681 Sds Jobs - Page 12

About Us GVR Technolabs Pvt Ltd , an Information Technology services company with expertise in design, deployment and management of hardware and software applications and technology infrastructures. We offer services to improve our clients efficiency, strengthen partnerships, increase profitability, and improve business processes with quality and value in a secure environment. Designation: Electronics Engineer Qualification: B. Tech/BE in Electronics & Communication Location: Cochin (Kerala) No. of vacancies: 01 Experience required : 06 months 01 Year Roles and Responsibilities: Attend/resolve defects/faults observed in Systems Installation of RHEL OS, user management, network configuration, etc. Application softwares installation, System configuration as per installation procedure, Defect identification and defect resolution (DI/DR) of software issues and other maintenance related issues. Collection of data logs and any other logs (wire shark, RHEL logs) Assembly/De-assembly as per system documents or Computer based training (CBT)software Identification/Localization of hardware defects, resolution of defects as per hardware manuals Maintain logbook for all observed/reported problem and action taken to resolve the problem Skills Required: Experience in CMS system/Command and Control system/Embedded system IEE12207 SDLC, networking, server based hardware etc. Overview of embedded electronics, PCI, PMC based architecture and Processors, SBC Graphic boards, LAN switches, etc. Understanding of documents like Schematics Diagrams (SDs), BDs and wire list (WL) etc. Arithmetic skills and understanding of number system Ability to work on both hardware/software as per requirement Interested and suitable candidates can forward resume to [HIDDEN TEXT] or Whatsapp@ 6238128661

Knowledge Excellent domain expertise and process knowledge about RCM for Hospital facility/Physician. Understanding of Facility hospital verses Physician coding with indepth knowledge of the specialties - E&M-IP/OP. Knowledge of EM – IP/OP, APC for optimizing the reimbursement and element of UHDDS and guidelines, Level of service determination with emphasis on Physical Examination & Medical Decision Making in Documentation guidelines, hospital E&M coding - initial/subsequent visit Good knowledge of Human Anatomy, Physiology, Pathophysiology, Pharmacology, Diagnostic Studies, Conservative and Surgical Treatments. Understanding of Operative Reports and other report types with documentation requirements. Aware of consequences of risky practices like up-coding and down-coding, Fraud and abuse, inflated documentation, HIPAA and CLIA rules mandating claim transmission. Responsibilities Will be responsible for supervising and managing a team of 100+ QAs Create an inspiring team environment with an open communication culture Design QA capacity planning as per project requirement Delegate tasks and set deadlines Manage Quality of OP (ED/EM/SDS/ANC/OBV), ProFee Surgery & EM, and IP DRG projects Quality control as per client SLA Ensure effective implementation of organization’s Quality Management System Monitor team performance and report on metrics Performing random audit of auditor Perform RCA on audits observations. Identify knowledge gaps and develop an action plan with quality leads and operation managers Discover training needs and provide coaching to QAs Listen to team members’ feedback and resolve any issues or conflicts Recognize high performance and reward accomplishments Encourage creativity and business improvement ideas Suggest and organize team building activities Identify improvement opportunities and initiate action plans for improvement

Role & responsibilities Hiring For Medical Coders || Surgery, ENM with Surgery, Denials Multispeciality , Radiology , OBGYN , ENM OP/IP Coders, ED Facility || Work From Office Location :- Chennai , Hyderabad Work From Office Day Shift Specialties :- Surgery || Notice period:- 0 - 60 days || Hyderabad, Chennai || Upto 10 lpa ENM with Surgery || Notice period:- 0 - 60 days || Chennai , Noida || Upto 10 lpa Denials Multispeciality || Hyderabad, Chennai, Noida || Notice period:- 0 - 60 days || Upto 10 lpa Radiology Coder || Chennai, Bangalore || Need immediate joiners || Upto 7.5lpa ENM IP /OP || immediate joiners || Upto 50 k takehome OBGYN || Hyderabad || Upto 10 LPA ED Facility || Chennai, Noida, Hyderabad || Upto 8.5lpa || Immediate joiners Min 1+ year experience into the above Specialty is mandate Only Certified 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

Knovea Pharmaceutical Pvt. Ltd. is looking for talented professionals to join our Process Engineering (Instrumentation) team in Indore, MP. Designation: AM/DM/Manager No. of openings: 3 Experience: 8 years to 15 years Location: Indore, MP Industry: Pharmaceutical Manufacturing (Formulation injectable) Key Responsibilities: Review of equipment’s design qualification documents like PI&D, FS, DQ, SDS, HDS, IQ, OQ & drawings if applicable etc. and its approval if required. Process equipment instruments shall be verified as per PI&D and as per electrical drawings instruments commissioning shall be done if required FAT to be done for the process equipment’s if required. Support shall be given to installation & commissioning activities. To support qualification activities for the equipment’s like IQ, OQ & PQ All the process equipment and utilities equipment’s field instruments shall be identified by the team and schedule shall be prepared for calibration. Manage the instrumentation team for schedule calibration activities. Approve the calibration vendor for third party calibrations. Review of calibration certificates and its approval if required. Coordination with the vendors Spares indents, QMS elements like change control, deviations etc. to be initiated and its approvals. To attend Equipment maintenances like preventive maintenance, breakdown etc. Preparation of SOP’s and its approvals. If you’re passionate about engineering excellence and innovation, we’d love to hear from you!

