Surgery Coder (MC) - Surgery Coding Hyderabad, Telangana Medical Coding Description nimble solutions is a leading provider of revenue cycle management solutions for ambulatory surgery centers (ASCs), surgical clinics, surgical hospitals, and anesthesia groups. Our tech-enabled solutions allow surgical organizations to streamline their revenue cycle processes, reduce administrative burden, and improve financial outcomes. Join more than 1,100 surgical organizations who trust nimble solutions and its advisors to bring deep insights and actionable intelligence to maximize their revenue cycle. In the role of Medical Coder, this individual will be responsible for the following: Perform a variety of activities involving the coding of medical records by ascribing accurate diagnosis and CPT codes as per ICD-10 and CPT-4 systems of coding Perform Coding for records pertaining to surgeries performed with a minimum of 96% accuracy and as per turnaround time requirements Exceeds the productivity standards for Medical Coding for Surgery - as per the productivity norms for inpatient and/or specialty specific outpatient coding standards Maintains high degree of professional and ethical standards Focuses on continuous improvement by working on projects that enables customers to arrest revenue leakage while being in compliance with the standards Focuses on updating coding skills, knowledge, and accuracy by participating in coding team meetings and educational conferences Requirements To be considered for this position, applicants need to meet the following qualification criteria: Graduates in life sciences with 2 - 8 years of experience in Medical Coding for Surgery specialty Experience in Surgery coding is required Exposure to CPT-4, ICD-9 and ICD-10 Certification is not mandatory Good knowledge of medical coding systems and regulatory requirements

Medical Coder : Open position - Specialty Surgery coder, Home Health, ED profee, E/M Op IP, Ipdrg coder, E/M QC Location : Chennai, Bangalore ( WFO ) Experience : Min 1+ year experience coding mandatory contact 6379093874 ( Sangeetha S) what's app

Preferred candidate profile Surgery Coders : Should carry 2+ yrs experience in surgery coding Should be AAPC certified Work from office for initial 4 months Immediate joiners or 15 days notice period is preferred Surgery QAs : Should carry 6+ yrs experience in surgery coding Should carry minimum 1 year experience on paper as QA Acting QAs can also apply for the requirement Should be AAPC certified Work from office for initial 4 months Immediate joiners or 15 days notice period is preferred Note: Eligible for 25k Joining Bonus if joined on or before 15th June'25 Suitable candidates can send updated CV'S on WhatsApp : 8121002992 Regards Human Resources Eclat Health Solutions India Pvt Ltd

Dear Candidates, Greetings from Teleperformance!!! Candidates should have minimum 1 year experience in surgery coding. Certification is Not Mandatory. Should be graduate. 5 days working (5.30 pm to 2.30 am and 7.00 am to 4 .00 pm) Saturday and Sunday Fixed week off. Looking for immediate joiners. Job Location - Ambattur- Ambit IT Park Salary up to 6.50 LPA Interested candidates Please call Hema @ 8524862257. Regards Hema Assistant Manager

We are seeking a motivated Biotechnology Associate to join our Product Development and Field Support Team . This role involves hands-on work in kit preparation, ELISA, electrophoresis, DNA/protein extraction, troubleshooting , and client interactions across India. You will contribute to developing high-quality biotech kits while providing on-site technical support to clients. Key Responsibilities1. Laboratory Work & Kit Development Prepare and optimize biotechnology kits (e.g., DNA/RNA extraction, protein purification). Design and perform ELISA assays , gel electrophoresis (SDS-PAGE, agarose) , Cell culture and chromatography . Conduct quality control (QC) tests on reagents and kits. Troubleshoot technical issues in sample processing, extraction, and assay workflows . 2. Field Support & Client Management Travel to client sites (labs, hospitals, research centers) across India for product demonstrations, training, and troubleshooting . Build and maintain strong relationships with academic, clinical, and industrial clients . Gather customer feedback to improve product design and usability. 3. Documentation & Compliance Maintain detailed records of experimental protocols, QC data, and client reports . Ensure compliance with ISO or other regulatory standards (if applicable). 4. Cross-Functional Collaboration Work with R&D, manufacturing, and sales teams to refine product workflows. Attend scientific conferences, exhibitions, and networking events to promote products. Qualifications & SkillsEssential: Bachelor’s/Master’s degree in Biotechnology, Biochemistry, Molecular Biology, or related field . Hands-on experience with: DNA/RNA extraction (e.g., column-based, magnetic bead kits). ELISA (indirect, sandwich, competitive). Cell Culture Electrophoresis (agarose, SDS-PAGE). Protein purification (TFF, affinity chromatography). Strong analytical and troubleshooting skills . Willingness to travel up to 40% (client visits across India). Preferred: Familiarity with PCR, qPCR, or NGS workflows . Experience in IVD kit development (diagnostics). Knowledge of regulatory standards (ISO 13485, GMP). Fluency in English + regional Indian languages (Hindi, Tamil, etc.). Work Place: IIDC KOSI KOTWAN, NABIPUR Mathura, Uttar Pradesh, 281403 Job Types: Full-time, Permanent Pay: ₹9,154.29 - ₹22,928.79 per month Schedule: Fixed shift Monday to Friday Morning shift Ability to commute/relocate: Mathura, UP: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Minimum Salary Expectation: Work Location: Hybrid remote in Mathura, UP

