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Education and Work Experience Requirements: 4 to 6 years of experience as Data Scientist Proven track record and experience with statistical modeling/data mining algorithms such as Multivariate Regression, Logistic Regression, clustering algorithms, Support Vector Machines, Decision Trees etc Machine learning, deep learning, graph mining. DOE, Forecasting, Segmentation, Uncertainty Analysis etc. Data Mining i. e. Text Mining, Classification Methods SVM, NN, etc Vector Space model for Unstructured Text Sentiment Analysis, Association Mining, Semantic Analysis Good knowledge of advanced statistical methods. Experience working with Text Data using transformer-based model Experience in creating statistical models and/or optimization frameworks for improving processes/products/profits Expertise with one of the following scripting languages: Python, R, Tensorflow, Keras, Pytorch OpenNLP, CoreNLP, WordNet, NLTK, SpaCy, Gensim, Large Language Models, Knowledge Graphs Good and experience of machine learning algorithms and ability to apply them in supervised and un-supervised NLP tasks. Knowledge of NLP algorithms that can handle various NLP tasks such as intent recognition, entity extraction, language modeling, text classification, question answering, text summarization, topic modeling and so on. Experience building and fine-tuning Language Models (LMs), such as BERT, ELMo, XLNet etc to solve bespoke NLP tasks. Tech savy and willing to work with open-Source Tools Should have independently handled a project technically and provided directions to the other Team Members. Able to lead the project independently. Experience in turning ideas into actionable designs. Able to persuade stakeholders and champion effective techniques through development. Strong interpersonal and communication skills: ability to tell a clear, concise, actionable story with data, to folks across various levels of the company. Good to have foundational knowledge on Cloud, API frameworks like Flask, Fast API Prior experience working on Mobility or Healthcare domain will be a plus

Key Responsibilities: Oversee delivery operations for multispecialty coding teams. Ensure compliance with CPT, ICD-10, and HCPCS coding standards. Monitor productivity, quality, and SLA adherence across accounts. Collaborate with QA, Training, and Client Services to drive performance. Mentor Team Leads and Assistant Managers to build leadership capability. Implement process improvements and automation strategies. Handle client communications and reporting for operational updates. Qualifications: 12+ years of experience in US healthcare RCM, with strong expertise in multispecialty coding. CPC, CCS, or equivalent certification. Proven experience in managing large teams and client delivery. Strong analytical, communication, and stakeholder management skills. Bachelor's degree in Life Sciences or Healthcare; advanced degree preferred.

Experience Overall 4-8 Years & minimum 3 Years in SDS2 Modeling Roles and Responsibilities Perform detailed 3D modeling of structural steel using SDS2 software adhering to AISC standards Should have hands-on experience in SDS2 connection application and connection report extraction Must be familiar with AISC standard connections and Code standards Generation of technical queries and administration of same is preferred. Must have working ability in preparation and checking of fabrication drawings for all types of main structural members of all types of structures. Must be able to prepare and check G.A. & marking plans for all types of structures. Modelling and editing of miscellaneous items like handrails, stairs, safety gates & ladders and generating reports for cold rolled sections is mandatory. Interpretation, checking and incorporation of sub-trades details (e.g., flooring, decking, cladding etc.) into relevant models is desired. Should be able to read and understand the client design drawings and standards. Should be able to assume complete responsibility of ensuring the quality of model and drawings produced by self. Should be able to handle the changes, site works and revision of drawings. Should be hands-on in below areas: SDS2 modeling knowledge is mandatory Good Communication skills is mandatory Template setting and editing knowledge in preferred. Should be able to handle the project individually GA creation & editing TQ / RFI Preparation

Knovea Pharmaceutical Pvt. Ltd. is looking for talented professionals to join our Process Engineering (Mechanical) team in Indore, MP. Designation: AGM No. of openings: 1 Experience: 18 to 25 years Location: Indore, MP Industry: Pharmaceutical Manufacturing (Formulation injectable) Key Responsibilities: Review of equipment’s design qualification documents like PI&D, FS, DQ, SDS, HDS, IQ, OQ & drawings if applicable etc. and its approval if required. FAT to be done for the process equipment’s if required. Support shall be given to installation & commissioning activities. To support qualification activities for the equipment’s like IQ, OQ & PQ All the process equipment and utilities equipment’s shall be identified by the team and schedule shall be prepared for Maintenance. Approve the calibration vendor for third party calibrations. Review of calibration certificates and its approval if required. Coordination with the vendors Spares indents, QMS elements like change control, deviations etc. to be initiated and its approvals. To attend Equipment maintenances like preventive maintenance, breakdown etc. Preparation of SOP’s and its approvals. If you’re passionate about engineering excellence and innovation, we’d love to hear from you!