MSDS Author On-site (Mohali)/Hybrid/Remote| Full-time | 5-10 Yrs Job Summary We're seeking an experienced MSDS Author to join our team. Responsibilities include preparing material safety data sheets assessing product compositions and hazards according to country/region (current profile includes EU, North America including USA and Canada, and China). We prefer candidates who are open to working from the office but also provide skilled individuals with the option for hybrid or fully remote arrangements. Key Responsibilities Independently assess product compositions or chemical formulations to applicable country regulations Research hazards and properties of components to make appropriate MSDS classification for global regulations Determine appropriate Hazard Assessments and MSDS phrases based on the assessment Directly interact with overseas clients to meet their author ing requirements Actively work with other team members to incorporate improvement projects Mentor junior author s in platform utilization and other system/tools Create and format MSDS documents utilizing client suggested MSDS author ing platform Review completed MSDS s Requirements Bachelor's degree in chemistry from a reputed university 5-10 years prior MSDS author ing experience with reputed service providers or MNC chemicals manufacturing companies Strong analytical and English communication skills (written and verbal) Strong understanding of regulations (CLP, OSHA, WHMIS, GHS, 49 CFR, 29 CFR, HazCom, ROHS, Inventories, TDG, etc.) Knowledge of prevalent MSDS author ing software platforms - SAP EH&S and/or MSDgen, WERCS, or similar; Knowledge of extended SDS for ECHA is a plus Understanding of active versus inactive ingredients with respect to physical form, volume, and hazards Preferred Qualifications Good knowledge of MS Office and MS Teams The capability to author all 16 sections of SDS Knowledge of chemical compounds, families, and pharmaceutical products Interested candidates can send resume at tanvir.k@idsil.com

Roles & Responsibilities : Power Up Your Career: Shape Global Marketing Strategies:?Contribute to the development of cutting-edge, integrated marketing programs designed to achieve ambitious business objectives across Bosch SDS's global markets. Influence the future of a renowned global brand and see your work make a tangible impact. Orchestrate Brand Campaigns:?Lead the planning and execution of impactful brand campaigns that elevate Bosch's image and reinforce its position as a leader in technology. Manage all aspects of the campaign lifecycle, from strategy development to performance measurement. Fuel the Sales Engine:?Plan and execute demand generation activities that deliver high-quality leads to the sales pipeline. Contribute directly to Bosch SDS's growth by generating tangible business results. Enhance deal conversion rates:?Collaborate with sales and business teams to nurture leads and maximize conversion rates. Create integrated campaign plans that accelerate the lead cycle and establish Bosch SDS as the preferred technology partner. Collaborate with World-Class Teams:?Partner with high-performing business units, delivery, and sales teams to craft localized campaigns that resonate with diverse target markets. Leverage the strength of a collaborative environment to drive brand awareness and market leadership. Uncover Buyer Insights:?Analyze market trends and buyer journeys to provide actionable insights that inform strategic marketing planning. Contribute to Bosch's understanding of the evolving market dynamics and help shape the future of the Bosch SDS brand experience. Qualifications Educational qualification: We're looking for a driven marketing professional with 5-7 years of experience who is passionate about marketing and technology. A Master's degree (preferably in Marketing) combined with a proven track record in developing and executing successful marketing campaigns is essential Experience : IT services marketing background helps definitely… Mandatory/requires Skills : good knowledge on digital marketing and operations Preferred Skills : Smart, capable, can take people along Additional Information Desired Skills: Experience working with global markets Strong understanding of B2B marketing