Job Purpose JOB DESCRIPTION To ensure compliance of computerized systems, PLC/SCADA-controlled equipment, and automation systems with regulatory requirements (21 CFR Part 11, EU Annex 11, GAMP 5, etc.) by executing validation activities as per approved procedures and maintaining validated states throughout the system lifecycle. Key Responsibilities Validation Planning & Execution: Develop and maintain validation protocols (URS, DQ, IQ, OQ, PQ, RTM) for computerized systems and PLC/SCADA-controlled equipment. Execute validation activities in line with cGMP, GAMP 5, and internal SOPs. Review and approve vendor-supplied documentation (FDS, HDS, SDS, FAT/SAT, etc.). Compliance & Documentation Ensure systems comply with 21 CFR Part 11 and data integrity principles. Maintain proper documentation and traceability of all validation activities. Prepare validation summary reports and maintain system validation status. Risk Assessment & Change Management Conduct risk assessments for new or modified systems and automation projects. Participate in impact assessments and manage change control for validated systems. Audit Support & Training Support internal and external audits (USFDA, MHRA, EU, WHO, etc.). Provide training and guidance to users and departments on validated systems and data integrity practices. Coordination & Vendor Management Coordinate with Engineering, IT, QA, QC, Production, and vendors for validation-related activities. Monitor vendor performance and ensure timely completion of qualification activities. Lifecycle Management Ensure systems remain in a validated state through periodic reviews and re-validation as needed. Support decommissioning and archival activities as per SOPs. Key Skills And Competencies Strong knowledge of CSV principles, GAMP 5, 21 CFR Part 11, and Annex 11. Familiarity with PLCs, SCADA, HMI, DCS, MES, and Building Management Systems (BMS). Understanding of pharmaceutical manufacturing processes and regulatory requirements. Good documentation, analytical, and problem-solving skills. Effective communication and project coordination abilities. Qualifications Qualification: B.Pharma/ M.Pharma/ B.E / B.Tech Candidate must have 3 - 5 years of relevant experience. Note: Employee who want to apply for internal job posting must have completed atleast 2 years in his current role. Show more Show less

