offering expertise that contributes to the overall success of initiatives. Any Graduation Show more Show less

Use Your Power for Purpose At Pfizer, we believe that every role contributes to our mission of improving patients' lives. Whether you are involved in the design and development of manufacturing processes for products or supporting the upkeep of systems, engineering is crucial to ensuring customers and patients receive the medicines they need. By collaborating with our forward-thinking engineering team, you'll play a pivotal role in accelerating the delivery of medicines to the world. Automation Engineer will have responsibility for managing regulatory aspects of the process automation and control systems used in the manufacture of sterile injectable. This position will provide engineering and technical support related to the operation, maintenance, installation, startup/commissioning, testing, and qualification of manufacturing equipment and systems within a sterile injectable manufacturing facility. What You Will Achieve In this role, you will: Support the operation and troubleshooting of manufacturing equipment and control systems including DeltaV DCS, SCADA & PLCs. Support reliability engineering for production and support equipment Provide on the floor operational support as needed Support all investigations and audits as needed pertaining to automation subject matter. Responsible for Periodic review of the Automation Systems with support of validation team. Responsibility for managing regulatory aspects of the site networked engineering data collection, monitoring and SCADA systems Responsible for implementation of compliance initiatives including monitoring of system security procedures and practices and system logins for compliance Generate user requirement specifications for control systems. Author and/or review design documents for projects and process changes Define requirements for vendor design documentation. Review vendor automation design documentation (FS, HDS, SDS, DDS, requirements traceability matrix, code and logic, etc.). Support FAT/commissioning/qualification activities as required Review qualification protocols of automated systems. Support the execution of the qualification of automated control systems. Prepare risk assessments for automated systems Prepare Change Controls associated with changes to control systems Design and implementation support for functional and process changes, either smaller projects, remediation activities or capital projects Support future capital projects and assure site automation standards are followed Assist other departments in evaluating historical process/equipment data Provide automation guidance and training to other functional groups (i.e. Operations, Validation, Maintenance, QA, etc.) Responsible for backup/archiving/restoring of Automation configuration and batch. Understand 21 CFR Part 11, cGAMP, and other regulatory guidance associated with computer / automation-based systems. Develop and implement site automation standards for hardware and software Develop automation Standard Operating Procedures Here Is What You Need (Minimum Requirements) Bachelor of Technology/Engineering in Electronics/Instrumentation Engineering 6 to 8 years’ experience in a combination of process control, automation (PLC, SCADA & DCS) in pharmaceuticals, biotechnology or other life sciences industries. Individual must be capable of reading and understanding electrical control system diagrams (control panel wiring diagrams, loop drawings, panel layout drawings and schedules, etc.). Comfortable walking down control system diagrams and red lining them to reflect as built conditions. Good technical knowledge on field Instrumentation Good technical knowledge of industrial communication networks and related hardware & software. Basic understanding of sequel servers and databases. Familiarity with current industry practices and guidelines including those required / outlined by the FDA, ISO, EU and ICH. Bonus Points If You Have (Preferred Requirements) Relevant pharmaceutical experience Understanding of programming and proficiency in at least one language Knowledge of Good Manufacturing Practices (GMP) Ability to train others effectively Strong problem-solving skills Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Engineering Show more Show less

