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Greetings from Starworth Global Solutions!! Surgery : Coder / QCA - Coding Loc : Bangalore ED Profee : Coder Loc : Bangalore E/M - IP : QCA Coding Des: QCA Coding Loc: Bangalore Interested Do share CV: Geetha S 9344502340

Hiring For Medical Coders || Surgery, ENM with Denials, ENM with Surgery, Denials Multispeciality , ENM OP/IP Coders || Work From Office Role & responsibilities Location :- Chennai , Hyderabad Work From Office Specialties :- Surgery || Notice period:- 0 - 60 days || Hyderabad, Chennai, Noida || Upto 10 lpa ENM with Surgery || Notice period:- 0 - 60 days || Chennai || Upto 10 lpa ENM with Denials || Notice period:- 0 - 60 days || Chennai , Noida || Upto 10 lpa Denials Multispeciality || Notice period:- 0 - 60 days || Chennai || Upto 10 lpa ENM IP or OP || Notice period:- 0 - 15 days || Chennai, Bangalore || Upto 50 k takehome || Releiving letter not mandate Clinical Documentation || Hyderabad location || Notice period:- 0 - 15 days || Upto 7.5lpa Only Certified Min 1+ year of experience into the above Specialties is mandate Last Company Relieving letter mandate 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 5 days working 2 way cab facility

Hiring Surgery Coder & QCA Exp: 1 to 5 yrs Salary : 55 K based on skills Location : Chennai & Bangalore Online Interview Work from office Skills : Min 1 yr experience in Surgery Coder Interested Call / Whatsapp your CV : 9344402033 Keerthi Required Candidate profile Required Candidate profile # Notice Period : upto 15 days # Relieving letter is not mandatory # Certified # Ready to relocate Bangalore # Day Shift Refer your Frnz

Hiring for Surgery Coders/Qca Any Certified coders Experience 1 years to 5 years Location Chennai All documents with UAN and PF account mandatory Immediate joiners only Share your updated CV to Sathiya HR 9677147672

EM IP OP Minor surgery / SDS / Surgery / OBGYN / IPDRG. Job description Hiring for Medical Coders || Up to 10 LPA || Locations : Hyderabad , Chennai , Bangalore , Noida || Min 1 + yr of exp in below mentioned specialization's ED facility - ED Profee - OBGYN , IVR (Interventional Radiology) Radiology - Chennai Surgery Coder EM OP , IP EM with Minor / Major Surgery Denials multispecialty IPDRG Coder Any Certification is fine (CPC , CCS , CIC , COC) Up to 10 LPA Notice Period : 30 days Relieving letter is mandatory Interested & Eligible candidates can share your updated resume to HR Poornima - 8098305966 (Watsapp)

Hiring for Ipdrg Coder/ sn coder and QA, For Coders - Minimum 1 year is required For QCA - Minimum 3 years is required. Successful completion of CPC or CCS certification, must be active during joining and verified. Location- Chennai US shifts Work from Office salary Negotiable Roles and Responsibilities: - Accurately code SDS and Special Procedures through review of medical record documentation and encounter forms for Outpatient facility General surgery and SDS QA and coder vacancy Hands on experience in coding tools such as EPIC, 3M, Optum. Assign CPT procedure codes, ICD-10 diagnosis codes, and modifiers based on documentation, government teaching physician documentation requirements and LCD/NCD/ NCCI policies. Should have working experience in all Surgery procedures (10000-69990 CPT series) Good knowledge in Cardiac catheterization with 9xxxx series codes is an added advantage. Minimum of 1 yr of experience Basic knowledge of medical terminology and anatomy. Comfortable to work from office. Effective verbal and written communication skills (Should have capability to reply properly to client and stakeholders. Successful completion of CPC or CCS certification must be active during joining and verified. Able to work independently and willing to adapt and change as per business/ process requirements. Please call varsha 7200847046 for more Info Regards varsha 7200847046