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com Job Function Data Analytics & Computational Sciences Job Sub Function Biostatistics Job Category Scientific/Technology All Job Posting Locations: PENJERLA, Telangana, India Job Description Position Summary The Principal Statistician supports the design, execution, analysis, interpretation, and reporting or communication of data evidence for Pre/Early/Late Clinical Development, Research & Discovery, Medical Affairs, Real World Evidence, or Manufacturing Sciences programs for research, development, and/or marketed product needs in Janssen, with minimal supervision. This position supports statistical aspects of business-critical and/or regulatory commitments, provides input to program plans with limited supervision, and represents Statistics & Decision Sciences (SDS) for cross-functional and intra-departmental teams or working groups. He/She abides by the Credo and practices J&J Leadership Imperatives for Individuals: Lead, Shape, Connect, and Deliver. Position Core Competencies, Responsibilities And Accountabilities Expertise: Demonstrates advanced data analytic expertise based on a foundation of statistical principles and a strong track record of applied experience leading to successful program support. Is effective in the use of relevant computational tools for study, experiment, or trial research objectives. Applies high quality statistical methodology in assigned projects with demonstrated understanding of the disease/scientific/functional area and health authority acceptability. Quality and Compliance: Complies with organization and company standard operating procedures in timely fashion, such as training and project time accounting. Understands and aligns with relevant regulatory guidances. Contributes high quality and timely deliverables as assessed by stakeholders such as the project team, the clinical trial team, and the Statistics Area Head. Ensures that documents, specifications, programs, and macros are consistent and comply with project and company standards. Follows best practices for Data Integrity. Drug Development : Demonstrates thorough knowledge of pharmaceutical research and development strategies and execution. Takes a lead in providing SDS support to experimental design, modeling, analysis planning, analysis execution, interpretation, and statistical communications. Is accountable for execution of individual project responsibilities, including: meetings with necessary project team members, reporting activities, exploratory analyses/graphics, and additional analyses to support publications for individual clinical trials/studies/projects. Is an evolving leader for providing input to team in terms of optimizing study or trial designs in line with study or indication level objectives, and supports scenario simulations and sample size calculations based on relevant technical and disease/scientific/functional area knowledge. Disease Area Knowledge: Demonstrates knowledge for at least one disease area/target . Innovation: Suggests and performs the evaluation of alternative or innovative approaches to statistical methods or business processes. Representation: Represents Statistics & Decision Sciences for cross-functional and intra-departmental teams or working groups relating to scientific or process initiatives. External Engagement: Participates as a member of professional organizations, e.g. by attending meetings as chair or presenter. Mentor: Supervises contractors/special assignment personnel/interns/co-ops as required. Mentors junior colleagues in techniques, processes, and responsibilities. Process: Participates in process improvement or standards development initiatives. Complexity: Works on increasingly more complex programs after mastering standard ones. Proactively identifies complexity in terms Scientific, Statistical, Health Authority, Operational, and Partnership issues. Collaboration: Builds cross-functional partnerships with internal colleagues and with external partners (e.g. Contract Research Organizations (CROs), consultants) to achieve results for project specific needs with focus on improving communication, efficiency, and productivity. Works cross-functionally to identify and resolve issues. Communication: Has very good written, oral, and interpersonal communication skills. Demonstrated ability to collaborate and consult with non-statisticians, translating complex statistical concepts to drug research & development partners. Bridges scientific and business needs – integrating quantitative sciences and strong disease or functional area knowledge and appropriate market/competitive intelligence. Programming: Demonstrates full proficiency in SAS or R, as well as a working knowledge of other relevant computational tools as required. Area Specific Core Competencies, Responsibilities And Accountabilities These are additional to the above position core competencies, applicable to individuals according to their assigned area within Statistics & Decision Sciences. Discovery & Translational Documents projects in sufficient detail for reproducibility. Serves as initial consultation contact for new projects. Maintains and grows customer base, and builds loyal relationships with customers. Assumes independent, professional responsibility for all phases of a project request from beginning through completion, with minimal supervision as needed. Manages multiple projects. Leads Statistical Input for at least one functional area, research field, or compound. Provides input to product development and performs statistical functions for submission related activities where appropriate. Statistical Modeling & Methodology Support broad implementation of innovative statistical approaches across the development portfolio. Support development and implementation of innovative approaches, participating in their hands-on implementation through direct interactions with statisticians. This involves, but is not limited to, identifying appropriate designs and methods, decision rules (e.g., Go/No Go); planning, running, and summarizing simulation studies to evaluate the operating characteristics of alternative designs and methods under a range of scenarios; and participating in the implementation of the selected approaches by engaging in protocol and SAP write-up. Collaborate with external consultants to provide support in the development and implementation of innovative methods and designs. Identify opportunities for innovation; interact directly with statisticians and other QS scientists for early identification of opportunities for innovative approaches. Participate in training and presentations on innovative approaches across the R&D organization (including statisticians, pharmacometricians, clinicians, and other stakeholder groups) to ensure awareness and adequate knowledge about these methods. Keep up-to-date knowledge of designs and analysis methods for clinical trials, including adaptive designs, model-based methods, etc. May engage in external collaborations within professional associations (e.g., ASA, IBS, SCT, ISoP, ISCB, PSI, EFPSI), participating in working groups, program committees, organizing sessions and presenting at scientific meetings, and publishing in peer reviewed journals. Knowledge of biostatistics applied to clinical trials and model-based drug development. Some experience with planning, running, and documenting simulations (including, but not limited to clinical trial simulations). Awareness of Bayesian methods and inference. Manufacturing & Toxicology Documents projects in sufficient detail for reproducibility, including entry in project tracking systems and placement into shared repositories. Serves as initial consultation contact for new projects. Maintains and grows customer base, and builds loyal relationships with customers. Assumes independent, professional responsibility for all phases of a project request from beginning through completion, with minimal supervision as needed. Manages multiple projects. Leads Statistical Input for at least one functional area, research field, or compound. Provides input to product development and performs statistical functions for submission related activities where appropriate. Medical Affairs Provides critical statistical oversight to Medical Affairs clinical studies and assumes a leadership role in clinical trial and/or patient registries planning (mostly Phase 3b/4 trials or observational studies for post marketing commitments/requirements) and reporting related activities; assumes the role of a Statistics representative for cross-functional teams and works on several trials (projects) simultaneously. Provides statistical input for clinical trials, observational studies and other types of clinical research projects including but not limited to post-hoc analyses, investigator initiated studies, publications, and HECOR/Epidemiology/Market Access support; Contributes/leads clinical study design, analysis planning and for the development of statistical analysis plan (SAP) and data presentation plan (DPS) for MA studies; Provides input to product development and performs statistical functions for submission related activities; Provides statistical support to other disciplines related to clinical statistics (e.g., HECOR/Epidemiology and publication activities); May serve as a primary contact with outside investigators (and vendors)in the preparation of scientific presentations and manuscripts; may interact with external Key Opinion Leaders (KOLs) and pursues rigorous statistical analyses in support of business-critical new research ideas; Explores and implements innovative statistical methods; Represents department in meetings with regulatory agencies. Real World Evidence Proactively interface with clinical teams to identify opportunities where real-world data analysis can support the clinical development feasibility assessment; Serve as liaison between the TA Clinical Teams and the Epidemiology Analytics Team to facilitate the translation of protocol Inclusion/Exclusion criteria into meaningful data definitions, and to track and measure outcomes; Work with RWE Feasibility Lead to shape and influence the future of protocol development through the use of novel technology applied to real world data to enhance data-driven operational decision making; Work closely with key stakeholders, including the Study Placement & Analytics group and the Clinical Program Leader, to run RWE analysis that support protocol design and protocol feasibility. Supervision and Reporting Relationships This position reports to a Director or above, and is an individual contributor position. Interfaces Internal: Statistics & Decision Sciences, Clinical Pharmacology & Pharmacometrics, Clinical Teams (or Equivalent) and associated working groups, Statistical Programming, Medical Writing, Leaders and Scientists within Therapeutic and Functional Areas, R&D Operations, Medical Affairs, Manufacturing, Safety, Regulatory Affairs, Quality, Human Resources, Information Technology, Finance. External: Contracted Partners, Academia, Professional Societies, Private and Public Consortia. Education And Experience Requirements Ph.D. in Statistics or related field with minimum 3 years relevant experience, or Master’s in Statistics or related field with commensurate years of relevant experience. Proficient in SAS or R programming. Good written, oral, and interpersonal communication skills. Ability to work independently. Demonstrated ability to work in interdisciplinary contexts outside statistics. Show more Show less