Use Your Power for Purpose Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring customers and patients receive the medicines they need, precisely when they need them. By collaborating with our forward-thinking engineering team, you'll play a key role in accelerating the delivery of medicines to the world. Your innovative ideas and proactive actions will help us imagine new possibilities and bring them to life, making a significant impact on global health. As an Associate in the Global Supply division, you will contribute to improving patients' lives while working at Pfizer. Your dedication and expertise will ensure our plants, utility systems, buildings, and equipment are operational, helping us achieve new milestones and assist patients worldwide. What You Will Achieve In this role, you will: Support the operation and troubleshooting of manufacturing equipment and control systems including DeltaV DCS, SCADA & PLCs. Should work in shifts to provide operational support on Automated systems. Support all investigations and audits as needed pertaining to automation subject matter. Responsible for Periodic review of the Automation Systems with support of validation team. Responsible for implementation of compliance initiatives including monitoring of system security procedures and practices and system logins for compliance Generate user requirement specifications for control systems. Author and/or review design documents for projects and process changes Define requirements for vendor design documentation. Review vendor automation design documentation (FS, HDS, SDS, DDS, requirements traceability matrix, code and logic, etc. Execute qualification protocols of automated systems. Prepare risk assessments for automated systems Prepare Change Controls associated with changes to control systems Design and implementation support for functional and process changes, either smaller projects, remediation activities or capital projects Responsible for backup/archiving/restoring of Automation configuration and batch. Understand 21 CFR Part 11, cGAMP, and other regulatory guidance associated with computer / automation-based systems. Develop automation Standard Operating Procedures Here Is What You Need (Minimum Requirements) Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience in Instrumentation/Electronics/Computers. Experience in DeltaV DCS, other DCS, SCADA and PLC based systems. Demonstrated ability to write and provide simple and accurate instructions Working experience in pharmaceutical industry Demonstrated computer and technical skills Effective problem-solving capabilities Excellent interpersonal communication and written skills Bonus Points If You Have (Preferred Requirements) Knowledge or experience working in a Good Manufacturing Practices (also cGMP) environment Strong organizational skills Ability to work independently and as part of a team Proactive and self-motivated Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Engineering Show more Show less

Looking for any Certified/Non-Certified Medical coder IPDRG/ Coder/QA ED Coder/QA/SME Surgery Coder/QA/SME Both Work From Home and Work From Office is available. Preferably Immediate Joinees or 15 days Flexible in Relieving letters & Gaps. Required Candidate profile Looking for Certified/Non Certified Medical coder with any specialty like IPDRG CODER/SR.CODER/QA ED Coder/QA Surgery Coder/QA

Looking for any Certified/Non-Certified Medical coder IPDRG/ Coder/QA Anesthesia Coder/QA/SME Surgery Coder/QA/SME Both Work From Home and Work From Office is available. Preferably Immediate Joinees or 15 days Flexible in Relieving letters & Gaps. Required Candidate profile Looking for Certified/Non Certified Medical coder with any specialty like IPDRG CODER/SR.CODER/QA Anesthesia Coder/QA Surgery Coder/QA

Looking for any Certified/Non-Certified Medical coder IPDRG/ Coder/QA Anesthesia Coder/QA/SME Home Health Coder/QA/SME Both Work From Home and Work From Office is available. Preferably Immediate Joinees or 15 days Flexible in Relieving letters & Gaps Required Candidate profile Looking for Certified/Non Certified Medical coder with any specialty like IPDRG CODER/SR.CODER/QA Anesthesia Coder/QA Home Health Coder/QA

Looking for any Certified/Non-Certified Medical coder IPDRG/ Coder/QA Anesthesia Coder/QA/SME Surgery Coder/QA/SME Both Work From Home and Work From Office is available. Preferably Immediate Joinees or 15 days Flexible in Relieving letters & Gaps. Required Candidate profile Looking for Certified/Non Certified Medical coder with any specialty like IPDRG CODER/SR.CODER/QA Anesthesia Coder/QA Surgery Coder/QA

Looking for any Certified/Non-Certified Medical coder IPDRG/HHC Coder/QA Pathology Coder/QA/SME Surgery Coder/QA/SME Both Work From Home and Work From Office is available. Preferably Immediate Joinees or 15 days Flexible in Relieving letters & Gaps. Required Candidate profile Looking for Certified/Non Certified Medical coder with any specialty like IPDRG CODER/SR.CODER/QA HHC Coder/QA Anesthesia Coder/QA Surgery Coder/QA

*Greetings from Access Healthcare* Openings for Senior Medical Coders 1. Surgery Coder ( WFO/WFH ) - Chennai & Coimbatore & Pune 2. *Denials coder* ( WFO /WFH) - Chennai, Coimbatore & Pune 3. *Em op coder*( WFO) - Chennai & Coimbatore & Pune 4. *IVR Coder*( WFO) - Chennai & Coimbatore 5. *Ed facility* - Chennai& Coimbatore & Pune ( WFO /WFH) 6. Radiology coder -Chennai and coimbatore & Pune Certified only Exp - 1+ yrs Immediate joiners only. Sudharsun - 9941195485.