We are hiring experienced Medical Coders - IPDRG / General Surgery / Same-Day Surgery and Same Day Surgery with Evaluation and Management (E/M) Notice Period - 15 to 30 Days Preferred Job Description : We are actively hiring experienced medical coders across the following specialties: IPDRG (Certified / Non Certified ) Same-Day Surgery (SDS) Same Day Surgery (SDS) with Evaluation & Management (E/M) General Surgery Key Responsibilities: Review medical charts, surgical reports, and physician documentation Assign accurate ICD-10-CM, CPT, and HCPCS codes Ensure compliance with client-specific and CMS guidelines Maintain high accuracy and productivity Work with QA and auditing teams as needed Requirements: Minimum 1 to 2 years of experience in any of the mentioned specialties Certified Coders: CPC / COC / CCS (AAPC or AHIMA) Knowledge of modifiers, global periods, E/M leveling, and surgical coding Strong understanding of anatomy, physiology, and medical terminology Experience using tools like 3M, EncoderPro, or similar preferred What We Offer: Competitive Salary + Monthly Incentives CEU Support + Career Growth (QA, Team Lead) Free Meals and Snacks at office locations How to Apply: Please send your updated resume certification details and current notice period to: Email Id - amith.baswaraj@coronishealth.com Contact No - Amith G - 8971789084 Subject: Application Specialty Coder [Your Name] (e.g., Application General Surgery Coder – Priya R) Regards , Amith G

Omega Healthcare is hiring Medical Coders and Quality Control Analysts!! Job Role Description Overview: Coder is accountable to manage day to day activities of coding the Patients chart & Diagnosis report. Responsibility Areas: Coding or auditing charts, based on requirements Updating/Clearing the production/pending reports To work closely with the team leader. To review emails for any updates Identify issues and escalate the same to the immediate supervisor Strict adherence to the company policies and procedures. Sound knowledge in Medical Coding concept. Should have minimum 1 year of Coding Experience. Understand the client requirements and specifications of the project. Meet the productivity targets of clients within the stipulated time (Daily & Monthly) Applying the instructions/updates received from the client during production. Coding or auditing charts, based on requirements. Prepare and Maintain reports. *Chennai Vacancies* 1.EM IP OP Coders / QCA 2.Radiology Coders 3.IPDRG Coders / Quality Control Auditors 4. Multi-Specialty Denial Coders 5.IVR Radiology Coders 6.Home Health Quality Control Auditors 7.Surgery Coder/Quality Control Analysts *Bengaluru Vacancies* 1.Home Health Quality Control Auditors Experience - For Coders - Minimum 1 year is required For QCA - Minimum 3 years is required. Note: *Certification (CPC/CIC/CCS) is mandatory for all specialties except Home Health. Mode - Work from Office. Notice Period: 0 - 15 days Interested candidates can share their updated resume at vigneshwar.chawan@omegahms.com or WhatsApp at 9963068969 / syed.azeez@omegahms.com or WhatsApp at 8073452491

Greetings from CorroHealth! We are Hiring! AVP Medical Coding Company Name: CorroHealth Location: Hyderabad Job Type: Full-time Experience Level: 17+ Years About Us CorroHealth is the leading provider of clinically led healthcare analytics and technology-driven solutions dedicated to positively impacting the financial performance of hospitals and health systems. CorroHealth delivers integrated solutions, proven expertise, intelligent technology, and scalability to address needs across the entire revenue cycle. We started our journey in 2006 with a 4-member team, today we stand at 14000+ global pool and are thriving at 7 locations across India & US and is headquartered at Chennai. Job Description We are seeking a highly skilled and experienced AVP Medical Coding professional to join our team at the Noida location. The ideal candidate will have over 17+ years of experience in medical coding, with a proven track record of managing large teams of 250 to 600 coders. The candidate should be certified from AAPC or AHIMA, with strong leadership capabilities, client handling experience, and a deep understanding of the healthcare and medical coding industry. The candidate's current designation should be a Director or Associate Director. Key Responsibilities: Oversees the daily operations of the coding unit including workload and staffing; hiring, disciplining, and performance appraisals; training; and monitoring quality of work. Develops long-range and short-term goals, objectives, plans, and programs and ensures they are implemented. Assists in planning, developing, and controlling the budget, including staffing costs, capital equipment, and operations of the coding unit. Evaluates the impact of innovations and changes in programs, policies, and procedures for the coding unit. Designs and implements systems and methods to improve data accessibility. Identifies, assesses, and resolves problems. Prepares administrative reports. Oversees and monitors the coding compliance program. Develops and coordinates educational and training programs regarding elements of the coding compliance program such as appropriate documentation and accurate coding to all appropriate staff. Ensures the appropriate dissemination and communication of regulatory, policy, and guideline changes. Conducts and oversees coding audit efforts and coordinates monitoring of coding accuracy and documentation adequacy. Reports non-compliance issues detected through auditing and monitoring, the nature of corrective action plans, and the results of follow-up audits. Conducts trend analyses to identify patterns and variations in coding practices. Reviews claim denials and rejections pertaining to coding and medical necessity issues and, when necessary, implements corrective action plan to prevent similar denials and rejections from recurring. What We Are Looking For: Educational Qualification: Any Graduate (Preferably from Life Science background) Experience: 17+ years of experience in Multispecialty Coding and substantial team management experience. Excellent communication skills, both verbal and written. Strong managerial, leadership, analytical, interpersonal skills and Outstanding organizational skills. Hands on Experience in generating reports using MS Office - Excel, word and MS power point. Why Join Us? At CorroHealth, we believe in high values and the best work culture. Our team is diverse, creative, and dedicated to making an impact. We offer: Competitive salary Health insurance options Flexible working hours Opportunities for professional growth Inclusive, collaborative environment Interested aspirants kindly share your updated resume to bhuvaneswari.mohan@corrohealth.com or Contact - 9150006744

