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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.

Role & responsibilities Were Hiring! Medical Coders & QA Professionals Open Roles Coder Level Surgery Coder | Up to 60K TH | Min 1 yr exp | Hyderabad , Chennai, Bangalore, Noida Radiology Coder | Up to 7.5 LPA | Min 1 yr exp | Chennai Multispecialty Denial Coder | Up to 10 LPA | Min 3 yrs exp | Chennai E&M OP Coder | Up to 50K TH | Min 1 yr exp | Bangalore, Chennai IPDRG Coder | Up to 90K TH | Min 2 yrs exp | Hyderabad, Chennai QA Level Roles Surgery QA | Up to 70K TH | Min 4+ yrs exp | Chennai, Bangalore E&M QA | Up to 60K TH | Min 4 yrs exp | Bangalore, Chennai IPDRG QA | Up to 1L TH | Min 4 yrs exp | Hyderabad, Chennai E&M with Surgery QA | Up to 12.5 LPA | Min 5 yrs exp | Chennai Locations : Hyderabad | Chennai | Bangalore | Noida Notice Period : 030 Days (Immediate Joiners Preferred) Certifications : CPC / CIC / COC / CCS (Any) Relieving Letter : Not Mandatory Looking to take the next step in your coding career? Reach out to HR Prathyusha 7702498242 for more details. Preferred candidate profile

We're 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) > 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 SAMEEMA-7339689430 (Interested please share your resume to mentioned number) Refer and share with someone who might be a great fit! Regards, Sameema Begam.M Recruiter Talent Acquisition | accesshealthcare m: 7339689430 e: sameemabegum.m@accesshealthcare.com w: www.accesshealthcare.com

Hi All, We have a urgent Opening for SME Medical Coder Specialization - SDS Surgery CTC - 11.5 LPA Location - Noida If anyone Interested Call me on 9820389632 OR share me your resume at vinoda@phebushr.com

Greetings from Happiehire !!! Open Positions: EM OP Ancillary coding Same day surgery coding ED facility EM multispeciality Requirement: Candidate Should have Experience of Min 2years in any of the above specialties. Should have valid coding certification(CPC,CCS) Need Proper Releiving from all the Companies & Must Have PF Account. Work from office (Banglore & Chennai location) Interested Candidates can Share Resumes to Vedha Mithra HR 9010608096.

Dear Candidates, Greetings from ExxonMobil! Job Title - Regulatory Business Compliance Advisor - PE/ PP Products Please copy and paste the below link into your browser to apply for the position in the company website. Link to apply: https://jobs.exxonmobil.com/job-invite/80881/ Please find the JD below, 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) Thanks, Anita Bhati.

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.

Position: Skincare Formulator (Laboratory-Based) Location: Ahmedabad Company: Dermatouch – www.dermatouch.com Key Responsibilities: 1. Formulation Development: Develop and optimize skincare formulations including creams, serums, gels, emulsions, and cleansers. Select appropriate emulsifiers, humectants, preservatives, and actives for performance and stability. Conduct pre-formulation and compatibility studies, pH balancing, and HLB optimization. Troubleshoot formulation challenges like phase separation, viscosity changes, and air entrapment. 2. Testing & Analysis: Perform stability testing under varied conditions (4°C to 45°C, freeze-thaw). Conduct microbial, preservative efficacy (challenge) tests, and oxidative stability. Carry out rheological, sensorial, and active ingredient efficacy testing using tools like HPLC, FTIR, viscometers, and diffusion studies. 3. Regulatory Compliance & Documentation: Ensure compliance with cosmetic regulations (FDA, EU 1223/2009, ISO 22716). Prepare and maintain Product Information Files (PIFs), SDS, and ingredient justifications. Collaborate with toxicologists for HRIPT/in-vitro safety assessments. 4. Manufacturing Support: Prepare BMRs and MFRs in line with SOPs and GLP practices. Support scale-up from lab to pilot/production batches. Troubleshoot production issues and validate first commercial batches. 5. Innovation & Research: Stay up to date with new ingredients, green chemistry trends, and advanced formulation techniques. Benchmark competitor products and collaborate with vendors for novel raw materials. Required Qualifications: Bachelor’s/Master’s/Ph.D. in Cosmetic Science, Chemistry, Pharma, Biochemistry, or Chemical Engineering. 3–5+ years of experience in cosmetic formulation/R&D. Familiarity with GMP/ISO-certified labs and formulation software (e.g., Cosmetic Factory, ChemSketch). Strong analytical, documentation, and cross-functional collaboration skills.