Location: Delhi/NCR Employment Type: Full-Time Experience Level: 3–7 Years Role Overview: We are seeking a skilled Automation Engineer with hands-on expertise in Allen-Bradley (RSLogix 5000, Studio 5000) and Siemens (TIA Portal, Step 7) PLC systems. The ideal candidate will be responsible for designing, programming, testing, and commissioning industrial automation solutions across diverse sectors. Key Responsibilities: Develop and implement PLC logic for AB and Siemens platforms Configure and integrate SCADA/HMI systems (FactoryTalk View, WinCC, etc.) Perform FAT/SAT , troubleshooting, and on-site commissioning Design control architectures and I/O mapping for automation projects Collaborate with cross-functional teams (mechanical, electrical, software) Prepare technical documentation: FDS, SDS, wiring diagrams, and test protocols Ensure compliance with SIL3 safety standards , GMP, and industry regulations Support AMC services and provide training to client teams Technical Skills Required: TechnologyProficiencyAB PLCs (RSLogix, Studio 5000)✅ RequiredSiemens PLCs (S7-300/400/1200/1500, TIA Portal)✅ RequiredSCADA/HMI (FactoryTalk, WinCC, Citect)✅ PreferredCommunication Protocols (EtherNet/IP, Profibus, Profinet)✅ RequiredElectrical Design Tools (AutoCAD, EPLAN)✅ PreferredSafety Systems (SIL2/SIL3)✅ Advantageous Qualifications: Bachelor’s degree in Electrical, Electronics, Instrumentation, or Mechatronics Engineering Minimum 3 years of experience in industrial automation projects Strong understanding of control system architecture and field instrumentation Soft Skills: Excellent problem-solving and analytical abilities Strong communication and documentation skills Willingness to travel for site commissioning and client support

Key Responsibilities: · Lead and manage QC operations for raw materials, in-process, and finished products. · Oversee analytical testing methods: HPLC, UV Spectrophotometer, Kjeldahl, KF Titrator, SDS-PAGE, Hydroxyproline test, Protein content analysis. · Review and approve COAs, protocols, and reports in compliance with GMP, ISO 13485, and 21 CFR Part 11. · Ensure calibration and preventive maintenance of QC instruments. · Train and mentor QC team to maintain accuracy, compliance, and data integrity. · Handle deviations, OOS/OOT investigations, and implement CAPA. · Ensure audit readiness and regulatory compliance at all times. · Prepare, review, and control QC documents (SOPs, protocols, reports, records). · Approve test protocols and reports; ensure proper record keeping. · Plan and utilize manpower, equipment, and consumables effectively. · Oversee method validation, verification, and transfer for chemical and microbiological tests. Qualifications & Experience: · M.Sc. (Chemistry / Biochemistry) or B.Pharm / M.Pharm. · 5-8 years of QC experience in pharmaceuticals / medical devices / biotech, · Strong knowledge of analytical techniques and regulatory requirements. · Experience in handling customer and regulatory audits preferred. Job Type: Full-time Pay: From ₹35,000.00 per month Benefits: Paid sick time Paid time off Experience: hr: 2 years (Preferred) HR sourcing: 1 year (Required) Language: English (Required) Work Location: In person

A Store Executive in the Chemical Industry typically oversees the management and operations of the warehouse, ensuring smooth handling of raw materials, chemicals, and finished goods. The role involves coordinating inventory control, storage, and distribution in compliance with safety standards and industry regulations. Here’s a detailed list of job responsibilities and qualifications that might be part of the position: Key Responsibilities: Inventory Management: Maintain and manage the inventory of chemicals and other warehouse materials. Regularly check stock levels and ensure timely replenishment of items. Implement efficient inventory control systems (e.g., FIFO, LIFO). Safety & Compliance: Ensure all safety protocols and regulations specific to chemical handling are strictly followed. Conduct safety audits and ensure compliance with environmental and safety standards (e.g., OSHA, ISO). Handle hazardous materials with care and ensure proper labeling and storage. Coordination: Coordinate with suppliers and transportation companies to ensure the timely arrival of shipments. Work closely with procurement and production departments to align inventory levels with demand. Documentation: Maintain accurate records of incoming and outgoing shipments, inventory levels, and warehouse transactions. Ensure proper documentation for chemical storage, including safety data sheets (SDS), and shipment tracking. Warehouse Operations: Supervise the loading and unloading of goods. Organize the layout of the warehouse to optimize space and material handling. Manage warehouse staff and ensure productivity targets are met.