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com Job Function Data Analytics & Computational Sciences Job Sub Function Biostatistics Job Category Scientific/Technology All Job Posting Locations: PENJERLA, Telangana, India Job Description Position Summary The Senior Statistician provides statistical services including analysis, interpretation, design, and reporting or communication of data evidence for research, development, and/or marketed product needs in Janssen. This position supports statistical aspects of business-critical and/or regulatory commitments. He/She abides by the Credo and practices J&J Leadership Imperatives for Individuals: Lead, Shape, Connect, and Deliver. Position Core Competencies, Responsibilities And Accountabilities (including lower pay grade level requirements not explicitly re-stated here) Expertise: Demonstrates advanced data analytic expertise based on a foundation of statistical principles and a track record of applied experience. Is effective in the use of relevant computational tools for study, experiment, or trial research objectives. Applies high quality statistical methodology in assigned projects with demonstrated understanding of the disease/scientific/functional area and health authority acceptability. Ensures application of appropriate statistical methods and generation of accurate and reproducible results working independently or by providing specifications to statistical programming colleagues. Produces clear, concise, well-organized, and error-free computer programs and statistical reporting content. Quality and Compliance: Complies with organization and company standard operating procedures in timely fashion, such as training and project time accounting. Understands and aligns with relevant regulatory guidances. Contributes high quality and timely deliverables as assessed by stakeholders such as the project team, the clinical trial team, and the Statistics Area Head. Ensures that documents, specifications, programs, and macros are consistent and comply with project and company standards. Follows best practices for Data Integrity. Drug Development: Acquires and demonstrates knowledge in pharmaceutical research and development strategies and execution. Assists in providing experimental design, modeling, analysis planning, analysis execution, interpretation, and statistical communications support. Is accountable for execution of individual project responsibilities, including: meetings with necessary project team members, reporting activities, exploratory analyses/graphics, and additional analyses to support publications for individual clinical trials/studies/projects. Provides critical input to the statistical lead or team in optimizing study or trial designs in line with study or trial objectives, and supports scenario simulations and sample size calculations based on relevant technical and disease/scientific/functional area knowledge. Collaboration: Establishes and maintains effective and efficient interfaces and relationships with internal and external customers, with support of Statistics & Decision Sciences (SDS) management. Routinely contributes to area (e.g. discovery, translational, early development, late development) project meetings. Contributes positively to SDS team dynamics with a clear understanding of the SDS vision. Programming: Demonstrates full proficiency in SAS or R, as well as a working knowledge of other relevant computational tools as required. Process: Deep knowledge of data architecture, such as Data Standards. Recognizes the need and value of process standardization. External Engagement: Participates as a member of professional organizations, such as attending meetings sponsored by professional organizations. Area Specific Core Competencies, Responsibilities And Accountabilities These are additional to the above position core competencies, applicable to individuals according to their assigned area within Statistics & Decision Sciences. Discovery & Translational Serves as initial consultation contact for new projects. Maintains and grows customer base, and builds loyal relationships with customers. Assumes independent, professional responsibility for all phases of a project request from beginning through completion, with minimal supervision as needed. Manages multiple projects. Documents projects in sufficient detail for reproducibility. Statistical Modeling & Methodology Not Applicable. Manufacturing & Toxicology Serves as initial consultation contact for new projects. Maintains and grows customer base, and builds loyal relationships with customers. Assumes independent, professional responsibility for all phases of a project request from beginning through completion, with minimal supervision as needed. Manages multiple projects. Documents projects in sufficient detail for reproducibility, including entry in project tracking systems and placement into shared repositories. Medical Affairs Provides statistical support to Medical Affairs studies and assumes responsibilities for planning, design and analysis of randomized clinical trials, observational studies and/or patient registries for post marketing commitments/requirements and reporting related activities. Applies sound statistical thinking and computational abilities in support of Medical Affairs goals & objectives. Contributes in the planning, design, conduct and analysis for clinical trials, observational studies and other types of clinical research projects including but not limited to post-hoc analyses, investigator initiated studies, publications, and HECOR/Epidemiology/Market Access support; Develops statistical analysis plans (SAPs) and data presentation specifications (DPSs); Provides statistical support for all LCM/regulatory-submission related activities; Interacts with other Medical Affairs functional groups (e.g., HECOR/Epidemiology, Market Access and publication teams); in close partnership with statistical lead, interacts with outside investigators (KOLs and vendors) in the preparation of scientific presentations and manuscripts and pursues implementation of robust statistical analyses in support of business-critical evidence generation; Explores and implements innovative statistical methods. Real World Evidence Not Applicable. Post Marketing Surveillance (PMS) Provide advanced statistical expertise in PMS programs, study design, data analysis and interpretation of results for PMS studies. Assume independent, professional responsibilities for analysis operations. Lead study design, analysis planning and for the development of statistical analysis plan (SAP) and data presentation plan (DPS) for PMS studies. Monitor the analysis operations conducted by vendors, an oversees design and implement quality control measures to ensure the quality and integrity of statistical results. Provide consultancy for statistical questions from medical affairs/business units or external customers. Interacts with outside investigators (Key Opinion Leaders (KOLs) and vendors) in the preparation of scientific presentations and manuscripts. Implement “state‐of‐the‐art” statistical approach and technology. Contribute to the implementation of continuous process improvements while maintain sustainable efficiency in globally consistent processes, such as data standards and process standardization. Basic knowledge of project management. Supervision and Reporting Relationships This position reports to a Director or above, and is an individual contributor position. Interfaces Internal: Statistics & Decision Sciences, Clinical Pharmacology & Pharmacometrics, Clinical Teams (or Equivalent) and associated working groups, Statistical Programming, Medical Writing, Leaders and Scientists within Therapeutic and Functional Areas, R&D Operations, Medical Affairs, Manufacturing, Safety, Regulatory Affairs, Quality, Human Resources, Information Technology, Finance. External: Contracted Partners, Academia, Professional Societies, Private and Public Consortia. Education And Experience Requirements Ph.D. in Statistics or related field with minimum 0-2 years relevant experience, or Master’s in Statistics or related field with commensurate years of relevant experience. Basic knowledge of SAS or R programming. Good written, oral, and interpersonal communication skills. Show more Show less