Category: Software Development/ Engineering Main location: India, Karnataka, Bangalore Position ID: J0425-1686 Employment Type: Full Time Position Description: Company Profile: Founded in 1976, CGI is among the largest independent IT and business consulting services firms in the world. With 94,000 consultants and professionals across the globe, CGI delivers an end-to-end portfolio of capabilities, from strategic IT and business consulting to systems integration, managed IT and business process services and intellectual property solutions. CGI works with clients through a local relationship model complemented by a global delivery network that helps clients digitally transform their organizations and accelerate results. CGI Fiscal 2024 reported revenue is CA$14.68 billion and CGI shares are listed on the TSX (GIB.A) and the NYSE (GIB). Learn more at cgi.com. Job Title: SDS author Position: Senior software engineer/ SDS Author Experience: 4-8 years Category: Software Development/ Engineering Shift: General/Rotational Main location: Hyderabad Bangalore, Chennai, Mumbai and pune Position ID: J0325-1532 Employment Type: Full Time Education Qualification: Any graduation or related field or higher with minimum 3 years of relevant experience. Position Description: We are looking for a meticulous SDS Author skilled in global chemical regulatory standards to author, review, and maintain Safety Data Sheets (SDS), labels, and other hazard communication documents using the CGI PS360 platform. The role demands a strong grasp of chemical classification, toxicological data interpretation, and regulatory compliance across multiple jurisdictions. Your future duties and responsibilities: Key Responsibilities Author, update, and maintain SDSs, labels, and hazard communication documents using CGI PS360. Ensure compliance with GHS, REACH, CLP, OSHA HCS, WHMIS, and other international chemical regulations. Interpret chemical and toxicological data to assign accurate hazard classifications and statements. Collaborate cross-functionally with regulatory, toxicology, and product teams for data verification and approval. Manage document version control and facilitate multi-language document generation and localization. Monitor and incorporate regulatory updates into SDS and labeling documentation. Required qualifications to be successful in this role: Qualifications Bachelor’s or Master’s degree in Chemistry, Toxicology, Environmental Science, or related discipline. Minimum of 1+ years experience in SDS authoring or chemical regulatory compliance. Strong knowledge of global SDS formats and regional chemical classification systems. Experience with CGI PS360 or similar SDS authoring tools such as The WERCS, Intelligent Authoring, MSDGen, SAP EHS. Familiarity with chemical databases like IUCLID and ChemIDplus. ________________________________________ Preferred Qualifications Certification in GHS/SDS authoring or Product Stewardship (e.g., AIHA SDS Author Certificate). Exposure to SAP EHS, REACH registration systems, or Poison Centre Notification tools. CGI is an equal opportunity employer. In addition, CGI is committed to providing accommodation for people with disabilities in accordance with provincial legislation. Please let us know if you require reasonable accommodation due to a disability during any aspect of the recruitment process and we will work with you to address your needs. Skills: Environmental Sciences Hazardous Materials Safety Safety Document Management English What you can expect from us: Together, as owners, let’s turn meaningful insights into action. Life at CGI is rooted in ownership, teamwork, respect and belonging. Here, you’ll reach your full potential because… You are invited to be an owner from day 1 as we work together to bring our Dream to life. That’s why we call ourselves CGI Partners rather than employees. We benefit from our collective success and actively shape our company’s strategy and direction. Your work creates value. You’ll develop innovative solutions and build relationships with teammates and clients while accessing global capabilities to scale your ideas, embrace new opportunities, and benefit from expansive industry and technology expertise. You’ll shape your career by joining a company built to grow and last. You’ll be supported by leaders who care about your health and well-being and provide you with opportunities to deepen your skills and broaden your horizons. Come join our team—one of the largest IT and business consulting services firms in the world.

Greetings from NTT DATA, In this Role you will be Responsible for: Should have experience in Radiology/E&M/ED/Surgery/IVR The coder reads the documentation to understand the patient's diagnoses assigned. Transforming of healthcare diagnosis, procedures, medical services, and equipment into universal medical alphanumeric codes Creating uniform vocabulary for describing the causes of injury, illness & death is the role of medical coders. Medical coding allows for Uniform documentation between medical facilities. The main task of a medical coders is to review clinical statements and assign standard Codes Requirements of the role include: 1 Year of experience in any Healthcare BPO - University degree or equivalent that required 3+ years of formal studies Ability to work scheduled shifts from Monday-Friday 7:30 AM to 5:30 PM IST and the shift timings can be changed as per client requirements. It is Mandatory to return to office based on client or business requirement. We dont have any openings for HCC only for E/M , ED, Surgery, Radiology and IVR. Interested Candidate Please share me your Resume to Ganga.Venkatasamy@nttdata.com

Dear ED Pro & Facility Coder's Greetings from Access healthcare (No freshers) CERTIFICATION IS MANDATORY. Minimum 1 year experience needed Salary as per market standards Only for certified coders Relieving letter is not mandatory Immediate joiner have to join by the same week About the Role: We are seeking skilled and detail-oriented Ed Medical Coders to join our growing team. If you have a passion for accuracy, compliance, and education in the healthcare domain, this is your opportunity to make a meaningful impact. Interview Mode: Virtual Location: Chennai Contact : HR SAMEEMA - 7339689430 (Interested please share your resume to mentioned number)

Job Description Hiring For IVR, ENM, Denial, surgery, IPDRG,ED coder || upto 12lpa || CODERS : Surgery Coder : Chennai / Hyderabad / Bangalore || upto 75k Take home || IPDRG Coder : Hyd / Chennai / Bangalore || CTc upto 13 LPA || Denial coder : Hyderabad / Chennai || upto 75k Take home || IVR coder : HYDERABAD || upto 75k Take home || ENM Coder : Chennai || upto 7.5 lap Experience : Minimum 1 year relevant experience is mandatory Work from office Freshers are not Eligible Interested candidates can share your updated resume at 9603760528 prananya.axisservices@gmail.com Refer your friend's / Colleagues Axis Services Preferred candidate profile min 1yr exp into Medical coder Perks and Benefits week 5 Days

PROCESS COACH Job Description: Understand the quality requirements both from process perspective and for targets. To Train effectively the new joiners on Medical Coding concept with the guidelines. To monitor Trainees productivity and quality output per OJT glide path/ramp up targets. Providing continuous feedback in a structured manner. Educating on the client specs and guidelines. Educating on the latest updates on the coding aspects. Carrying out one-on-one session on the repeated errors. To provide feedback on productivity and quality of trainees to Team Leads. To pass on the QC feedback effectively to the trainees. To help Team Leads in early confirmation of Trainees by providing the valuable inputs. Job Specification: Minimum of 3 Years of Professional and Relevant Experience in Medical Coding with specialty surgery. Extensive Coaching & Trainingas per process defined. Must have Variant Training & Coaching Strategy. Must have Coding Certification like CPC, CCS, COC, AHIMA. Any graduate will do. Shift Details: General Shift / Day Shift Work Mode: WFO