Company Description 4XStruct takes pride in delivering exceptional services even under tight deadlines by utilizing a technology-driven approach. With over 20 years of experience in structural steel detailing, fabrication, branding, operations, and project management, our leadership and management team promotes distinctiveness, efficiency, and innovation. We invest in training to ensure our staff are equipped with the latest tools, techniques, and knowledge, allowing us to adapt effectively to evolving client needs. We view our workforce as a vital asset, which enhances client retention and stimulates business growth. Role Description This is a full-time on-site role for Tekla and SDS Experts, located in Nashik. The role involves creating detailed structural designs and fabrications using Tekla and SDS/2 software. The Tekla and SDS Experts will also be responsible for reviewing project specifications, collaborating with engineers and project managers, ensuring compliance with relevant codes and standards, and troubleshooting technical issues as they arise. Qualifications Proficiency in Tekla Structures and SDS/2 software Experience in structural steel detailing and fabrication Understanding of project specifications, codes, and standards Ability to collaborate with engineers and project managers Problem-solving and troubleshooting skills Detail-oriented with strong communication abilities Experience in on-site roles and willingness to work in Nashik Bachelor’s degree in Civil Engineering or related field is preferred

Looking for any Certified/Non-Certified Medical coder Coder/QA Surgery Coder/QA/SME IVR Coder/QA/SME EM Coder/QA/SME Anesthesia Coder/QA/SME Both Work From Home and Work From Office is available. Preferably Immediate Joinees or 30 days Required Candidate profile Looking for Certified/Non Certified Medical coder with any specialty like IVR/HHC Coder/QA Surgery Coder/QA/SME EM Coder/QA/SME Anesthesia Coder/QA/SME

Looking for any Certified/Non-Certified Medical coder HHC Coder/QA Radiology Coder/QA/SME IPDRG Coder/QA/SME HCC Coder/QA/SME Both Work From Home and Work From Office is available. Preferably Immediate Joinees or 30 days Required Candidate profile Looking for any Certified/Non-Certified Medical coder HHC Coder/QA Radiology Coder/QA/SME IPDRG Coder/QA/SME HCC Coder/QA/SME

( NOTE: FRESHERS NO OPENINGS ) WE'RE HIRING: >> Denial Certified (CHN /CBE/ PUNE) WFO And WFH Available >> EM Certified (CHN / PUNE) Chennai-WFH >> EM Non-Certified (CBE / PUNE)-Cross training Only WFO >> Surgery Certified (CHN /CBE / PUNE) WFO And WFH Available >> ED Facility Certified (CHN / PUNE) WFO And WFH Available Requirements : > Minimum 1+ year experience needed > Salary as per market standards > Only for certified coders > Relieving letter is not mandatory > Preferably Immediate > 10 days' notice period acceptable Freshers not eligible Salary as per Company norms Interview Mode : Virtual Work mode: WFO/WFH both available Contact: HR 9344964267 (Interested please share your resume to mentioned number) Refer and share with someone who might be a great fit!

Hiring Skilled Medical Coders Join Our Growing Team! Specialty: Same day Surgery (SDS) Experience: 1+ Years Key Skills : CPT & ICD-10-CM coding, endoscopy/EGD procedures, APC understanding, medical necessity checks Location : Chennai , Hyderabad,Coimbatore and Mumbai Certified / Non Certified Can Apply Salary: Best in Industry Mode of the Interview: Virtual Interview NP : Immediate joiner / 30days Apply Now / Share Referrals : 88259 26294 Whats App : 9003377697 Mail Id : harshini@smsjobs.in Fresher Not Eligible Don't miss this chance to level up your coding career

Computer System Validation Engineer Job Overview We are looking for an innovative and experienced Computer System Validation (CSV) Engineer to join our team. The CSV Engineer will be joining a quality team that is validating the quality of a new software/system. You will be responsible for oversight of all GxP regulated computerized systems at all applicable points of the computerized system lifecycle, ensuring compliance with regulatory requirements, Computer Systems Validation (CSV) and Lifecycle procedures with Data Integrity requirements. Experience 1-2 Years Responsibilities and Duties · Preparation and review of Validation deliverables such as URS, GxP, Impact Assessment Checklist, VP, Specification documents (SDS, FRS, TS, CS), FRA, IQ Protocol & Scripts, OQ Protocol & Scripts, PQ Protocol & Scripts, DM (Data Migration) Protocol & Scripts, RTM, VSR, 21 CFR PART 11 & EU ANNEX 11 Compliance Checklist as per Webosphere CSV SOP. · Execution/Support in the execution of IQ, OQ, PQ, and DM test scripts on the internal as well client side. · Basic knowledge of industry standards related to computerized systems and Electronic Records/Electronic Signatures; 21 CFR Part 11, EU Annex 11, GAMP5. · Coordinate with Client to carry out Validation activity of Computerized Systems and Software. · Responsible for achieving & maintaining the validated status of in-scope computerized systems · Provide guidance on CSV validation issues and discrepancies · Support investigation of CSV defects and quality records (deviation, CAPAs). · Ensuring systems are fully implemented and integrated with other quality management systems, site and global functions. · Coordinating with teammates in achieving assigned tasks. · Issue/bug tracking, and software incident management. · Develop and execute test plans to ensure that all objectives are met. · Implement and monitor test scripts to assess functionality, reliability, performance, and Coordinate and support to Quality Manager. · Ensure that user expectations are met during the testing process · Documentation adherence to internal/Client SOP and compliance. · Managing department functional process as specified in standard operation procedure & suggest changes if required. Qualifications · Past experience writing, reviewing and executing computer validation documentation (URS, GxP, VP, Specification documents, FRA, IQ, OQ, PQ, RTM, VSR, 21 CFR PART 11 & EU ANNEX 11 Compliance Checklist) · Excellent written and verbal communication skills. · Proficiency with MS Office tools · Documentation management · Ability to work as a team player in a consulting environment · Knowledge of Computer System Validation. · Critical thinker and creative mindset – and the ability to approach a problem creatively. · A meticulous approach to work. · A team player but can work independently too. · Multi-tasking and time-management skills, with the ability to prioritize tasks. Job Types: Full-time, Permanent Pay: Up to ₹420,000.00 per year Benefits: Health insurance Provident Fund Application Question(s): How soon you can join if get selected? As we are looking for immediate joiners only. what is your current location? (City) What is your current CTC? What is your expected CTC? Experience: Computer System Validation Engineer: 2 years (Required)