Job Location MUMBAI GENERAL OFFICE Job Description P&G was founded over 180 years ago as a simple soap and candle company. Today, we're the world’s largest consumer goods company and home to iconic, trusted brands that make life a little bit easier in small but significant ways. We've spanned three centuries thanks to three simple ideas: leadership, innovation and citizenship. The insight, innovation and passion of hardworking teams has helped us grow into a global company that is governed responsibly and ethically, that is open and clear, and that supports good causes and protects the environment. This is a place where you can be proud to work and do something that matters. Dedication from Us : You will be at core of Ground- breaking innovations, be given exciting opportunities, lead initiatives, and take charge and responsibility, in creative workspaces where new insights thrive. All the while, you'll receive outstanding training to help you become a leader in your field. What we Offer : Continuous mentorship – work with peers and receive both formal training as well as day-to-day mentoring from your manager multifaceted and encouraging work environment– employees are at the centre, we value every individual and support initiatives, promoting agility and work/life balance. Overview Of The Job Lead indirect spend pool sourcing for a P&G India site including goods as well as services within defined spend range. Collaborate with internal as well external stakeholders to generate right value creation for the organization while ensuring service to internal stakeholders and governance throughout the sourcing process. Your team This role reports to SDS Cluster Manager Purchases & person will be located out of Mumbai, India. How Success Looks Like Value Creation – Drive exceptional impact through Value Creation in Cost & Cash in respective sourcing desk. Sufficient pipeline to be developed to meet the internal target of Cost savings / Cash as it is a critical success criterion. Stewardship & Governance – Understand the purchases policies & sourcing principles. There should not be any misses on stewardship & take necessary actions to ensure audit gaps closure. Person should be able to demonstrate & guide users on right thing to do in line with our PVPs. Simplification & User experience – Analyse the processes to identify simplification opportunities in the sourcing activities across spend pools to ensure exceptional user experience. Proactively support any business-critical situations to ensure no business risk. Productivity – Championing productivity through eliminating unnecessary, overly complex, or duplicative work/costs that do not create value. Adopt structured approach to manage daily purchases requisitions & drive effective reviews with team as well as manager. Responsibilities Of The Role Individual is expected to source Indirect goods/services (Indirect) independently for respective sites in the scope. Review open purchase requisitions on daily basis along with cluster leader & create best value for the organization. Ensure timely closure of sourcing of requisitions to avoid any impact on business continuity. Identify savings opportunities by collaborating with site stakeholders & execute to meet internal value creation targets. Collaborate with plant/site users to ensure supplier sufficiency for each commodity & identify new suppliers wherever required to facilitate the site. Ensure compliance to purchasing policies throughout the processes & correct the gaps. Job Qualifications Graduate and above with preference to prior procurement / sourcing experience of 2+ years. Effective communication skills to drive effective reviews for his/her desk with Leadership. Demonstrate strong Sourcing and Negotiation skills to deliver YoY business results in Service, Cost, Cash & Vendor Performance. About Us We produce globally recognized brands, and we grow the best business leaders in the industry. With a portfolio of trusted brands as diverse as ours, it is paramount our leaders are able to lead with courage the vast array of brands, categories and functions. We serve consumers around the world with one of the strongest portfolios of trusted, quality, leadership brands, including Always®, Ariel®, Gillette®, Head & Shoulders®, Herbal Essences®, Oral-B®, Pampers®, Pantene®, Tampax® and more. Our community includes operations in approximately 70 countries worldwide. Visit http://www.pg.com to know more. We are an equal opportunity employer and value diversity at our company. We do not discriminate against individuals on the basis of race, color, gender, age, national origin, religion, sexual orientation, gender identity or expression, marital status, citizenship, disability, HIV/AIDS status, or any other legally protected factor. At P&G, the hiring journey is personalized every step of the way, thereby ensuring equal opportunities for all, with a strong foundation of Ethics & Corporate Responsibility guiding everything we do. All the available job opportunities are posted either on our website - pgcareers.com, or on our official social media pages, for the convenience of prospective candidates, and do not require them to pay any kind of fees towards their application.” Job Schedule Full time Job Number R000131711 Job Segmentation Experienced Professionals (Job Segmentation) Show more Show less

Business Unit: ESI HQ & Other Division: Legal - Business Challenge Yourself and Impact the Future! Element Solutions Inc (NYSE: ESI) is a leading specialty chemicals company whose operating businesses (see below) formulate a broad range of solutions that enhance the performance of products people use every day. Developed in multi-step technological processes, our innovative solutions enable our customers' manufacturing processes in several key segments, including electronic circuitry, communication infrastructure, automotive systems, industrial surface finishing, consumer packaging, and offshore energy. Customers of ESI’s businesses use our innovation as a competitive advantage, relying on ESI to help them navigate in fast-paced, high-growth markets. The breadth of ESI’s offerings provides strong strategic value to the end markets they serve. With over 5,500 people in operating facilities across more than 50 countries, ESI has established a growing legacy of creating technological advances for customers around the globe. Our people and technical sales teams are located close to our key markets, allowing us to maintain strong customer relationships and accelerate our product innovation process. Who are we looking for? We have an opportunity for a Regulatory Specialist to join the team and support the Product Regulatory department with customer surveys regarding regulations, internal queries regarding regulations, and supportive measures to put new products on the market. What will you be doing? Author product SDS that conform to global requirements Support secondary business with product regulatory needs Support customers with regulatory needs, such as SDS, regulation information, compliant products Investigate TSCA status of products and imported raw materials and complete all necessary paperwork to assure compliance Assist with preparation and review regulatory submissions for Government and State Agencies Assist with project work such as Asia analyses for specific regulations Who are You? Experience in chemical regulations in regions such as Asia, Europe, US. Knowledge in GHS, MSDS, SDS. Ability to handle customer surveys in a fast-paced environment. Possess a Bachelor's Degree in Chemistry or equivalent discipline. We understand that not all candidate may meet the requirements listed above. If you believe you have the skills and experience necessary to excel in this role, we encourage you to apply. What competencies will you need? Have the ability to work cross-functionally with a collaborative attitude. Ability to evaluate priorities and complete assigned tasks within timeframe. We are we Offering... As part of our team here, as well as receiving a competitive base salary, you will also participate in a generous performance related bonus scheme. In addition, you will also be covered under our corporate medical insurance plan and annual leaves. Teamwork At ESI, you will be part of a highly collaborative culture that promotes continuous improvement through cross-functional partnerships to achieve our mission. We do this through a strong and unified culture and transparent management which has empowered us to create high performing global teams that achieve superior solutions for our customers. Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Show more Show less