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

Surgery Coding openings at Advantum Health Pvt Ltd, Hyderabad. Should have at least 4plus years experience in Surgery Coding Show have valid coding certification Dayshift and Work from office Walk-in for interview between 2pm to 5pm on Mondays and Wednesdays. For non local, virtual interview is available Ph:9177078628, 8247410763, 9059683624, #Address: Advantum Health Private Limited, Cyber gateway, Block C, 4th floor Hitech City, Hyderabad. Location: https://www.google.com/maps/dir//Advantum+Health+India,+CYBER+GATEWAY,+4th+Floor,+Block+C+Wing+2,+Phase+2,+HITEC+City,+Hyderabad,+Telangana+500081/data=!4m6!4m5!1m1!4e2!1m2!1m1!1s0x3bcb930059ea66d1:0x5f2dcd85862cf8be?sa=X&ved=1t:57443&ictx=111 Follow us on LinkedIn, Facebook, Instagram Advantum Health LinkedIn Page: https://www.linkedin.com/showcase/advantum-health-india Advantum Health Facebook Page: https://www.facebook.com/profile.php?id=61564435551477 Advantum Health Instagram Page: https://www.instagram.com/reel/DA8hHRWOIyW/?igsh=MXN6dXoxcXAwYjF0MQ==

HIRING MEDICAL CODERS || ENM with surgery , ENM op , SDS coder || Hyderabad , Chennai || Eligibility Criteria : Enm with Surgery : Min 1 yr of exp into enm with surgery coding || Chennai , Noida || 10 lpa Sds coder : Min 1 yr of exp into sds coding || Hyderabad , Chennai and Noida || 10 lpa Denials coder : Min 1 yr of exp into Denials coding || Hyderabad , Chennai and Noida || 10 lpa work from office only Hyderabad, Chennai, Noida Relieving letter is mandatory Interested candidates can share their resumes to HR Ramadevi: 7842224022 EMAIL : ramadevi.axisservices@gmail.com

Hiring for Medical Coders || Up to 9 LPA || Locations : Hyderabad , Chennai , Noida || Min 1 + yr of exp in below mentioned specialisation's Ed facility - Hyderabad , Chennai (Only Immediate joiners) OBGYN , IVR - Hyderabad Surgery - Hyderabad , Chennai , Noida EM with Surgery - Chennai Denials multi-speciality - Hyderabad , Chennai Only Certified Coders Up to 9 LPA Notice Period : 0-60 Days Relieving letter is mandatory Interested candidates send Your Resume To: Email: lalithahr.axis@gmail.com WhatsApp: HR Lalitha - 8179142981

Dear Coder's, Greetings from Access healthcare Massive hiring for Experienced & Certified Coders/QA, (No freshers) CERTIFICATION IS MANDATORY. Minimum 1 year experience needed Salary as per market standards Only for certified coders Relieving letter is not mandatory Preferably Immediate - 10-15 days' notice period acceptable, Required Specialty : Denial - Chennai, Coimbatore, Pune E/M OP Coder - Chennai, Coimbatore, E/M OP TO DENIAL- Coder - Chennai, Coimbatore Surgery - Chennai, Coimbatore, Pune ED Facility - Chennai, Coimbatore, Pune Interview Mode: Virtual. Work mode: WFO/WFH both available. Contact : HR kowsalya - 8122343331 (Interested please share your resume to mentioned number) Refer and share with someone who might be a great fit! Regards, HR kowsalya Recruiter Talent Acquisition | Access HealthCare Ph: 8122343331 Email: kowsalya.k@accesshealthcare.com web: www.accesshealthcare.com

Identify appropriate assignment of ICD - 10 - CM and ICD - 10 - PCS Codes for inpatient services provided in a hospital setting and understand their impact on the DRG with reference to CC / MCC, while adhering to the official coding guidelines and established client coding guidelines of the assigned facility Abstract additional data elements during the Chart Review process when coding, as needed Adhere to the ethical standards of coding as established by AAPC and / or AHIMA Ability to code 1.5-2.5 charts per hour and meeting the standards for quality criteria Needs to constantly track and implement all the updates of AHA guidelines Provide documentation feedback to providers and query physicians when appropriate Maintain up - to - date Coding knowledge by reviewing materials disseminated / recommended by the QM Manager, Coding Operations Managers, and Director of Coding / Quality Management, etc. Participate in coding department meetings and educational events Review and maintain a record of charts coded, held, and / or missing Be an ideal team player who can work in a large group and provide inputs to the team for betterment of the team in terms of quality and productivity Under general supervision, organizes and prioritizes all work to ensure that records are coded and edits are resolved in a timeframe that will assure compliance with regulatory and client guidelines Adherence with confidentiality and maintains security of systems. Compliance with HIPAA policies and procedures for confidentiality of all patient records Demonstrates knowledge of security of systems and associated policies and procedures for maintaining the security of the data contained within the systems Comply with the terms and conditions of the employment contract, company policies and procedures, and any and all directives (such as, but not limited to, transfer and/or re-assignment to different work locations, change in teams and/or work shifts, policies in regards to flexibility of work benefits and/or work environment, alternative work arrangements, and other decisions that may arise due to the changing business environment). The Company may adopt, vary or rescind these policies and directives in its absolute discretion and without any limitation (implied or otherwise) on its ability to do so Life Science or Allied Medicine Graduates Certification from AAPC or AHIMA (CIC certification preferred) 5+ years of Acute Care Inpatient medical coding experience (hospital, facility, etc.) Experience with working in a level I trauma center and / OR teaching hospital with a mastery of complex procedures, major trauma ER encounters, cardiac catheterization, interventional radiology, orthopedic and neurology cases, and observation coding ICD - 10 (CM & PCS) and DRG coding experience