Walk-In Interview for Experienced Medical Coders at Vee Healthtek, Chennai on July 12 & 13 Experience : 1 to 7 Years experience on medical coding Specialty : IP DRG/Surgery/EM/ED/Radiology/IVR/Anesthesia- Medical Coding Job Location : Chennai, Bangalore, Salem,Trichy, Hyderabad & Pune - Work From Office Designation : Medical Coder/Sr Coder/QA/GC/TC AAPC Certification is Must Interview Schedule : July 12 & 13 at 11:00 TO 1PM Interview Venue: Vee Healthtek Pvt Ltd, Tower-3 Special Module, Chennai One IT Park SEZ, Pallavaram to Thoraipakkam 200 Feet Road, Thoraipakkam, Chennai - 600 097 Important Note : Please mention my name, Kalaiyarasi HR as Reference, at the top of your resume. Contact Information: Kalaiyarasir- 9566406546(Available on WhatsApp) kalaiyarasi.r@veehealthtek.com Regards Kalaiyarasi - HRD Vee HealthTek

Greetings from AGS Health. Designation: Medical Coder/Senior Medical coder/ QA Speciality we are hiring: E/M OP, ED Profee, Denials, Surgery, IPDRG, Anaesthesia 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, Anaesthesia Certification is Mandatory. Preferably immediate joiners. Interview Mode: Virtual Benefits: Health insurance Provident Fund Day shift One way cab facilities + breakfast Thanks & Regards Sopphiya Anbu HR -TA AGS HEALTH

We are Hiring "Medical Coders" ,Trainers and QA Qualification: Any Degree Specializations : 1. IPDRG Coder : Hyderabad / Chennai || CTC upto 13 LPA || 2. Surgery Coder : Chennai / bangalore/ Bangalore/ Noida || CTC upto 10 lpa || 3. Denials : Chennai / Hyderabad || CTC upto 10 lpa || 4. Radiology : Chennai || CTC upto 7.5 lpa|| 5. ENM : Chennai / bangalore || CTC upto 5 lpa || 6. IVR Radiology : Chennai / Hyderabad ||CTC upto 10 lpa | 7. Obgyn : Hyderabad || CTC upto 10 lpa || 8. Ed blended : Hyderabad || CTC upto 10lpa || 9. IPDRG QA : Hyderabad/ Chennai || CTC upto 12 lpa 10. EM / IPDRG / Denials trainer : Hyderabad/ Chennai || CTC upto 18 lpa Experience : Minimum 1 year relevant experience is mandatory If you are interested, ping me or share your updated resume to_ Whatsapp or call GEETHANJALI HR - 7093149635 Email: geethanjali.axisservices@gmail.com