Role & responsibilities Hiring For Medical Coders || ED Facility, ED Blended, ED Profee, ENM OP& IP, Surgery, Radiology , Denials Multispeciality || Upto 10 LPA || Work From Office Location :- Hyderabad, Chennai Work From Office Day Shift 2 WAY Cab facility Specialties :- 1. ENM OP & IP - Chennai || Already Serving notice 2. ED Facility - Chennai || Already Serving notice 3. ED Blended - Chennai 4. Denials Multispeciality - Hyderabad, Chennai 5. Surgery Coder - Hyderabad, Chennai 6.Radiology - Chennai 7. ENM with Surgery Min 1+ year experience into the above Speciality is mandate Package :- Upto 10 LPA Only Certified Notice period:- 0 - 2 months Interested candidates can share your updated resume to HR Shruthi - 7680001201 (share resume via WhatsApp ) saishruthi.axisservices@gmail.com Refer ur friends/collegues Perks and benefits Day Shift 2 way cab

Hiring for Ipdrg Coder and QA, General surgery and SDS QA and coder Minimum of 1.5 yrs years of experience Location- Chennai US shifts Work from Office salary Negotiable Roles and Responsibilities: - Accurately code SDS and Special Procedures through review of medical record documentation and encounter forms for Outpatient facility General surgery and SDS QA and coder vacancy Hands on experience in coding tools such as EPIC, 3M, Optum. Assign CPT procedure codes, ICD-10 diagnosis codes, and modifiers based on documentation, government teaching physician documentation requirements and LCD/NCD/ NCCI policies. Should have working experience in all Surgery procedures (10000-69990 CPT series) Good knowledge in Cardiac catheterization with 9xxxx series codes is an added advantage. Minimum of 1.5 yrs years of experience Basic knowledge of medical terminology and anatomy. Comfortable to work from office. Effective verbal and written communication skills (Should have capability to reply properly to client and stakeholders. Successful completion of CPC or CCS certification must be active during joining and verified. Able to work independently and willing to adapt and change as per business/ process requirements. Please call Durga 9884244311 for more Info Regards Durga 9884244311

Senior Medical coder Specialty : Ed profee &Facility , Surgery Coding Both Certified and Non certified Work Location: Chennai , Trichy , Salem Experience Required: 1 to 5 years Job Responsibilities: We are looking for a Medical Coder to join our team to assist us in coding for insurance claims and databases. The Medical Coder will display motivation, be detail-oriented and have outstanding people skills that help them navigate any situation with ease. Responsibilities: Account for coding and abstracting of patient encounters Research and analyze data needs for reimbursement Make sure that codes are sequenced according to government and insurance regulations Ensure all medical records are filed and processed correctly Analyze medical records and identify documentation deficiencies Serve as resource and subject matter expert to other coding staff Review and verify documentation for diagnoses, procedures and treatment results Identify diagnostic and procedural information Required Skills & Qualifications: Coding Knowledge Familiarity with CPT, ICD-10, and HCPCS codes. Experience in RCM (Revenue Cycle Management) Perks and Benefits: Competitive salary and incentives Training and career growth opportunities Supportive work environment Apply Now! Don't Miss This Exciting Opportunity! Interested Candidate share Update Resume : Nivetha HR @ 7200450038 aashwiny.gopi@jobixoindia.com

Hi All interview Started For CODERS & QA and offer Relese also Started Anesthesia -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 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 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 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

Hi All interview Started For CODERS & QA and offer Relese also Started ED Profee Facility + Ancillary - 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 OP - 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 Denial Coder - 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 HCC Coders - 2 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 HCC 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