Roles & Responsibilities : 2 - 3 years of experience in SAP system Monitoring Monitor Java batch jobs and SAP Basis background jobs on a daily basis. Proactively identify job failures, delays, or performance issues and take corrective actions. Perform first-level troubleshooting (log analysis, reruns, dependency checks). Collaborate with SAP Basis administrators, Java developers, and functional teams for resolution. Conduct daily system health checks for SAP and Java environments. Ensure job completion within defined SLA timelines. Track, log, and report job failures; provide daily/weekly monitoring reports. Soft Skills: Good analytical and problem-solving skills. Good communication skills. Team collaboration and stakeholder interaction skills. Ability to manage multiple priorities and deadlines.

This job is with Organon, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Responsibilities Job Description Order to Cash (OtC) Management OtC Cycle Oversight: Manage the entire Order to Cash cycle, including customer order management, execution, and ensuring timely delivery of products to customers. Alliance Partners and SCM Governance: Collaborate with alliance partners to establish and maintain effective supply chain governance, ensuring compliance and alignment with strategic goals. Order Management: Coordinate order processing for all market customers, ensuring compliance with commercial and quality guidelines/SOPs. Inventory Control: Monitor inventory levels across super distributors (SDs) to prevent obsolescence and ensure product availability aligns with forecasts. Timely Shipment Delivery: Process, monitor, and deliver shipments to respective SDs/customers in a timely manner, maintaining high service levels (On-Time In-Full, Line-Item Fill Rate). Compliance Assurance: Ensure adherence to standard operating procedures (SOPs) and company policies throughout the OtC process, Including all ERP (Athena) transactions. Planning Process Management Demand Planning: Oversee demand planning for India and neighboring markets, ensuring accurate forecasts that align with business objectives. Fulfillment Planning: Manage fulfillment planning for local source supplies & review import supplies, optimizing supply chain efficiency. MRP Cycle Monitoring: Review the Material Requirements Planning (MRP) cycle, communicating net requirements to the respective import teams. Supply Chain Execution Management: Drive initiatives to monitor plan versus actuals, addressing chronic supply issues and updating stakeholders on constraints and potential sales losses. Collaboration with Regulatory : Collaborate with regulatory team to identify impacts on planning & supplies due to regulatory changes. Product Availability Monitoring: Ensure product availability aligns with forecasts at hubs. SD Management : Ensure product availability at Super distributors. Manage inventory across SDs while controlling inventory obsolescence. Key Deliverables Cost to Serve: Monitor and optimize the cost to serve metrics. Inventory Management: Analyze inventory norms based on product contributions and support improvements in inventory planning. Service Levels: Maintain high service levels and ensure compliance metrics are met. Forecast accuracy , On-Time In-Full, Line-Item Fill Rate) Relationship Management Organizational Development: Build and lead a highly effective supply chain organization capable of cross-functional collaboration. Stakeholder Engagement: Cultivate strong relationships with internal and external stakeholders to continuously understand and meet customer requirements. Required Education, Experience And Skills Graduate in Engineering or Supply Chain-related fields. A Master's degree is an added advantage. Experience in Supply Chain (Order to Cash, Planning Process, and Alliance Management). SAP experience 2-8 years - MM Module Secondary Job Description Who We Are: Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women's Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman. As an equal opportunity employer, we welcome applications from candidates with a diverse background. We are committed to creating an inclusive environment for all our applicants. Search Firm Representatives Please Read Carefully Organon LLC, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Annualized Salary Range Annualized Salary Range (Global) Annualized Salary Range (Canada) Please Note: Pay ranges are specific to local market and therefore vary from country to country. Employee Status Regular Relocation: No relocation VISA Sponsorship Travel Requirements: Organon employees must be able to satisfy all applicable travel and credentialing requirements, including associated vaccination prerequisites Shift Flexible Work Arrangements: Valid Driving License Hazardous Material(s): Number Of Openings 1 Requisition ID: R534498