Industrial Post-Doctoral Fellow-HPLC Method Development (Protein Biologics) About Mynvax Mynvax is a clinical-stage vaccine biotechnology company headquartered in Bangalore, India, developing novel, recombinant, and thermostable vaccines against respiratory viral infections, including influenza and RSV. With a pipeline of promising candidates and multiple ongoing collaborations, Mynvax offers a unique opportunity to work at the cutting edge of vaccine development. Role Design, develop, and optimize HPLC/UPLC methods (e.g., SEC, RP-HPLC, IEX, HIC) for protein characterization, including purity, aggregation, charge variants, and stability. Conduct protein analysis using HPLC and orthogonal techniques for in-process and final DS samples. Interpret results, troubleshooting analytical challenges, and ensure data quality and integrity. Prepare analytical protocols, reports, and SOPs, and contribute to method development and qualification. Collaborate with upstream, downstream, and formulation development teams. Support regulatory submissions with high-quality analytical documentation. Required Qualifications Ph.D. in Biophysics, Biochemistry, Analytical Chemistry, Biotechnology, or a related field. Hands-on experience in HPLC method development for proteins (during Ph.D. or postdoc). Basic understanding of protein structure, behavior, and physicochemical properties. Familiarity with HPLC data acquisition and analysis software (e.g., Openlab CDS, Empower, ChemStation). Desirable Skills Knowledge of ICH Q2/WHO guidelines for analytical method validation. Experience with protein biologics, vaccine antigens, or biosimilar analytics. Familiarity with other techniques such as CE, SDS-PAGE, Western blotting, or ELISA. What Mynvax offers: A stimulating industrial research environment with real-world impact. Exposure to state-of-the-art technologies and multidisciplinary collaboration. Mentorship and professional development support from experienced scientists. Full-time salary and benefits include health coverage, generous leave package, and statutory entitlements. Location: Bangalore, India Company: Mynvax Private Limited Position Type: Full-Time | Fixed Term (12-24 months, extendable) Start Date: Immediate Compensation: Competitive salary with full-time employee benefits How to apply: Email your CV and a brief cover letter to careers@mynvax.com Subject line: "Post-Doctoral Fellow-HPLC Application" Apply on LinkedIn: Post-Doctoral Fellow-HPLC Application

1.Tekla Modelers - 4 to 7 years of experience - 4 openings2.Tekla Editors - 1 to 4 years of experience - 8 openings3.Tekla Checkers - 2 to 8 years of experience - 3 openings4.Freshers - Diploma or Engineering in Civil/Mechanical - 15 openings Posted 4 hours ago View Details

Robert Bosch Engineering and Business Solutions Private Limited is looking for Sr. BT Developer_SDS/BSV - ENG to join our dynamic team and embark on a rewarding career journey. Design, develop, and maintain backend and integration components for SDS/BSV engineering systems. Collaborate with business and technical teams to understand requirements and translate them into robust code. Ensure seamless communication between systems via APIs and middleware. Implement best practices for code quality, security, and performance optimization. Troubleshoot and debug issues across development and production environments. Provide documentation and support for code releases and deployments. Lead junior developers and review code for adherence to standards. Participate in Agile ceremonies and contribute to continuous improvement initiatives.

Mynvax is a clinical-stage vaccine biotechnology company headquartered in Bangalore, India, developing novel, recombinant, and thermostable vaccines against respiratory viral infections, including influenza and RSV. With a pipeline of promising candidates and multiple ongoing collaborations, Mynvax offers a unique opportunity to work at the cutting edge of vaccine development. Role Perform gene cloning using various strategies including restriction/ligation, Gibson Assembly, and Golden Gate. Carry out site-directed mutagenesis and construct verification. Design and run PCR assays for amplification and screening. Prepare and submit samples for Sanger sequencing; analyze sequencing results. Express recombinant proteins in E. coli or other expression systems. Run SDS-PAGE and Western blotting for protein expression and analysis. Maintain accurate and detailed lab records; ensure reproducibility and quality of experimental data. Collaborate with team members involved in antigen production and vaccine R&D. Required Qualifications M.Sc. or M.Tech. in Molecular Biology, Biotechnology, Microbiology, or related field. 0-3 years of hands-on experience in molecular biology techniques. Experience with cloning methods including restriction/ligation, Gibson Assembly, Golden Gate, and site-directed mutagenesis. Basic understanding of recombinant protein expression workflows. Familiarity with PCR, gel electrophoresis, and gel-based detection methods. Desirable Skills Experience in bacterial transformation, plasmid preparation, and cloning troubleshooting. Experience with mammalian and insect cells expression systems. Knowledge of protein purification techniques such as Ni-NTA affinity chromatography. Familiarity with software tools for primer design and sequence analysis. What Mynvax offers: A dynamic research environment with exposure to cutting-edge vaccine development. Mentoring by senior scientists and opportunity for career growth. Competitive salary and full-time employment benefits. Location: Bangalore, India Company: Mynvax Private Limited Position Type: Full-Time Start Date: Immediate How to Apply: Email your CV and a brief cover letter to careers@mynvax.com Subject line: "Application-Research Associate Molecular Biology" Apply on LinkedIn: Research Associate-Molecular Biology