CGreetings from Coronis Ajuba (Formerly known as MiraMed Ajuba) We are looking for Experienced certified Surgery & IPDRG medical Coders and Auditors to join us. Interested candidates please call us @ 91+ 6385272597 or mail to manojprassana.dillibabu@coronishealth.com to book interview slot. SURGERY Coders & Auditors (2 to 10 Years) * Certified People only * Experience : 1+ yrs of experience in Surgery (Same day Surgery or General Surgery) * Location : Chennai & Hyderabad * Work from Office * Competitive Salary with Food and other Benefits. * Immediate joiners IPDRG Coders & Auditors (2 to 15 Years Certified People only * Experience : 1+ yrs of experience in IPDRG * Location : Chennai & Hyderabad * Work from Office * Competitive Salary with Food and other Benefits. * Candidates with 2 months notice period can also Apply Attractive Salary for immediate joiners. Grab the opportunity and refer your friends Interested Candidates send you resume to the below WhatsApp Number or Reach me out on 6385272597 Regards, Manoj - 6385272597 Human Resources Coronis Ajuba

We Hiring EM IP/OP Coders/QA Min 3+ Yr of Experience required Certification is Mandatory Education - Only Life Science background Good knowledge in ICD-10, CPT, Modifiers and ETC.., WFO is must. Location: Chennai Contact - 9344402033 Keerthiga

Role & responsibilities WE ARE HIRING MEDICAL CODERS & QA PROFESSIONALS CODER LEVEL (Min 2 Years Exp): Surgery Coder Hyderabad, Chennai, Noida, Bangalore – Up to 60K • ENM Multispecialty – Chennai – Up to 10 LPA • ENM Denial – Chennai – Up to 10 LPA • Radiology – Chennai – Up to 10 LPA • ENM Coder – Chennai, Bangalore – Up to 50K QA LEVEL (Min 4 Years Exp): Surgery QA – Hyderabad, Chennai, Bangalore – Up to 70K • ENM QA – Bangalore, Chennai – Up to 60K Certification : CPC / CCS / CIC / COC – Any One Mandatory Relieving Letter : Mandatory Notice Period : Immediate to 30 Days (Preferred: Immediate Joiners) Work Mode : Work From Office Only Interested Candidates Contact HR Sujitha – 8297250813 Preferred candidate profile

We're Excellent Hiring! Certified Medical coding Location: Chennai/Coimbatore/Pune "CERTIFICATION IS MANDATORY" Denial Coders : Chennai | Coimbatore |Pune (Certified) EM OP Coders : Chennai | Coimbatore | Pune (Certified) Surgery Coders : Chennai |Coimbatore | Pune (Certified) ED Facility Coder: Chennai |Coimbatore |Pune (Certified) Radiology Coder : Chennai (Certified) > Minimum 1 year experience needed > Salary as per market standards > Only for certified coders > Relieving letter is not mandatory > Preferably Immediate > 10to15 days' notice period acceptable Freshers not eligible Salary as per market standards 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, kowsalya Recruiter Talent Acquisition | Access HealthCare m: 8122343331 w: www.accesshealthcare.com