Title of the position: Logistics Specialist (Manger) Location: TSMPL-Dholera, Gujarat About The Business Tata Electronics Private Limited is a prominent global player in the electronics manufacturing industry, with fast-emerging capabilities in Electronics Manufacturing Services, Semiconductor Assembly & Test, Semiconductor Foundry, and Design Services. Established in 2020 as a greenfield venture of the Tata Group, the company aims to serve global customers through integrated offerings across a trusted electronics and semiconductor value chain. With a rapidly growing workforce, the company currently employs over 65,000 people and has significant operations in Gujarat, Assam, Tamil Nadu, and Karnataka, India. Tata Electronics is committed to creating a socioeconomic footprint by employing many women in its workforce and actively supporting local communities through initiatives in environment, education, healthcare, sports and livelihood. Responsibilities Job Summary / Objective: This role involves managing and overseeing the end-to-end import, export, in Land transport and Logistics processes for Sensitive Semiconductor Equipments, ODC Cargo, Utilities, Gas, Chemicals, other direct/Indirect materials and Finished Goods Products, ensuring seamless operations, regulations enforced by various government bodies, classification (especially HTS, UN and CAS Number, SDS), cost-effectiveness, and strict compliance with all relevant Indian and international trade laws, IATA DGR, customs regulations, and safety standards, particularly those pertaining to hazardous materials. The specialist coordinates activities between suppliers, customers, logistics partners (like freight forwarders and Customs House Agents - CHAs), licensing authorities and regulatory bodies. Essential Attributes Establish logistics processes for Inbound and Outbound Semiconductor Equipment's, Utilities, Gas, Chemicals, other direct/Indirect materials and Finished Goods Products transportation from all global and domestic locations suppliers and customers. Plan, coordinate, and monitor inbound and outbound logistics activities. Manage transportation, and logistics across multiple 3PL sites (Internal and External warehouses), ensuring timely and accurate product delivery. Identify potential risks in the supply chain, such as transportation delays, supply disruptions, or natural disasters. Possessing a strong understanding of Indian regulations concerning import and export, as well as the storage and distribution of gases and chemicals. This includes knowledge of the Manufacture, Storage and Import of Hazardous Chemicals guidelines, IATA Regulations, Bureau of Indian Standards (BIS) certification, BIS certification under specific Quality Control Orders (QCOs), regulations from Pollution Control Boards, and PESO regulations. Analyse logistics workflows and KPIs to identify and implement cost-saving and process improvement initiatives Manage Reverse Logistics. Qualifications A preferred Bachelor's degree in Engineering or an equivalent field is advantageous, along with experience in Logistics and supply chain management field. Desired Experience Level Experience: Minimum of 12-14 years of proven experience in import/export operations, preferably within manufacturing sectors. Experience specifically in the Semiconductor Industry is a plus. Experience in Greenfield project is a plus. Regulatory Knowledge: Extensive knowledge of ODC Cargo, gas and chemical logistics, including Indian import and export regulations (Customs, DGFT, PESO, PCB), international trade laws, Incoterms, and compliance requirements, particularly for hazardous materials (HAZMAT). Logistics & Supply Chain Management: Strong understanding of International Logistic, 3PL Management, Inbound/Outbound logistics, multi-modal transportation, freight forwarding. Negotiation & Communication: Excellent verbal and written communication skills for liaising with diverse stakeholders globally and negotiating effectively. IT Proficiency: Competence in using MS Office Suite (Word, Excel), ERP systems (e.g., SAP), and potentially specific logistics/trade compliance software (e.g. TMS )

We are currently seeking an Assistant Manager ED/EM Medical Coding at Vee Healthtek. Job Description: - Must have over 8 years of experience in Medical Coding - Specialization in ED/EM Medical Coding - Experience of 8+ years on ED/EM - Designation: Assistant Manager/TL - Location: Pune (Work from office) Candidates must have experience in team handling, with a minimum of 3 years in team management, excellent communication skills, and client management abilities. Interested candidates are encouraged to contact us immediately at 9443238706 (also available on Whatsapp) or send your profile to ramesh.m@veehealthtek.com. Best Regards, Ramesh HRD Vee Healthtek

Role & responsibilities Job Title: Senior Manager Quality (Medical Coding) / Manager / Assistant Manager Experience Required: If anyone interested to work for Quality from Operations can also apply Senior Manager - 12+ Years in Medical Coding (with minimum 1 Year as Manager / Sr. Manager on papers) Manager -- 10+ years in Medical Coding (with minimum 1 Year as Manager/2 yrs as Assistant Manager on papers) Assistant Manager - 7+ years in Medical Coding (with minimum 1 Year as Assistant Manager/2 yrs as Team Lead on papers) Job Location: Hyderabad / Mumbai / Aurangabad Specialties: Hyderabad: IP DRG --Senior Manager Quality / Manager / Assistant Manager Quality Mumbai: Surgery, Anaesthesia, Home Health & HCC -- --Senior Manager Quality Aurangabad: Surgery, Anaesthesia, Home Health & HCC -- --Senior Manager Quality Key Skills: Medical Coding Quality, Coding Operations, DRG, Surgery Coding, Anaesthesia Coding, Team Management, Quality Audits, Compliance Compensation: Up to 32 LPA (based on experience) -- Senior Manager Up to 24 LPA (based on experience) -- Manager Up to 20 LPA (based on experience) -- Assistant Manager Notice Period: 0 to 60 Days Interested candidates can share their resumes with HR Surya - 8125761519 Preferred candidate profile