Job Description: We are actively seeking ENM Outpatient (OP) and Inpatient (IP) Coders to join our growing team in the health and science sector. The ideal candidates will have a minimum of 1 year of experience specifically in E/M coding (OP or IP). This is a full-time, office-based role offering a dynamic work environment and opportunities for professional development. Industry: Health and Science Location: Work from Office Employment Type: Full-Time Salary: Up to 8LPA (Based on Experience) Key Responsibilities: Review and analyze medical records to assign accurate E/M codes for OP or IP services Ensure compliance with all applicable coding guidelines and regulations Maintain coding accuracy and productivity standards Work closely with the clinical and billing teams to resolve documentation and coding discrepancies Stay updated with the latest coding rules and healthcare guidelines Required Qualifications: Any Graduate (Bachelors degree in any discipline) Strong understanding of E/M coding practices Excellent attention to detail and analytical skills Good communication and organizational abilities Preferred Experience: Minimum 1 year of hands-on experience in ENM OP or ENM IP coding Experience working with electronic health records (EHR) systems and coding software Perks & Benefits: Competitive salary package (up to 8LPA) Professional growth and learning opportunities Supportive team culture Health and wellness support Interested candidates can share their portfolio/Resume To Whatsapp : 7842224022 Email: ramadevi.axisservices@gmail.com

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

We are Hiring For "Medical Coders"// up to 9 LPA // Certification is Mandatory Qualification: Any Degree Experience : Minimum 1 year relevant experience is mandatory 1. IPDRG Coder : Noida / Hyd / Chennai 2. Surgery Coder : Hyderabad / Chennai / Bangalore / Noida 3. Denials : Chennai / Hyderabad 4. Radiology : Chennai 5. ENM : Chennai / Bangalore 8. ED Blended : Hyderabad 9. Obgyn : Chennai 10. Enm with Surgery : Chennai Work from office / Relieving is mandatory Interested candidates can share your updated resume to HR sadhvika (9100163918) ( Via What's app ) sadhvika.axishr@gmail.com ( Via Mail ) Reference are welcome.