Job Opportunities for Structural Engineers (Remote Work - India) We are currently seeking talented Junior and Senior Structural Engineers and Steel Estimators with US project experience to join our team remotely in India. If you have a passion for structural design and want to work on innovative projects, we encourage you to apply! Position 1: Junior Structural Engineer Experience Required: 4-7 years Education: Master's Degree Structural Engineering Location: Remote (India) Key Skills & Requirements: Proficient in the design of steel, wood, concrete, masonry , and cold-formed structures Experience with ASCE 7 , AISC Steel Code , ACI , NDS , and other building codes Expertise in structural design software including Staad , Ram Element , Etabs , Bluebeam , Enercalc , and other relevant tools Proficient with steel structures and wood structures design Experience with design of main steel connections using AISC code required Expereince with design of misc metals such as stairs/railings/ladders required Strong written and verbal communication skills Ability to handle technical aspects of engineering work Proficient in computer literacy Position 2: Senior Structural Engineer Experience Required: 7-12 years Education: Master's Degree in Structural Engineering Location: Remote (India) Key Skills & Requirements: Expertise in steel, wood, concrete, masonry , and cold-formed structures design In-depth knowledge of ASCE 7 , AISC Steel Code , ACI , NDS , and other building codes Advanced proficiency in Staad , Ram Element , Etabs , Bluebeam , Enercalc , and other relevant software Proven leadership and project management skills High level of experience with design of main steel connections using AISC code required High level of expereince with design of misc metals such as stairs/railings/ladders required Ability to guide/mentor/delegate/review work of junior engineers Excellent written and verbal communication abilities Strong technical expertise and computer skills Highly Proficient with steel structures design and steel connection design is a plus Position 3: Estimator for Steel - Main steel connection design & Miscelleneous Metal design High level of Experience with reading structural and archtiectural drawings On Structural drawings -identifying/quantifying time required to perform main steel connection design for shear, moment, bracing and others that are NOT fully detailed on EOR drawings. ON Architectural drawings - identifying/quantifying all miscelleneous metal scope items such as stairs,railings, ladders, gates, sink support frames and other similar miscelleneous metal framing that requires delegated structural design. Steel detailing experience with Tekla and/or SDS software a plus Structural steel design experience with main steel connections and misc metals a plus What We Offer: Remote work opportunity from India, freelance/part-time TO Full-time Collaborative and growth-oriented work environment How to Apply: Please send your resume to apatel@mppengineers.com , including SAMPLE project drawings and hand calculations that you have personally worked on that demonstrates your knowledge of structural engineering per above specific requirements. Ensure to specify your years of experience and proficiency with the required tools. We look forward to welcoming you to our team of structural engineers! PLEASE DO NOT APPLY IF YOU DONT SATISFY ABOVE REQUIREMENTS. Show more Show less

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting, Office About Team: Antibody team The antibody team is involved in engineering and development of antibodies, with a deep focus on reagent quality and specificity. The core activities of the team include design, development, purification, conjugation, and testing of antibodies in a variety of immunoassay applications using groundbreaking tools and technologies. The goal of the program is advanced product development and creation of product-specific information to promote research use. Role: To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular, protein, biochemical, and cell biology methods. Responsibilities: Meticulous experimental planning and execution to meet program goals. Timely record keeping of results into data sheets and laboratory notebooks. Regular mining of literature and keeping oneself up to date with developments in the field. Compilation and presentation of data in written and oral formats. Active participation in team meetings with attention to detail and adherence to schedules. Strong theoretical and proven understanding of protein and antibody conjugation chemistries. Hands-on experience in performing protein or antibody conjugations to dyes, labels, or reporter tags. Experience with the development of new conjugation protocols and the design of site-specific conjugation strategies is desirable. Experience and knowledge in protein purification and analysis technologies such as affinity or ion exchange chromatography, SEC, HPLC, and SDS-PAGE. Experience or familiarity with antibody or protein engineering, rational design of mutants, and molecular biology. Experience with structural biology and protein modeling and visualization tools such as Pymol, Shrodinger, Discovery Studio or other similar programs is desirable. Theoretical or practical experience in antibody development platforms is desirable. Proficient in MS Office applications such as Word, PowerPoint, Excel, and possess a strong statistical knowledge and familiarity with statistical software such as Prism. Seeking self-motivated candidate who excels in learning and applying new concepts for process or product improvements. Must have strong interpersonal skills to connect with peers and leadership. Show more Show less