Job Title: HPDC Process Engineer Location: Multiple Sites Across India Experience Required: 5 to 10 Years Employment Type: Full-Time Industry: High Pressure Die Casting (HPDC) Company: Steady Die Casting Solutions (SDS) Job Description: Steady Die Casting Solutions (SDS) is looking for a High Pressure Die Casting (HPDC) Process Engineer with 5–10 years of hands-on experience in die casting machine operation, process parameter setup, and logical troubleshooting. The ideal candidate must have a strong grasp of machine parameters, their impact on casting quality, and a scientific mindset towards process stability and defect resolution. This role demands independent execution at customer sites across India, ensuring HPDC process consistency, quality improvement, and technical support. SDS will provide complete training in HPDC Process Control and Monitoring , and empower you with advanced skills, tools, and techniques for professional growth. Key Responsibilities: Set and validate critical HPDC machine and process parameters (shot control, pressure, speed, temperature, etc.). Analyze casting defects using a logical, data-driven approach. Conduct root cause analysis (RCA) and implement corrective and preventive actions (CAPA). Collaborate with toolroom, maintenance, and quality teams to ensure stable production. Provide on-site process support and guidance to client facilities across India. Monitor and document process trends, deviations, and improvements. Participate in process audits and SOP development. Actively contribute to SDS’s mission of improving HPDC process control and performance. Undergo and apply SDS's in-house advanced training modules. Qualifications: Diploma or Degree in Mechanical Engineering or relevant field. 5–10 years of hands-on experience in High Pressure Die Casting (preferably with exposure to 250T to 1300T machines). Strong knowledge of machine and process parameters and their effect on casting quality. Ability to work independently and travel to multiple customer locations. Logical mindset and problem-solving attitude with scientific thinking. Basic understanding of quality tools (5 Why, Pareto, Cause-Effect, etc.) preferred. Willingness to learn and adapt to advanced monitoring and control systems. What SDS Offers: Hands-on HPDC Process Control & Monitoring Training . Opportunity to work on complex die casting problems across India. Skill enhancement through the latest tools, machines, and AI-based solutions. Independent role with leadership exposure and long-term growth prospects. How to Apply: Send your resume with the subject "Application for HPDC Process Engineer" to hpdc@hpdcpathshala.com

Greetings from Medical Billing Wholesalers... Location: Chennai (WFO) Experience: 1-5 Years Key Skills: Surgery Coder, Denial Coder, Anesthesia Coder Note: No Cross Training Interested can contact : Gowri - 7708462567 / Lavanya - 7871090718 Desired Candidate Profile: Certification: Certified or Non certified Experience:1- 5 years in Medical Coding Strong knowledge of ICD-10, CPT. Excellent analytical and communication skills Job Description: We are hiring experienced Medical Coders with strong expertise in: Denial Coding: Review and resolve coding-related denials from payers; work on appeals and resubmissions. or Surgery Coding: Accurately code complex surgical procedures using CPT, ICD-10-CM, and HCPCS in accordance with NCCI and payer-specific guidelines . or Anesthesia Coding: Assign correct anesthesia CPT codes using ASA Crosswalks , apply appropriate modifiers (e.g., QS, AA, QX) , and calculate anesthesia time and base units

Greetings from AGS Health. Designation: Medical Coder/Senior Medical coder Speciality we are hiring: E/M OP, ED Profee, Denials, Surgery, IPDRG, Job Description : Should have knowledge in Medical Coding concept. Understand the client requirements and specifications of the project. Meet the productivity targets of clients within the stipulated time (Daily & Monthly) Applying the instructions/updates received from the client during production. Coding or auditing charts, based on requirements. Prepare and Maintain reports Good Knowledge on Anatomy & Physiology Excellent Knowledge on ICD & CPT Good Computer Skills Above Average Communication Skills Good Reporting Skills Requirements and Skills: Experience: 1 + Years of experience in above mentioned speciality Work Location - Ambattur, Kandanchavadi (Work from office) Salary Offered: Based on your experience Minimum Qualification: Life Science/ paramedics, Graduates. License/Certification: CPC, CIC, COC,CCS (Required) Evaluation & Management - OP : Minimum 12 months experience in EM - OP/IP, ED Profee, ED facility, Denials, surgery, IPDRG. Certification is Mandatory. Preferably immediate joiners. Interview Mode: Virtual Benefits: Health insurance Provident Fund Day shift One way cab facilities + breakfast If your are interested please send me your updated resume to this number in Whatsapp - 7397238884 or send to this mail ID - mohanasundari.sowndarrajan@agshealth.com Thanks & Regards Mohanasundari HR -TA AGS HEALTH