The Inpatient DRG Reviewer will be primarily responsible for conducting post-service, pre-payment and post pay comprehensive inpatient DRG reviews based on industry standard inpatient coding guidelines and rules, evidence based clinical criteria plan, and policy exclusions. Conduct reviews on inpatient DRG claims as they compare with medical records ICD-10 Official Coding Guidelines, AHA Coding Clinic and client specific coverage policies. Conduct prompt claim review to support internal inventory management to achieve greatest savings for clients. Please share relevant profiles at the earliest. Let us know if you need any further details. We are looking for professionals with strong expertise in DRG. The ideal candidates should have: Key Responsibilities: Perform comprehensive inpatient DRG validation reviews to determine accuracy of the DRG billed, based on industry standard coding guidelines and the clinical evidence supplied by the provider in the form of medical records such as physician notes, lab tests, images (x-rays etc.), and with due consideration to any applicable medical policies, medical best practice, etc. Based on the evidence presented in the medical records, determine, and record the appropriate (revised) Diagnosis Codes, Procedure Codes and Discharge Status Code applicable to the claim. Using the revised codes, regroup the claim using provided software to determine the new DRG’ Where the regrouped ‘new DRG’ differs from what was originally claimed by the provider, write a customer facing ‘rationale’ or ‘findings’ statement, highlighting the problems found and justifying the revised choices of new codes and DRG, based on the clinical evidence obtained during the review Document all aspect of audits including uploading all provider communications, clinical rationale, and/or financial research Identify new DRG coding concepts to expand the DRG product. Manage assigned claims and claim report, adhering to client turnaround time, and department Standard Operating Procedures Meet and/or exceed all internal and department productivity and quality standards Recommend new methods to improve departmental procedures Achieve and maintain personal production and savings quota Maintain awareness of and ensure adherence to Zelis standards regarding privacy Skills, Knowledge, and Experience: Registered Nurse licensure preferred Graduate Inpatient Coding Certification required (i.e., CCS, CIC, RHIA, RHIT) 3 – 5 years reviewing and/or auditing ICD-10 CM, MS-DRG and APR-DRG claims preferred Solid understanding of audit techniques, identification of revenue opportunities and financial negotiation with providers Experience and working knowledge of Health Insurance, Medicare guidelines and various healthcare programs Understanding of hospital coding and billing rules Clinical skills to evaluate appropriate Medical Record Coding Experience conducting root cause analysis and identifying solutions Strong organization skills with attention to detail Outstanding verbal and written communication skills Interested candidates can reach out through kavya.p- 8341137995

Greeting from Shrishaa HR Solutions! Candidates should have experience in Denial coding Minimum 2 Years of experience in medical Coding ( Along with ED/EM/Radiology/Surgery ) Work from Office Immediate joiners preferred Regards, Kalai HR 7904847280

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

Candidates should have experience in Denial coding Minimum 2 Years of experience in medical Coding ( Along with ED / EM / Radiology / Surgery ) Work from Office Looking for Immediate joiners preferred Regards, Krish 9342780488