Looking for Surgery Coder Designation - Medical Coder & QCA Location - Bangalore Salary - open Discussion Immediate joiners or within 1 month Certified or Noncertified We can take. Interested call 9677147672

Hiring for Surgery Coder Designation - SR Coder / QCA Location: Bangalore / Chennai Exp : Coder : 1 to 3yrs / QCA : 4 to 6yrs Salary : Open to Discuss Immediate or 1 month notice Accepted Certified or Non Certified Contact Anushya HR 8122771407

Certified Medical Coder Experience - 1 to 5 yrs Salary - Based on Experience Immediate Joiners Preferred Specialty Needed : ENM IP / ED / Denials / Surgery Multispecialty / HCC Location - Bangalore / Hyderabad

Roles & Responsibilities : Program Management : Lead end-to-end program planning, execution, and delivery across multiple software and hardware teams. Define scope, timelines, budgets, resources, and success criteria in alignment with stakeholders. Track program status and KPIs, and provide regular updates to senior leadership and global customers. Manage risks, dependencies, and change control across parallel tracks and geographies. Technical Leadership : Partner with engineering and product leads to drive architecture, design, and technical implementation decisions. Review technical milestones and ensure adherence to Bosch quality gates and compliance standards. Support design reviews, code walkthroughs, and system integration planning when required. Stakeholder and Customer Engagement : Act as the primary point of contact for global customers and internal business units. Manage stakeholder expectations through clear communication and regular reporting. Ensure alignment across customer requirements, regulatory needs, and program deliverables.

We are looking for Experienced General Surgery Coders to join our growing team. The ideal candidate will have a strong background in surgical procedure coding across various specialties, including but not limited to general surgery, orthopedics, cardiovascular, and more. Role & responsibilities : Review and analyze medical records to assign appropriate CPT, ICD-10-CM, and HCPCS codes Ensure coding accuracy and compliance with official coding guidelines and payer requirements Work with clinical staff for clarifications and documentation improvement Maintain productivity and quality standards Preferred candidate profile Minimum 1 years of hands-on experience in surgical coding Certified Professional Coder (CPC) or Certified Coding Specialist (CCS) Attention to detail and excellent analytical skills Strong knowledge of anatomy, medical terminology, and surgical procedures Perks and Benefits Competitive salary with incentives Continuous training and career development Supportive work culture Complimentary meals provided To Apply: Send your resume to - amith.baswaraj@coronishealth.com For more details, contact us at 8971789084

Job Summary: We are currently looking for a skilled and safety-conscious Chemical Cleaning Technician to join our industrial services team. The ideal candidate will have hands-on experience in executing chemical cleaning procedures on heat exchangers, pipelines, boilers, and other industrial equipment. Knowledge of handling chemicals safely and operating cleaning systems is essential. Key Responsibilities: Perform chemical cleaning of industrial systems, equipment, and pipelines using approved procedures. Prepare and handle chemical solutions according to technical specifications and safety guidelines. Operate pumps, hoses, tanks, and other equipment involved in the chemical cleaning process. Assist in system flushing, passivation, and neutralization activities as required. Monitor cleaning progress and maintain accurate records of cleaning parameters and operations. Ensure all operations are conducted in compliance with company safety standards and environmental regulations. Coordinate with site supervisors and team members to ensure timely completion of tasks. Perform housekeeping and proper disposal of chemicals and waste as per company policy. Requirements: 2–3 years of relevant experience in industrial chemical cleaning. Strong understanding of industrial chemicals and their safe handling. Familiarity with chemical cleaning procedures, such as acid cleaning, alkaline cleaning, and degreasing. Ability to read and follow technical procedures and safety data sheets (SDS). Physically fit and capable of working in confined spaces and elevated areas. Willingness to work flexible hours, including nights, weekends, and during shutdowns or turnarounds. Preferred Qualifications: High school diploma or technical certificate in chemical, mechanical, or industrial discipline. Valid training or certification in chemical handling, confined space entry, and HAZMAT (if applicable). Experience in oil & gas, power plant, or industrial maintenance projects is a plus. Job Types: Full-time, Permanent, Contractual / Temporary, Freelance Contract length: 12 months Pay: ₹10,358.12 - ₹62,379.91 per month Benefits: Cell phone reimbursement Food provided Health insurance Life insurance Provident Fund Schedule: Day shift Night shift Ability to commute/relocate: Bilaspur, Chhattisgarh: Reliably commute or planning to relocate before starting work (Preferred) Experience: similar: 1 year (Preferred) similar work: 1 year (Preferred) Shift availability: Day Shift (Preferred) Night Shift (Preferred) Willingness to travel: 25% (Preferred) Work Location: In person

Greetings from Coronis Ajuba (Formerly known as MiraMed Ajuba) We are looking for Experienced certified Surgery & IPDRG Auditors medical coders to join us. Interested candidates please call us @ 91+ 8667765320 or mail to raghul.krishnasamy@coronishealth.com to book interview slot. SURGERY Coders ( 3 to 8 yrs ) * Certified coders only * Experience : 2+ yrs of experience in SDS is must * Location : Hyderabad / Chennai * Work from Office * Competitive Salary with Food and other Benefits. * Immediate Joiners preferred IPDRG Coders & Auditors ( 3 to 12 yrs ) * Experience : 1 to 10 years * Only for Certified coders * Location : Hyderabad / Chennai * Work from Office * Competitive Salary with Food and other Benefits. * Immediate Joiners preferred Attractive Salary for immediate joiners. Grab the opportunity and refer your friends Interested Candidates send you resume to the below WhatsApp Number or Reach me out on 8667765320 Regards, Raghul - 8667765320 Human Resources Coronis Ajuba