Location: Bengaluru, KA, IN Company: ExxonMobil About us At ExxonMobil, our vision is to lead in energy innovations that advance modern living and a net-zero future. As one of the world’s largest publicly traded energy and chemical companies, we are powered by a unique and diverse workforce fueled by the pride in what we do and what we stand for. The success of our Upstream, Product Solutions and Low Carbon Solutions businesses is the result of the talent, curiosity and drive of our people. They bring solutions every day to optimize our strategy in energy, chemicals, lubricants and lower-emissions technologies. We invite you to bring your ideas to ExxonMobil to help create sustainable solutions that improve quality of life and meet society’s evolving needs. Learn more about our What and our Why and how we can work together . ExxonMobil’s affiliates in India ExxonMobil’s affiliates have offices in India in Bengaluru, Mumbai and the National Capital Region. ExxonMobil’s affiliates in India supporting the Product Solutions business engage in the marketing, sales and distribution of performance as well as specialty products across chemicals and lubricants businesses. The India planning teams are also embedded with global business units for business planning and analytics. ExxonMobil’s LNG affiliate in India supporting the upstream business provides consultant services for other ExxonMobil upstream affiliates and conducts LNG market-development activities. The Global Business Center - Technology Center provides a range of technical and business support services for ExxonMobil’s operations around the globe. ExxonMobil strives to make a positive contribution to the communities where we operate, and its affiliates support a range of education, health and community-building programs in India. Read more about our Corporate Responsibility Framework. To know more about ExxonMobil in India, visit ExxonMobil India and the Energy Factor India. What role you will play in our team The PE/PP Regulatory business compliance Advisor is responsible for engaging with EMPS Sales and Marketing & Technology functions to assess and develop Safety Data Sheets (SDS), Product Regulatory Statements, & related Chemical Management information to support our customers and maintain compliance across the markets and segments we operate. The support provides our employees and customers in the safe cradle-to grave handling of our products as well as compliance with the Corporate Product Safety Policy and regulations in the countries in which we do business. In addition, the BCA provides insight to the rapidly evolving regulatory frameworks to the business lines to inform product design and marketing strategies. Job location is based out of Bangalore, Karnataka What you will do Review product composition and regulatory information to finalize SDSs of PE and PP products Work as subject matter expert to advise regulatory compliance statements required by internal and external customers to support sensitive end use applications (SEUS) Registration, volume tracking and compliance management of substances registered under REACH and REACH-like regulations (K- REACH,EU, UK, KKDIK) Provide REACH OR services to respective business. Develop, lead, and execute REAH related projects. Monitoring and product regulatory determination w.r.t. specific regulations, e.g. ROHS, IMDS, IEC, GADSL regulations. Assess regulatory compliance impact due to proposed changes with material/supplier/formulation and recommend compliance actions. Develops and informs business of product design choices to positively position finished product in the evolving regulatory framework inclusive of sustainability initiatives/targets About you Skills and Qualifications Bachelor or Master degree in science from a recognized university with minimum GPA 7.0 Chemical or petroleum industry Product Stewardship Compliance experience strongly preferred REACH dossier development, submission and compliance experience preferred Deep expertise in product and chemical regulations across EMEA (European, UK, Turkey) and APAC (South Korea, etc.) Petrochemical laboratory, quality control, manufacturing experience preferred Familiarity with regulations for Chemical Classification and Labelling (GHS/CLP) and Product Transportation Classification Excellent communication skills Technical proficiency (SAP, Salesforce and IUCLID) Your benefits An ExxonMobil career is one designed to last. Our commitment to you runs deep: our employees grow personally and professionally, with benefits built on our core categories of health, security, finance and life. We offer you: Competitive compensation Medical plans, maternity leave and benefits, life, accidental death and dismemberment benefits Retirement benefits Global networking & cross-functional opportunities Annual vacations & holidays Day care assistance program Training and development program Tuition assistance program Workplace flexibility policy Relocation program Transportation facility Please note benefits may change from time to time without notice, subject to applicable laws. The benefits programs are based on the Company’s eligibility guidelines. Stay connected with us Learn more about ExxonMobil in India, visit ExxonMobil India and Energy Factor India. Follow us on LinkedIn and Instagram Like us on Facebook Subscribe our channel at YouTube EEO Statement ExxonMobil is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin or disability status. Business solicitation and recruiting scams ExxonMobil does not use recruiting or placement agencies that charge candidates an advance fee of any kind (e.g., placement fees, immigration processing fees, etc.). Follow the LINK to understand more about recruitment scams in the name of ExxonMobil. Nothing herein is intended to override the corporate separateness of local entities. Working relationships discussed herein do not necessarily represent a reporting connection, but may reflect a functional guidance, stewardship, or service relationship. Exxon Mobil Corporation has numerous affiliates, many with names that include ExxonMobil, Exxon, Esso and Mobil. For convenience and simplicity, those terms and terms like corporation, company, our, we and its are sometimes used as abbreviated references to specific affiliates or affiliate groups. Abbreviated references describing global or regional operational organizations and global or regional business lines are also sometimes used for convenience and simplicity. Similarly, ExxonMobil has business relationships with thousands of customers, suppliers, governments, and others. For convenience and simplicity, words like venture, joint venture, partnership, co-venturer, and partner are used to indicate business relationships involving common activities and interests, and those words may not indicate precise legal relationships. Job Segment: Sustainability, Chemical Research, CSR, ERP, SAP, Energy, Engineering, Management, Technology