Job Title: Senior Manager Quality (Medical Coding) Experience Required: 12+ Years in Medical Coding (with minimum 1 Year as Manager / Sr. Manager on papers) Job Location: Hyderabad / Mumbai / Aurangabad Specialties: Hyderabad: IP DRG Mumbai: Surgery, Anaesthesia, IP DRG Aurangabad: Surgery, Anaesthesia Key Skills: Medical Coding Quality, Coding Operations, DRG, Surgery Coding, Anaesthesia Coding, Team Management, Quality Audits, Compliance Compensation: Up to 32 LPA (based on experience) Notice Period: 060 Days Interested candidates can share their resumes with HR Suvarna – 7095162832

Worldsource Healthcare India Job Title: Medical Coding Team Lead (Multi-Specialty & Emergency Department) Location: Chennai Department: Medical Coding Job Type: Full-Time Experience Level: Senior / Team Lead Job Summary: We are seeking a highly skilled and experienced Medical Coding Team Lead with extensive knowledge in multi-specialty coding and Emergency Department (ED) coding. The ideal candidate will have strong leadership capabilities, expertise in CPT, ICD-10-CM, and HCPCS coding systems, and a proven track record of team management in a healthcare setting. This role is responsible for supervising coders, ensuring quality and compliance, conducting audits, and maintaining productivity targets. Key Responsibilities: Lead and supervise a team of medical coders across multi-specialty domains including ED, Internal Medicine, Radiology, Cardiology, General Surgery, Orthopedics, and more. Assign work to the team and monitor coding queues to ensure timely completion of charts. Ensure coding accuracy and adherence to CMS guidelines, payer-specific rules, and organizational policies. Perform quality checks and internal audits to maintain high coding accuracy (typically 95%+). Provide training and mentorship to coding staff, including updates on coding guidelines and changes in regulations. Collaborate with Clinical Documentation Improvement (CDI), billing, and compliance teams to resolve coding discrepancies and denials. Monitor team productivity and performance metrics; report on KPIs to leadership. Stay updated with current coding trends, payer updates, and compliance standards. Handle escalations from team members or clients related to coding disputes or clarifications. Participate in hiring, onboarding, and performance evaluations of coding team members. Required Qualifications: Proficiency in ICD-10-CM, CPT, HCPCS Level II coding systems. In-depth knowledge of CPT Evaluation & Management (E/M) coding guidelines. Familiarity with NCCI edits, MUEs, and payer-specific coding requirements. Certifications (Required): CPC (Certified Professional Coder) AAPC or CCS (Certified Coding Specialist) AHIMA (Additional specialty certifications like CEDC, COC, or CIC are a plus) Preferred Skills: Experience with coding platforms such as 3M, EncoderPro, Optum360, Epic, Cerner, or similar. Strong communication, leadership, and interpersonal skills. Audit experience or background in compliance is a plus Preferred candidate profile Minimum 5+ years of experience in medical coding, with at least 2+ years in a leadership or supervisory role. Strong experience in multi-specialty and ED coding (facility and/or professional). Send Resume: skrishnamurthy@worldsourceteam.co.in Contact: 7397744009 Worldsource Healthcare India Pvt., Ltd., #16, RAJIV GANDHI SALAI, 4TH FLOOR WEST WING / BLOCK II, OMR KARAPAKKAM, CHENNAI - 600097.