Greetings From Annexmed!! We have openings for surgery coders (Any Certification is Mandatory) Interview mode: Virtual Looking for immediate joiners!!! Minimum 1+ years of Medical Coding Experience. Proficient knowledge of medical terminology with excellent Coding skills. Surgery Coding Same Day Surgery General Surgery Location: Chennai (Perungudi) Shift Timing: Day Shift Interested candidates can share your resumes or Call to the below mentioned contact number. 8939611811 Hema HR

Looking for any Certified/Non-Certified Medical coder Radiology 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 Radiology CODER/SR.CODER/QA Anesthesia Coder/QA Surgery Coder/QA

Opportunities for Medical coders ! IPDRG Coder (50k Joining bonus) Location - Chennai, Hyderabad, Bangalore Salary - Up to 1L + Inc Mode: Virtual Interview Work from office only Surgery coder Location - Chn & Blr Salary - Up to 66k + inc Mode: Virtual interview Work from office onl y Refer you friends and family... Send updated resume - 9884747586 / HR Dwayne

#SponsoredJobEIL Job Description Company Overview EIL Global IT Solutions and Services Pvt Ltd is a leading IT services provider with a presence in the Asia Pacific and EMEA regions. Headquartered in Adelaide, Australia, we specialize in digital transformation through our comprehensive IT infrastructure solutions, professional and managed services, and cutting-edge technologies such as AIOPS and blockchain solutions. With a team size of 11-50 employees, we strive to enhance business performance for our clients across various sectors. The below requirement is for our prestigious client. Position Overview Business Analyst is responsible for evaluation of customer business problems and the development of solutions and working with the vendor to meet business requirements also ensuring the product backlog capturing and maturity. Ensuring the team and downstream stakeholders understand the impact of changes. Should be able to ensure his/her team produces data dictionary; and document and understand Business processes. The successful candidate will take responsibility for addressing and supporting the UK and European business projects for new and existing products and functionality initiatives across our systems. The role will encompass the full spectrum of business analyst activities through the full project life cycle. Relationship management skills for the various business contacts for the area will be important to ensure a superior service to our clients is maintained. Key Responsibilities Understand complex business issues and can understand the technical implications associated with business requirements. Writing User Stories and helping with solutions Leading Story walkthroughs and 3 Amigos sessions for the delivery teams Doing extensive data analysis and deriving business insights from data. Handle a demanding work environment and maintain a very high level of deliverable quality. Interact with all levels of the business community, seeking approval from all stakeholders of the projects. Must be able drive solution discussions and produce solution design documents. Define the scope of a business requirement, decide the approach, and produce the specification. Drive the analysis effort from start to end for a given area keeping various stakeholders in the loop and getting approvals/sign offs from them. Assess and ensure that the solution being delivered is fit for purpose. Obtaining agreement on business analysis deliverables and ensuring that they meet all the requirements of the business and tracking these across multiple systems groups. Working with business leads within the team to identify, define, and clarify the scope / issues in terms of complex business/systems requirements. Functionality co-ordination across multiple system projects delivering common, re-usable functionality using service-oriented patterns. Acting as a proxy customer with the development teams, facilitating open communication between the customer & development team Driving user acceptance criteria with the customer Co-ordinate with onshore-offshore UK/India business analysts. Work with onshore-offshore UK/India development teams Interact & work with third party partners and suppliers. Stay abreast of key emerging products / industry standards in the Business Analysis arena. Contribute to BA forum, lead process improvement initiatives. Worked on APIs and SOA (service-oriented architecture) based systems. Skills required Strong SQL query writing skills and be able to do in-depth data analysis. Writing API contracts in Swagger. Should have experience of dealing with multiple Stakeholders, covering different geographies. Should have working experience of APIs Experience of business process re-engineering, analysis, user requirement gathering, gap analysis Should have experience producing functional specifications documents (FSDs) Should have experience producing Solution Design Specifications by working closely with architects and developer community. Ability to progress the analysis and drive decisions to close open issue through discussions with multiple stakeholders. Must be strong in translating business requirements to technical resources (internal and external) in supporting the project. Delivery and results focused. Strong customer awareness & business focus Strong documentation skills of standard SDLC artefacts like SRA/SDS etc. Fair idea of Agile methodology, familiar with Stories – requirements artefact used in Agile. Excellent inter-personal, communication, documentation, facilitation & presentation skills Ideally have experience of e-Business, e-Commerce & Internet technologies, best practices & industry standards Ideally have experience of working with business modelling tools e.g. UML and CASE tools e.g. EA, Rational Rose Domain knowledge- Asset Management or Investment banking. Job Types: Full-time, Permanent Pay: From ₹600,000.00 per year Benefits: Health insurance Provident Fund Ability to commute/relocate: Gurgaon, Haryana: Reliably commute or planning to relocate before starting work (Required) Application Question(s): What is your current and expected CTC Experience: Business Analyst: 4 years (Required) Work Location: In person

Greetings from R1RCM Hiring for surgery coders looking for SDS, Gastroenterology surgery ,General surgery, Cardiopulmonary Surgery , Cardio surgery location-Chennai/HYD minimum 1 to7 years of experience CPC/CCS certification is mandatory regular shift- 8.30 am to 5.30pm interview mode- virtual mode Benefits: Free pickup and drop facility will be provided Medical Insurance will be provided Contact person Harrishma HR Contact mail - hpalaniappan@r1rcm.com/ 9677152997 If you are not interested, refer any of your friends who has the relevant experience

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