Job Description Hiring For IVR, ENM, Denial, surgery, IPDRG,ED coder || upto 12lpa || CODERS : Surgery Coder : Chennai / Hyderabad / Bangalore || upto 75k Take home || IPDRG Coder : Hyd / Chennai / Bangalore || CTc upto 13 LPA || Denial coder : Hyderabad / Chennai || upto 75k Take home || IVR coder : HYDERABAD || upto 75k Take home || ENM Coder : Chennai || upto 7.5 lap Experience : Minimum 1 year relevant experience is mandatory Work from office / Relieving is mandatory Freshers are not Eligible Interested candidates can share your updated resume at 9030874428 Refer your friend's / Colleagues Axis Services Preferred candidate profile min 1yr exp into Medical coder Perks and Benefits week 5 Days

Job Description: Meet all Client Service Level Agreements (deliverables) Ensure the team understands client specific training requirements / needs etc. Analyse performance results of the team and implement process improvements. Determine appropriate staff levels and implement strategies to ensure efficient operations. Work with support departments to ensure staffing strategies are effectively executed. Hold team meetings on a regular basis with direct reports. Communicate all process and client updates to direct reports within specific timelines and keep record for such updates. Act as single point contact for the Team Leaders for all their client and team members related needs and create a harmonious work environment. Responsible for day-to-day functional supervision of each team, including productivity of the team, quality %, track absenteeism of the team and encourage team managers to complete performance appraisal of work group(s) in accordance with the organizations policies and applicable legal requirements. Job Specification: Minimum of 10 Years of Professional and Relevant Experience in Medical Coding Must have experience in Client and Stakeholder and Quality Management. Excellent experience in Team and People Management as well. Must have Coding Certification like CPC/ CCS/ COC/ AHIMA + Quality Any graduate will do. Shift Details :General Shift / Day Shift Work Mode :WFO

Job Title: Molecular Biologist – qPCR Consultant (Preclinical – In Vitro) Location: MS Clinical Research Pvt Ltd (MSCR) Department: Preclinical – In Vitro Employment Type: Consultant/ Part- time Experience: Minimum 10 years in Molecular Biology with hands-on expertise in qPCR Role Overview: MSCR is seeking an accomplished Molecular Biologist – qPCR Consultant to support our preclinical (in-vitro) research team. The ideal candidate will bring deep technical expertise in qPCR assay development, optimization, and data analysis, specifically aligned with preclinical drug screening and mechanistic in-vitro studies. This is a strategic consulting role aimed at enhancing our molecular biology capabilities in gene expression, target validation, and biomarker discovery. Key Responsibilities: Provide technical leadership in the design, development, and validation of qPCR assays for in-vitro studies including cytotoxicity, gene expression profiling, and pathway analysis. Advise on sample preparation, RNA/DNA extraction, and quality control specific to in-vitro systems (e.g., cell lines, primary cultures). Guide the team in primer/probe design, assay optimization (SYBR/TaqMan), and standard curve generation. Troubleshoot experimental issues and recommend improvements to protocols and workflows. Ensure robust data integrity, statistical soundness, and scientific documentation of qPCR results. Review experimental designs to align with regulatory and scientific requirements for GLP-compliant preclinical studies. Train lab scientists on best practices for qPCR technique and data interpretation. Collaborate with research scientists and study directors to integrate molecular endpoints in preclinical study design. Stay updated with emerging trends, technologies, and best practices in molecular biology and qPCR. Qualifications: Ph.D. or Master’s in Molecular Biology, Cell Biology, Biotechnology, or a related field. Minimum 10 years of hands-on experience in molecular biology techniques, with a strong focus on qPCR in in-vitro preclinical models. Excellent analytical, documentation, and communication skills. Desirable Skills: Knowledge of cell-based assay systems, molecular endpoints, and biomarker quantification. Exposure to RT-qPCR, miRNA analysis, or multiplex PCR. Understanding of statistical software or qPCR analysis tools (e.g., SDS, CFX Maestro, Bio-Rad CFX, REST). Engagement Type & Compensation: Consulting basis – Part-time, Remote, Hybrid Remuneration commensurate with experience and scope of involvement.