Skill required: Marketing Operations - Product Requirement Definition Designation: Product Management Senior Analyst Qualifications: Any Graduation Years of Experience: 5 to 8 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? The Labelling SME will act as the subject matter authority for all aspects of product labelling. This role ensures accurate, compliant, and cost-effective label creation, modification, and deployment by providing deep expertise in label types, processes, systems, and regulatory standards. The SME will serve as a central point of knowledge for labelling best practices and support the end-to-end product launch and change management lifecycle across regions. What are we looking for? Skill / Competency Level Labelling Accuracy & Detail Orientation Advanced Systems Knowledge (Fusion, ABC, etc.) Advanced Label Regulatory & Compliance Awareness Solid Stakeholder Communication & Alignment Advanced BOM and Product-Pack Configuration Advanced Process Execution & Standard Work Solid Cross-Functional Collaboration Essential Project Task Ownership Strong Documentation & Workflow Support Proficient Microsoft Office Tools Proficient Multilingual Communication (EU) Preferred Proven experience or expertise of 6 to 7 years in product labelling within manufacturing, packaging, or FMCG. Strong understanding of label construction, application, compliance, and cost management. Hands-on experience with tools such as Fusion, Veraciti, ABC, and Streamline. Familiarity with plant and distribution operations, BOMs, and pack-to-label mappings. Excellent English communication skills; additional European languages (Spanish, French, German) are a plus. Highly organized, a fast learner, and comfortable working in cross-functional teams. Bachelor s degree in a relevant discipline preferred (e.g. Engineering, Supply Chain, Business, Packaging Technology). Roles and Responsibilities: Technical Expertise & Labelling Governance Provide subject matter expertise on the use and creation of all label types (top label, carton label, front/back label, OEM labels). Guide stakeholders on when and where to use specific labels based on pack type, product, and market requirements. Understand and explain the construct and cost implications of different label components, e.g. lock position, pricing families. Ensure accuracy and compliance when creating new labels from scratch or modifying existing ones. Advise on constraints and feasibility regarding SKU versioning, p-code versioning, and SKU splits. Systems & Process Management Demonstrate expertise in tools such as ABC, Fusion, Veracity, and Streamline for label creation and management. Support team members in locating and interpreting SDS (Safety Data Sheets) and PDS (Product Data Sheets). Understand and advise on the Bill of Materials (BOM) and how labelling ties into supply chain, plant, and distribution workflows. Provide input into process improvement and help build standard work instructions or documentation. Stakeholder Support & Project Involvement Work closely with artwork agencies, marketing, supply chain, compliance, and operations to ensure label integrity. Influence decisions related to labelling during product introductions, transitions, and packaging projects. Provide timely warnings or recommendations when proposed changes may impact costs, compliance, or manufacturability. Support the project team beyond labelling, offering expertise that contributes to the overall success of initiatives. Any Graduation Show more Show less

Company Description 4XStruct takes pride in delivering exceptional services even under tight deadlines, utilizing a technology-driven approach. With over 20 years of experience in structural steel detailing, fabrication, branding, operations, and project management, our leadership and management team promotes distinctiveness, efficiency, and innovation in their offerings. We invest heavily in training our staff to ensure they are equipped with the latest tools, techniques, and knowledge, allowing us to adapt to evolving client needs and advancements in technology. At 4XStruct, we view our workforce as a vital asset, enhancing client retention and stimulating business growth. Role Description This is a full-time on-site role located in Nashik for Tekla and SDS Experts. The primary responsibilities include utilizing Tekla and SDS software for structural steel detailing, generating accurate 3D models and drawings, reviewing and coordinating designs for fabrication, ensuring compliance with industry standards, and collaborating closely with internal teams and clients to ensure project specifications are met. Additional tasks include troubleshooting and resolving software-related issues, providing technical support, and continuously exploring new methodologies to improve efficiency and accuracy. Qualifications Proficiency in using Tekla and SDS software for structural steel detailing Experience in generating 3D models and producing detailed drawings Strong ability to review, coordinate, and ensure compliance with industry standards Excellent technical support and troubleshooting skills Effective communication and collaboration skills Ability to work independently and manage multiple projects simultaneously Relevant certifications in Tekla or SDS software are a plus Bachelor's degree or Diploma in Civil Engineering, Structural Engineering, or related field is preferred Show more Show less