Hiring Medical coders||UP TO 10 LPA || Min 3 yr of exp in below mentioned specialisation's Surgery - Hyderabad,Chennai,Bangalore,Noida Radiology - Chennai Denials Multispeciality - Chennai ENM Multispeciality - Chennai ENM IP OP Observation - Chennai ENM with Surgery - Chennai IPDRG - Hyderabad, Chennai, Bangalore ENM - Chennai, Bangalore OBGYN - Chennai Only certified coders Up to 10 LPA Notice Period : 0-30 Days Relieving letter is mandatory Interested candidates can drop Your Resume To: HR Lalitha - 8179142981 through Whatsapp lalithahr.axis@gmail.com through Mail References are highly appreciated.

We are seeking a motivated Biotechnology lab Associate to join our Product Development 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 Responsibilities 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 . Documentation & Compliance Maintain detailed records of experimental protocols, QC data, and client reports . Ensure compliance with ISO or other regulatory standards (if applicable). 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 (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 . Knowledge of regulatory standards (ISO 13485, GMP). Fluency in English + regional Indian languages (Hindi 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 District, Uttar Pradesh: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Minimum Salary Expectation: Education: Bachelor's (Preferred) Work Location: In person

Designation – Senior Research Associate Location: Sahibabad, Ghaziabad Preferred Qualifications (Full time): · M.Sc. (Microbiology/Industrial Microbiology/Biotechnology) Experience Range and Knowledge: 2 – 3 years post qualification Job Responsibilities: Experienced candidate with proven analytical skills and track record of delivery Proficient in all basic microbiology tools and techniques for handling bacteria, yeast an fungi. Hands on experience in microbiology lab techniques like sterilization, aseptic techniques, serial dilution, inoculation, streaking, screening and isolation of microbes, staining techniques, biochemical and morphological tests for microbial identification, microscopy, cell enumeration, MIC studies Experience in handling strictly anaerobic and pathogenic microbes Knowledge of industrial bio-processes like alcoholic fermentation, biogas production, food and beverages industry, wastewater treatment etc. Knowledge of molecular techniques like gel electrophoresis, gel documentation, SDS PAGE, DNA isolation etc Knowledge of industrial enzymes and their applications Fair understanding of ISO 9001, Lab safety & GLP management Microsoft office, Documentation and reports preparation Good communication skills (oral and written) Job Types: Full-time, Permanent Pay: ₹400,000.00 - ₹500,000.00 per year Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Experience: Analytical Skills: 2 years (Required) Microbiology tools & techniques: 2 years (Required) Microbiology lab techniques: 2 years (Required) MIC Studies: 2 years (Required) SDS Page: 2 years (Required) GLPC: 2 years (Required) ISO 9001: 2 years (Required) Work Location: In person

Job Title: Senior Steel Detailing Professional Location: Cochin | Coimbatore | Bangalore (Whitefield) Employment Type: Full-Time Job Description: We are seeking experienced and passionate professionals in Steel Detailing who are eager to create a meaningful impact in the structural engineering industry. The ideal candidate should have hands-on expertise in Tekla and SDS/2 software and a proven track record in leading and managing detailing teams. Key Responsibilities: Execute and oversee steel detailing projects with precision and quality. Lead and mentor a team of detailers, ensuring timely delivery of projects. Coordinate with internal and external stakeholders to ensure project success. Maintain compliance with industry standards and client specifications. Requirements: Strong experience in steel detailing, preferably with leadership experience. Proficiency in Tekla Structures or SDS/2 software is a must. Strong team management and communication skills. Ability to handle multiple projects and deadlines efficiently. Willingness to work from Cochin, Coimbatore, or Bangalore (Whitefield) only candidates open to these locations should apply. What We Offer: Opportunity to work on impactful projects. A dynamic and supportive work environment. Career growth and leadership opportunities in the steel detailing industry. Interested candidates may share their updated resume with us. Lets build the future of steel detailing together!