We are looking for a skilled and experienced BIM Engineer Steel with a strong background in steel detailing and 3D modeling for structural steel projects across the UK, Europe, and the US. The ideal candidate will have hands-on expertise in Tekla Structures, Advance Steel, and AutoCAD, and should be well-versed in British and international steel detailing codes and standards (BS, Eurocodes, AISC, etc.). This role requires precision, discipline knowledge, and a collaborative mindset to deliver high-quality steel models, fabrication drawings, and coordinated outputs for global projects. We are committed to providing a supportive and adaptable work environment that encourages collaboration, innovation, and a healthy work-life balance. This role offers the flexibility to work in a hybrid or remote arrangement, depending on individual preferences and business needs. Roles and Responsibilities Create detailed and accurate 3D structural steel models using Tekla Structures and/or Advance Steel based on design documentation. Produce fabrication and erection drawings, GA drawings, material take-offs, and bolt lists per project specifications. Ensure strict compliance with regional standards including British Standards (BS), Eurocodes, and US standards (AISC). Interpret and translate architectural and structural drawings into coordinated steel models. Perform clash detection and interface coordination using BIM tools (e.g., Navisworks). Generate and manage Bills of Materials (BOMs), part lists, and production-ready deliverables aligned with fabrication and erection sequences. Work collaboratively with engineers, architects, and project stakeholders to resolve design or constructability issues. Maintain proper documentation, version control, and adherence to company BIM and QA/QC standards. Support coordination meetings and provide technical input for steel design integration. Necessary Requirement Bachelors degree in Civil Engineering with 3 to 6 years of relevant experience, OR Diploma in Civil Engineering with 9 to12 years of hands-on detailing experience. Proficiency in Tekla Structures (mandatory) and Advance Steel (preferred). Strong working knowledge of AutoCAD and general BIM workflows. Proven experience on UK, Europe, and/or US-based steel projects is essential. Deep understanding of British (BS), European (Eurocodes), and American (AISC) structural steel standards. Ability to interpret structural and architectural drawings and translate them into fabrication-ready models and drawings. Detail-oriented with excellent organizational, communication, and collaboration skills. Ability to work independently or as part of a remote/international team in a dynamic project environment. Preferred Experience Experience in BIM-based coordination for industrial, commercial, or infrastructure projects. Familiarity with fabrication workflows, connection detailing, and erection sequencing. Exposure to model-based delivery platforms such as BIM 360, Navisworks, or similar tools. Company Benefits Innovative & Evolving Work & People culture Competitive Work Benefits Outstanding Career growth opportunities Exposure to International Projects Everest Technical Services is proud to be an equal opportunities employer!

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

Position - Computer System Validation (CSV) Engineer Salary - 4.2LPA Experience - 1-2 Years Location - Ahmedabad, Gujarat Contact person : 9783222277 Working Days - Monday to Friday, 9:30AM to 7:00PM We are looking for an innovative and experienced Computer System Validation (CSV) Engineer to join our team. The CSV Engineer will be joining a quality team that is validating the quality of a new software/system. You will be responsible for oversight of all GxP regulated computerized systems at all applicable points of the computerized system lifecycle, ensuring compliance with regulatory requirements, Computer Systems Validation (CSV) and Lifecycle procedures with Data Integrity requirements. Responsibilities and Duties - Preparation and review of Validation deliverables such as URS, GxP, Impact Assessment Checklist, VP, Specification documents (SDS, FRS, TS, CS), FRA, IQ Protocol & Scripts, OQ Protocol & Scripts, PQ Protocol & Scripts, DM (Data Migration) Protocol & Scripts, RTM, VSR, 21 CFR PART 11 & EU ANNEX 11 Compliance Checklist as per Webosphere CSV SOP. Execution/Support in the execution of IQ, OQ, PQ, and DM test scripts on the internal as well client side. Basic knowledge of industry standards related to computerized systems and Electronic Records/Electronic Signatures; 21 CFR Part 11, EU Annex 11, GAMP5. Coordinate with Client to carry out Validation activity of Computerized Systems and Software. Responsible for achieving & maintaining the validated status of in-scope computerized systems Provide guidance on CSV validation issues and discrepancies Support investigation of CSV defects and quality records (deviation, CAPAs). Ensuring systems are fully implemented and integrated with other quality management systems, site and global functions. Coordinating with teammates in achieving assigned tasks. Issue/bug tracking, and software incident management. Develop and execute test plans to ensure that all objectives are met. Implement and monitor test scripts to assess functionality, reliability, performance, and Coordinate and support to Quality Manager. Ensure that user expectations are met during the testing process Documentation adherence to internal/Client SOP and compliance. Managing department functional process as specified in standard operation procedure & suggest changes if required. Qualifications - Past experience writing, reviewing and executing computer validation documentation (URS, GxP, VP, Specification documents, FRA, IQ, OQ, PQ, RTM, VSR, 21 CFR PART 11 & EU ANNEX 11 Compliance Checklist) Excellent written and verbal communication skills. Proficiency with MS Office tools Documentation management Ability to work as a team player in a consulting environment Knowledge of Computer System Validation. Critical thinker and creative mindset – and the ability to approach a problem creatively. A meticulous approach to work. A team player but can work independently too. Multi-tasking and time-management skills, with the ability to prioritize tasks. Job Types: Full-time, Permanent Pay: Up to ₹420,000.00 per year Benefits: Health insurance Provident Fund Application Question(s): What is your current and expected CTC? Experience: Computer System Validation: 2 years (Preferred) Work Location: In person