Medical coding SDS Chennai & Hyderabad Roles and Responsibilities: - Accurately code SDS and Special Procedures through review of medical record documentation and encounter forms for Outpatient facility Utilize EPIC and 3M systems for SDS/OBS/Special Procedure coding. 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) Should have good knowledge in Cardiac catheterization with 9xxxx series codes. Desired Candidate Profile: - Should be a Science Graduate. Minimum of 1+ years of experience in SDS. 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. For More Information: Contact : Sandhiya - 7550106180 or sandhiya.haridass@sutherlandglobal.com Note: "Sutherland never requests payment or favors in exchange for job opportunities. Please report suspicious activity immediately to TAHelpdesk@Sutherlandglobal.com "

Overview: The primary job function of the Field Application Specialist includes but not limited to: Provide pre and post sales technical application support to customers to achieve customer satisfaction and business objectives. Conduct product application trainings to customers and to internal team members. Manage product evaluation at customer site to meet business objectives Support sales personnel to achieve team objectives He/she needs to be independent, self-motivated, likes to work with different people and can work under pressure. He should be ready for frequent traveling as almost 75% traveling is required in this position. Possess positive attitude towards work, forthcoming, ability to multi-task, creative in handling technical application service matters/problems. He/she should possess exceptional verbal and written communication skills, excellent inter-personal skill, soft skill in customer relation management, organization skill, as well as excellent technical analysis and problem-solving skills. How You’ll Make an Impact: Provide pre- and post-sales technical application support Provide post-sales technical application support & training mainly for trouble shooting purpose to achieve customer satisfaction and meet business objectives Develop a systematic troubleshooting approach to diagnose common application problems to be shared among team members. Manage product evaluation and provide feedback on further evaluation needs at customer site as part of sales process and ensure it meets business objectives Conduct pre-sales product presentations and demonstrations. Create training / Demo module (training notes, equipment, consumables & checklist) to be used as reference for other FAS. Work with manager to devise the yearly application training plan Ensure that the Bio-Rad commitment to customer satisfaction is achieved and constantly improved. Log in all field visits in Salesforce (SFDC) and upload supporting reports Maintain internal documents for application trainings conducted Ensure all instruments used for evaluation are properly accounted for Collect reference/performance letters for different products from customers regularly Presentation on specific product applications Prepare materials required for workshop/exhibitions & seminars Manage relationships with key customers & develop reference/key seminars Managing products performance related complaints and replacement requests Submit product related complaints to Product team in timely fashion and do the evaluation Ensure that all relevant documentation is in order and traceable What You Bring: Experience of working in life science research laboratory for at least 2 years. Proactive and passionate to provide excellent support to meet customer satisfaction. Excellent written, oral communication and presentation skills. Must have proven track record of hands-on experience in conducting wet lab experiments for at least 2 of the techniques (preferably more) Protein Purification (FPLC) Chromatography SDS-PAGE, Western Blotting, Imaging (Protein/DNA gel & blot documentation) PCR, Electrophoresis, Real-Time PCR, Transfection Droplet Digital PCR (ddPCR) Flow cytometry, cell Imaging & cell culture ELISA, Multiplex Immunoassays and use of different antibodies Experience at managing evaluation and training Proven track record to meet customer satisfaction in a technical support environment Able to work independently and pro-actively Preferably Ph.D. in Life Sciences (Biotechnology, Biochemistry, Microbiology etc Minimum 2 years working experience in a life science research laboratory with strong technical understanding of laboratory procedures Superior technical application knowledge of diagnostic/research methodologies Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Recently voted a Best Place to Work, Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see. Benefits: Bio-Rad's biggest asset is its people, and the reason why our Total Rewards deliver programs that provide value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Our robust offerings serve to enrich the overall health, wealth, and wellbeing of our employees through the various stages of an employee’s work and life cycle. We’re proud to offer a variety of options, including competitive insurance plans for you and your immediate family, Annual Health checkup , Marriage Leave, Paternity Leave ,Employee Assistance Programme , extensive learning and development opportunities, and more. EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with disabilities, and people of all races, ethnicities, genders, ages, and orientations are encouraged to apply. Agency Non-Solicitation: Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resum