Job title: Safety Data Sheets expert Location: Hyderabad About The Job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions. As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health. The Global M&S Services acts as a cornerstone to this effort. Our team is responsible for delivering and supporting M&S teams in the area of regulatory compliance, maintenance of product licenses and technical writing of CMC documents. The team members of the global M&S Services Hub will act as partners in carrying out tasks and fulfilling responsibilities to support quality activities with a focus on technical writing. Main Responsibilities Provision of strategic advice to the businesses with regards to regulatory compliance linked to substances (e.g. safety data sheets, classification, packaging & labelling, transport classification, local regulations). This includes monitoring of regulations. Act with efficiency with the Global Product Stewardship team. Edit and maintain Safety Data Sheets using our IT tools. Independent evaluation and validation of substance data for classification and labelling according to international regulations e.g., GHS/CLP, Seveso, and transport regulations. Documents all product stewardship information including references, reports to track and to justify any modification in the versioning of the documents used by Product Stewardship (SDSs, Hazard Classification Sheets & data). Conducting substance data searches and evaluating the results. Collecting, documenting and providing data in internal substance databases. Communicating effectively in a written and oral ways results & conclusions with contacts of sites and Business Units. About You Experience: 5+ years of industry experience including 2+ years’ experience in Product Stewardship. Soft skills: Be able to work effectively in a team and on your own initiative. Self-starter with the ability to perform under rapidly evolving contexts. Data-based decision maker and methodical in the analysis. Good coordination and communication skills. Ability to provide clear concise explanations. Have critical thinking, problem solving & planning skills. Able to work independently, team player and networker. Important sense for transversal impact. Ability to communicate effectively, orally and in writing. Technical skills: SDS-Writing - Certified competent person according to 18 (4) Hazard Substance Ordinance (Germany) Proficiency in SAP-EHS module is needed. Proven experience of interactions of SAP-EHS with SAP based ERP is needed. Proven experience of SERC – SAP EHS Regulatory Content (now 3E ERC EHS Regulatory Content) is needed. Certified IATA training for Dangerous Goods Transportation is needed. Proven knowledge on toxicological / pharma toxicological backgrounds would be a plus. Knowledge in the use of Artificial Intelligence for the use of designing SDSs would be a plus (e.g. tool from Opesus). Experience on Extended SDS would be a plus. Knowledge on Biocides and in biological agents would be a plus. Professional experience in the field of product safety/product stewardship, chemical laws, classification and labelling of hazardous substances. Experience in writing and reading Material Safety Data sheets. Education: Bachelor’s degree in science or Technical discipline at minimum. Languages: Verbal and written fluency in English Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention, and wellness programs and at least 14 weeks’ gender-neutral parental leave. Opportunity to work in an international environment, collaborating with diverse business teams and vendors, working in a dynamic team, and fully empowered to propose and implement innovative ideas. null Pursue Progress . Discover Extraordinary . Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together. At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