SAP EHS Product Stewardship (PS) Functional Consultant – Digital Services ERM Digital Services is seeking a Functional Consultant in India to join our global practice. The successful candidate will have SAP EHS Product Stewardship / Product Compliance (PS) global regulatory, business process and technical solution design / implementation experience. They will be highly skilled in SAP EHS PS solution functionality supporting specification database data model design (hierarchy, compositions, inheritance, value assignment, etc.), safety data sheet authoring and distribution (SDS), label authoring and generation (GLM), hazardous materials / dangerous goods classification and shipping (DG) and global product compliance / substance volume tracking (SVT). Additional SAP EHS PS technical skills including Word for Windows (WWI) template building and management, third party specification data loading and management (OCC / ADM), expert rules configuration and management (Expert) and EHS PS infrastructure design, configuration and management including Generation server (GenPC) and Expert servers is highly desired. This position will assume a pivotal role in shaping a growing technology solutions practice, and will provide technology enabled global product stewardship / product compliance business process project delivery solutions and business process outsourcing (BPO) services including specification database maintenance and management, SDS authoring and distribution, WWI template management and system run and maintain support. As the SAP EHS PS Functional Consultant, you will be a valuable player amongst a diverse team of professionals that are fast-paced and streamlined to address business growth, daily business operations and product stewardship / compliance issues. The primary purpose of this role is to apply strong SAP functional and technical skills and EHS PS subject matter knowledge to effectively work with key clients by assisting them with their SAP implementations and SAP EHS platform based PS BPO services. It is both a hands-on role as well as leading and developing our SAP EHS PS capability in conjunction with the global PS DS lead partner and our global PS line of service. The ideal candidate brings significant consulting experience and client relationships that will provide leadership, strategic direction, BPO provision experience and cutting-edge SAP support to help grow ERM’s Digital Services business. RESPONSIBILITIES: Evaluate EHS PS software systems available on the market, including assisting clients with system requirements and system selection. Provide advice on different EHS PS software systems in response to specific data, organizational and operational requirements. Interact with clients on a routine basis to gather requirements and develop a full understanding of various business scenarios in order to assist with the development of appropriate proposals. Engage in all life cycle stages of project execution; provide support and enhancement to SAP platforms and solutions as required to meet the overall business objectives of clients. Lead development product stewardship / compliance business process outsourcing (BPO) solution center of excellence with focus on SAP platform and global SDS authoring and delivering. Providing leading role in conjunction with SAP PS DS global partner lead and global PS service line to develop PS BPO opportunities and provide service delivery staffing scale-up, engagement management and quality assurance. Identify and deliver solutions and integration services for SAP EHS PS functional areas using project management and business analysis methodologies on projects of diverse complexity and scope; implement requested enhancements with appropriate testing, change management and communication processes. Meet with customers to gather and document effective business requirements and translates requirements into blueprint and other system design documents. Facilitate management of change issues with the adoption of new information systems. Implement EHS PS software solutions such as SAP for clients worldwide. Assist with SAP system configuration, integration, training, rollout, support, maintenance, and improvements. Lead consultant teams that configure/deploy SAP EHS PS solutions; specific activities include publishing system design documents, configuring components within the solution, analyzing/migrating data, and developing custom reports/dashboards and automated interfaces. Support consultant teams that develop environmental solutions with drafting system design documents, configure technical specifications, analyze/migrate data, and develop automated custom reporting functionality. Demonstrate a thorough understanding of SAP methodology, principles, theories, concepts and techniques. Analyze user requirements, prepare requirements document, as-is & to-be processes and identify gaps. Design processes to meet requirements and prepare functional specifications. Collaborate with clients to develop/refine implementation strategy and on-going testing needs. Prepare test plans, conduct testing validation, and support user acceptance testing (UAT). Develop analytical reports and assist with documenting applications, data integration, and support procedures. Provide knowledge transfer enablement through formal documentation and end-user training. Engage in system support and training documentation teams, prepare and present training to internal consultants and client system users. Support pre-sales team on RFP preparation with the scope of work, timeline plan and high-level project plan. REQUIREMENTS: Bachelor’s degree in a technical field such as Information Technology, Computer Science, Engineering, or Management Information Systems. Strong chemistry and Product Stewardship / compliance knowledge and experience Experience with a minimum of three full life-cycle implementations including all phases such as planning, defining requirements, design, build, test, and deployment. Experience with product stewardship / compliance BPO services such as SDS authoring 5 to 10 years of relevant work experience in an EHS related field. Hands on experience with SAP EHS PS functional areas and business processes including Specification Management, SDS, GLM, DG and PC / SVT; demonstrated project delivery experience including implementation, development of test scripts, load testing, and working with technical and functional teams top perform analysis and make recommendations based on testing results. Hands on experience with unique SAP EHS PS infrastructure requirements (GenPC and Expert servers) and technical tools (WWI, OCC/ADM, Expert) Strong experience in SAP system development lifecycle from understanding of requirements to proper design technique, configuration, writing, specifications, testing, and documentation as needed. Diversified information technology experience and sound knowledge of EHS software, methodologies, domains and technology preferred. (Product Stewardship / Compliance: SDS, GLM, DG, PC/SVT) Ability and willingness to travel full time to client site if needed. Who We Are: As the world’s leading sustainability consulting firm, ERM is uniquely positioned to contribute to the environment and society through the expertise and energy of our employees worldwide. Sustainability is what we do, and is at the heart of both our service offerings and how we operate our business. For our people, our vision means attracting, inspiring, developing and rewarding our people to work with the best clients and on the biggest challenges, thus creating valuable careers. We achieve our vision in a sustainable manner by maintaining and living our ERM values that include Accountability, Caring for our People, Client Focus, Collaboration, Empowerment, and Transparency. ERM does not accept recruiting agency resumes. Please do not forward resumes to our jobs alias, ERM employees or any other company location. ERM is not responsible for any fees related to unsolicited resumes. ERM is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, gender, sexual orientation, gender identity, age, marital status or disability status. Thank you for your interest in ERM.