Choosing Capgemini means choosing a company where you will be empowered to shape your career in the way you’d like, where you’ll be supported and inspired by a collaborative community of colleagues around the world, and where you’ll be able to reimagine what’s possible. Join us and help the world’s leading organizations unlock the value of technology and build a more sustainable, more inclusive world. Your Role As an SAP EHS Consultant, you will be responsible for designing, implementing, and supporting SAP solutions that help organizations manage their environmental, health, and safety compliance effectively. You will work closely with business stakeholders to understand regulatory requirements and operational risks, and translate them into robust SAP EHS configurations and processes. Your role will involve end-to-end project involvement—from requirement gathering and blueprinting to configuration, testing, training, and post-go-live support. You will ensure that the SAP EHS module is aligned with global compliance standards and integrated seamlessly with other SAP modules such as MM, PM, and QM. Your expertise will contribute to creating safer workplaces, reducing environmental impact, and ensuring legal compliance across operations. Your Responsibilites Analyze business and regulatory requirements related to EHS and translate them into SAP EHS solutions. Configure and implement SAP EHS modules such as Product Safety, Dangerous Goods Management, Industrial Hygiene and Safety, Occupational Health, and Waste Management. Develop and maintain safety data sheets (SDS), labels, and compliance documentation. Integrate SAP EHS with other SAP modules (MM, PM, QM, etc.) and external systems. Support data migration, testing, user training, and go-live activities. Ensure compliance with global and local environmental, health, and safety regulations. Provide ongoing support, enhancements, and troubleshooting for SAP EHS processes. Collaborate with cross-functional teams to drive continuous improvement in EHS practices. Stay updated with SAP innovations and regulatory changes impacting EHS. Strong hands-on experience in SAP EHS configuration and implementation. In-depth knowledge of EHS regulatory requirements and compliance standards. Experience with SDS authoring, dangerous goods classification, and risk assessments. Familiarity with integration points between SAP EHS and other SAP modules. Excellent analytical, communication, and stakeholder engagement skills. SAP S/4HANA experience is a plus. Capgemini is a global business and technology transformation partner, helping organizations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end-to-end services and solutions leveraging strengths from strategy and design to engineering, all fueled by its market leading capabilities in AI, generative AI, cloud and data, combined with its deep industry expertise and partner ecosystem.

The primary job function of the Field Application Specialist includes but not limited to: Provide pre and post sales technical application support to customers to achieve customer satisfaction and business objectives. Conduct product application trainings to customers and to internal team members. Manage product evaluation at customer site to meet business objectives Support sales personnel to achieve team objectives He/she needs to be independent, self-motivated, likes to work with different people and can work under pressure. He should be ready for frequent traveling as almost 75% traveling is required in this position. Possess positive attitude towards work, forthcoming, ability to multi-task, creative in handling technical application service matters/problems. He/she should possess exceptional verbal and written communication skills, excellent inter-personal skill, soft skill in customer relation management, organization skill, as well as excellent technical analysis and problem-solving skills. How You’ll Make An Impact Provide pre- and post-sales technical application support Provide post-sales technical application support & training mainly for trouble shooting purpose to achieve customer satisfaction and meet business objectives Develop a systematic troubleshooting approach to diagnose common application problems to be shared among team members. Manage product evaluation and provide feedback on further evaluation needs at customer site as part of sales process and ensure it meets business objectives Conduct pre-sales product presentations and demonstrations. Create training / Demo module (training notes, equipment, consumables & checklist) to be used as reference for other FAS. Work with manager to devise the yearly application training plan Ensure that the Bio-Rad commitment to customer satisfaction is achieved and constantly improved. Log in all field visits in Salesforce (SFDC) and upload supporting reports Maintain internal documents for application trainings conducted Ensure all instruments used for evaluation are properly accounted for Collect reference/performance letters for different products from customers regularly Presentation on specific product applications Prepare materials required for workshop/exhibitions & seminars Manage relationships with key customers & develop reference/key seminars Managing products performance related complaints and replacement requests Submit product related complaints to Product team in timely fashion and do the evaluation Ensure that all relevant documentation is in order and traceable What You Bring Experience of working in life science research laboratory for at least 2 years. Proactive and passionate to provide excellent support to meet customer satisfaction. Excellent written, oral communication and presentation skills. Must have proven track record of hands-on experience in conducting wet lab experiments for at least 2 of the techniques (preferably more) Protein Purification (FPLC) Chromatography SDS-PAGE, Western Blotting, Imaging (Protein/DNA gel & blot documentation) PCR, Electrophoresis, Real-Time PCR, Transfection Droplet Digital PCR (ddPCR) Flow cytometry, cell Imaging & cell culture ELISA, Multiplex Immunoassays and use of different antibodies Experience at managing evaluation and training Proven track record to meet customer satisfaction in a technical support environment Able to work independently and pro-actively Preferably Ph.D. in Life Sciences (Biotechnology, Biochemistry, Microbiology etc Minimum 2 years working experience in a life science research laboratory with strong technical understanding of laboratory procedures Superior technical application knowledge of diagnostic/research methodologies Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Recently voted a Best Place to Work, Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see. Benefits: Bio-Rad's biggest asset is its people, and the reason why our Total Rewards deliver programs that provide value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Our robust offerings serve to enrich the overall health, wealth, and wellbeing of our employees through the various stages of an employee’s work and life cycle. We’re proud to offer a variety of options, including competitive insurance plans for you and your immediate family, Annual Health checkup , Marriage Leave, Paternity Leave ,Employee Assistance Programme , extensive learning and development opportunities, and more. EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with disabilities, and people of all races, ethnicities, genders, ages, and orientations are encouraged to apply. Agency Non-Solicitation: Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resum Legal Entity: (IND_3006)Bio-Rad Laboratories (India) Pvt Ltd