Job title: Safety Data Sheets Manager Location: Hyderabad About The Job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions. As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health. The Global M&S Services acts as a cornerstone to this effort. Our team is responsible for delivering and supporting Global M&S teams in the area of regulatory compliance, maintenance of product licenses and technical writing of CMC documents. The team members of the global M&S Services Hub will act as partners in carrying out tasks and fulfilling responsibilities to support global quality activities with a focus on technical writing. Main Responsibilities Management of a team experts with purpose to improve the performance of management of Safety Data Sheets and specifications within SAP-EHS. As a manager, you are responsible for the process of managing Safety Data Sheets in due time to prevent occupational / environmental/ Process safety events which may lead to business interruption Provision of strategic advice to the businesses regarding regulatory compliance linked to substances (e.g. safety data sheets, classification, packaging & labelling, transport classification, local regulations). This includes monitoring of regulations Act with efficiency with the Global Product Stewardship team. Edit and maintain Safety Data Sheets using our IT tools. Independent evaluation and validation of substance data for classification and labelling according to international/local regulations e.g., GHS/CLP, Seveso, and transport regulations. Document all product stewardship information including references, reports to track and to justify evolutions in the versioning (SDSs, Hazard Classification Sheets & data), that support SDS decision. Conducting substance data searches and evaluating the results. Collecting, documenting and providing data in internal substance databases. Communicating effectively in a written and oral ways results & conclusions with contacts of sites and Business Units. About You Experience: 10+ years of industry experience including 5+ years’ experience in Product Stewardship. 2 years of experience to lead a group in the EHS field. Soft skills: Professional experience in the field of product safety/product stewardship, chemical laws, classification and labelling of hazardous substances. Experience in writing and reading Material Safety Data sheets. Ability to rank relative compliance risks, high sense of responsibility and compliance and prioritize resulting actions. Ability to keep abreast of compliance changes. Strong proficiency in common chemical regulations. Ability to provide clear concise explanations. Have critical thinking, problem solving & planning skills. Technical skills: Knowledge in national regulatory aspects according ECHA Guidance for the editing of SDSs. Proficiency in SAP-EHS module is needed. Proven experience of interactions of SAP-EHS with SAP based ERP is needed. Proven experience of SERC – SAP EHS Regulatory Content (now 3E ERC EHS Regulatory Content) is needed. Certified IATA training for Dangerous Goods Transportation is needed. Proven knowledge on toxicological / pharma toxicological backgrounds would be a plus. Knowledge in the use of Artificial Intelligence for the use of designing SDSs would be a plus (e.g. tool from Opesus). Experience on Extended SDS. Knowledge on Biocides would be a plus. Knowledge in biological agents / biosafety would be a plus. Education: Master’s degree in science or Technical discipline at minimum. Languages: Verbal and written fluency in English Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention, and wellness programs and at least 14 weeks’ gender-neutral parental leave. Opportunity to work in an international environment, collaborating with diverse business teams and vendors, working in a dynamic team, and fully empowered to propose and implement innovative ideas. null Pursue Progress . Discover Extraordinary . Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together. At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

We're Excellent Hiring! Certified Medical coding Location: Chennai/Coimbatore/Pune "CERTIFICATION IS MANDATORY" Denial Coders : Chennai | Coimbatore |Pune (Certified) EM OP Coders : Chennai | Coimbatore | Pune (Certified) Surgery Coders : Chennai |Coimbatore | Pune (Certified) ED Facility Coder: Chennai |Coimbatore |Pune (Certified) Radiology Coder : Chennai (Certified) > Minimum 1 year experience needed > Salary as per market standards > Only for certified coders > Relieving letter is not mandatory > Preferably Immediate > 10to15 days' notice period acceptable Freshers not eligible Salary as per market standards Interview Mode: Virtual Work mode: WFO/WFH both available Contact: HR Lavanya - 9344964267 (Interested please share your resume to mentioned number) Refer and share with someone who might be a great fit! Regards, Lavanya HR Recruiter Talent Acquisition | Access HealthCare m: 9344964267 e: lavanya.v10@accesshealthcare.com w: www.accesshealthcare.com

Job title: Safety Data Sheets Manager Location: Hyderabad About the job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions. As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health. The Global M&S Services acts as a cornerstone to this effort. Our team is responsible for delivering and supporting Global M&S teams in the area of regulatory compliance, maintenance of product licenses and technical writing of CMC documents. The team members of the global M&S Services Hub will act as partners in carrying out tasks and fulfilling responsibilities to support global quality activities with a focus on technical writing. Main responsibilities: Management of a team experts with purpose to improve the performance of management of Safety Data Sheets and specifications within SAP-EHS. As a manager, you are responsible for the process of managing Safety Data Sheets in due time to prevent occupational / environmental/ Process safety events which may lead to business interruption Provision of strategic advice to the businesses regarding regulatory compliance linked to substances (e.g. safety data sheets, classification, packaging & labelling, transport classification, local regulations). This includes monitoring of regulations Act with efficiency with the Global Product Stewardship team. Edit and maintain Safety Data Sheets using our IT tools. Independent evaluation and validation of substance data for classification and labelling according to international/local regulations e.g., GHS/CLP, Seveso, and transport regulations. Document all product stewardship information including references, reports to track and to justify evolutions in the versioning (SDSs, Hazard Classification Sheets & data), that support SDS decision. Conducting substance data searches and evaluating the results. Collecting, documenting and providing data in internal substance databases. Communicating effectively in a written and oral ways results & conclusions with contacts of sites and Business Units. About you: Experience: 10+ years of industry experience including 5+ years experience in Product Stewardship. 2 years of experience to lead a group in the EHS field. Soft skills: Professional experience in the field of product safety/product stewardship, chemical laws, classification and labelling of hazardous substances. Experience in writing and reading Material Safety Data sheets. Ability to rank relative compliance risks, high sense of responsibility and compliance and prioritize resulting actions. Ability to keep abreast of compliance changes. Strong proficiency in common chemical regulations. Ability to provide clear concise explanations. Have critical thinking, problem solving & planning skills. Technical skills : Knowledge in national regulatory aspects according ECHA Guidance for the editing of SDSs. Proficiency in SAP-EHS module is needed. Proven experience of interactions of SAP-EHS with SAP based ERP is needed. Proven experience of SERC - SAP EHS Regulatory Content (now 3E ERC EHS Regulatory Content) is needed. Certified IATA training for Dangerous Goods Transportation is needed. Proven knowledge on toxicological / pharma toxicological backgrounds would be a plus. Knowledge in the use of Artificial Intelligence for the use of designing SDSs would be a plus (e.g. tool from Opesus). Experience on Extended SDS. Knowledge on Biocides would be a plus. Knowledge in biological agents / biosafety would be a plus. Education: Master s degree in science or Technical discipline at minimum. Languages : Verbal and written fluency in English Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention, and wellness programs and at least 14 weeks gender-neutral parental leave. Opportunity to work in an international environment, collaborating with diverse business teams and vendors, working in a dynamic team, and fully empowered to propose and implement innovative ideas.

Job title: Safety Data Sheets expert Location: Hyderabad About the job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions. As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health. The Global M&S Services acts as a cornerstone to this effort. Our team is responsible for delivering and supporting M&S teams in the area of regulatory compliance, maintenance of product licenses and technical writing of CMC documents. The team members of the global M&S Services Hub will act as partners in carrying out tasks and fulfilling responsibilities to support quality activities with a focus on technical writing. Main responsibilities: Provision of strategic advice to the businesses with regards to regulatory compliance linked to substances (e.g. safety data sheets, classification, packaging & labelling, transport classification, local regulations). This includes monitoring of regulations. Act with efficiency with the Global Product Stewardship team. Edit and maintain Safety Data Sheets using our IT tools. Independent evaluation and validation of substance data for classification and labelling according to international regulations e.g., GHS/CLP, Seveso, and transport regulations. Documents all product stewardship information including references, reports to track and to justify any modification in the versioning of the documents used by Product Stewardship (SDSs, Hazard Classification Sheets & data). Conducting substance data searches and evaluating the results. Collecting, documenting and providing data in internal substance databases. Communicating effectively in a written and oral ways results & conclusions with contacts of sites and Business Units. About you: Experience : 5+ years of industry experience including 2+ years experience in Product Stewardship. Soft skills: Be able to work effectively in a team and on your own initiative. Self-starter with the ability to perform under rapidly evolving contexts. Data-based decision maker and methodical in the analysis. Good coordination and communication skills. Ability to provide clear concise explanations. Have critical thinking, problem solving & planning skills. Able to work independently, team player and networker. Important sense for transversal impact. Ability to communicate effectively, orally and in writing. Technical skills : SDS-Writing - Certified competent person according to 18 (4) Hazard Substance Ordinance (Germany) Proficiency in SAP-EHS module is needed. Proven experience of interactions of SAP-EHS with SAP based ERP is needed. Proven experience of SERC - SAP EHS Regulatory Content (now 3E ERC EHS Regulatory Content) is needed. Certified IATA training for Dangerous Goods Transportation is needed. Proven knowledge on toxicological / pharma toxicological backgrounds would be a plus. Knowledge in the use of Artificial Intelligence for the use of designing SDSs would be a plus (e.g. tool from Opesus). Experience on Extended SDS would be a plus. Knowledge on Biocides and in biological agents would be a plus. Professional experience in the field of product safety/product stewardship, chemical laws, classification and labelling of hazardous substances. Experience in writing and reading Material Safety Data sheets . Education : Bachelor s degree in science or Technical discipline at minimum. Languages : Verbal and written fluency in English Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention, and wellness programs and at least 14 weeks gender-neutral parental leave. Opportunity to work in an international environment, collaborating with diverse business teams and vendors, working in a dynamic team, and fully empowered to propose and implement innovative ideas.