About the Job: Reprosci Biosciences Private Limited is actively engaged in developing regenerative therapies in reproductive medicine, with a focus on autologous biologics such as PRP-derived exosomes. In collaboration with the Center for Translational Research in Reproductive Health, PSG Institute of Advanced Studies, we conduct cutting-edge research involving bioformulation, cell-based assays, exosome isolation and characterization, and in-vitro functional studies targeting endometrial regeneration. Our R&D aims to bridge lab-scale innovation and clinical translation, emphasizing personalized, non-hormonal fertility therapeutics. Ongoing activities include product optimization, preclinical validation, and preparation for regulatory submissions. About the Role: We are seeking a highly motivated and skilled Senior Research Scientist to join our team, driving innovation in regenerative medicine, stem cell therapy, and next-generation biotechnology platforms. The ideal candidate will lead research in cell culture, molecular biology, and advanced regenerative modalities, guiding a talented team toward impactful scientific and translational outcomes. What You’ll Do: Lead cell culture and molecular biology experiments, ensuring best practices in mammalian cell culture technologies and laboratory maintenance. Work with stable and transient transfections for recombinant protein/antibody expression across various mammalian cell lines (CHO, HEK, etc.). Design, execute, and troubleshoot complex cell culture, transfection, and cell line generation projects. Develop and perform a wide range of assays (cell-free, cell-based, cytotoxicity, biochemical, microscopy, flow cytometry, western blot, ELISA, high-throughput screening, etc.). Support experiments using molecular biology techniques, including DNA/RNA extraction, PCR, qPCR, gel electrophoresis, and related analysis. Supervise and mentor Research Assistants and Lab Technicians with clear weekly and monthly milestones. Prepare presentations, posters, study reports, government grant proposals, and manuscripts for publication. Manage lab operations, including ordering, inventory, and regulatory compliance. Explore and integrate futuristic areas including Exosomes, 3D Bioprinting, and advanced Stem Cell technologies into ongoing and upcoming projects. What We’re Looking For: PhD in Molecular Biology, Cell Biology, Biotechnology, Biochemistry, or a related field. Strong knowledge of biochemistry and molecular biology principles and methodologies. Proven experience with mammalian cell culture, molecular biology techniques, PCR, ELISA, SDS-PAGE, Western blot, enzyme assays, and chromatography. Demonstrated leadership, organizational, and multitasking skills with attention to detail and strong record-keeping practices. Excellent communication and teamwork skills. Why Join Us: At ReprOsci , you'll be part of a passionate team at the forefront of regenerative medicine, working to translate breakthrough science into life-changing therapies. We offer a collaborative, innovation-driven environment where your ideas matter, your expertise shapes next-generation solutions, and your work directly contributes to addressing unmet clinical needs in reproductive health. With access to cutting-edge technologies, strategic academic collaborations, and a culture that values both scientific rigor and creative problem-solving, this is a unique opportunity to grow your career while making a tangible impact on the future of fertility therapeutics.

Position - Computer System Validation (CSV) Engineer Salary - 4.2LPA Experience - 1-2 Years Location - Ahmedabad, Gujarat Contact person : 9783222277 Working Days - Monday to Friday, 9:30AM to 7:00PM We are looking for an innovative and experienced Computer System Validation (CSV) Engineer to join our team. The CSV Engineer will be joining a quality team that is validating the quality of a new software/system. You will be responsible for oversight of all GxP regulated computerized systems at all applicable points of the computerized system lifecycle, ensuring compliance with regulatory requirements, Computer Systems Validation (CSV) and Lifecycle procedures with Data Integrity requirements. Responsibilities and Duties - Preparation and review of Validation deliverables such as URS, GxP, Impact Assessment Checklist, VP, Specification documents (SDS, FRS, TS, CS), FRA, IQ Protocol & Scripts, OQ Protocol & Scripts, PQ Protocol & Scripts, DM (Data Migration) Protocol & Scripts, RTM, VSR, 21 CFR PART 11 & EU ANNEX 11 Compliance Checklist as per Webosphere CSV SOP. Execution/Support in the execution of IQ, OQ, PQ, and DM test scripts on the internal as well client side. Basic knowledge of industry standards related to computerized systems and Electronic Records/Electronic Signatures; 21 CFR Part 11, EU Annex 11, GAMP5. Coordinate with Client to carry out Validation activity of Computerized Systems and Software. Responsible for achieving & maintaining the validated status of in-scope computerized systems Provide guidance on CSV validation issues and discrepancies Support investigation of CSV defects and quality records (deviation, CAPAs). Ensuring systems are fully implemented and integrated with other quality management systems, site and global functions. Coordinating with teammates in achieving assigned tasks. Issue/bug tracking, and software incident management. Develop and execute test plans to ensure that all objectives are met. Implement and monitor test scripts to assess functionality, reliability, performance, and Coordinate and support to Quality Manager. Ensure that user expectations are met during the testing process Documentation adherence to internal/Client SOP and compliance. Managing department functional process as specified in standard operation procedure & suggest changes if required. Qualifications - Past experience writing, reviewing and executing computer validation documentation (URS, GxP, VP, Specification documents, FRA, IQ, OQ, PQ, RTM, VSR, 21 CFR PART 11 & EU ANNEX 11 Compliance Checklist) Excellent written and verbal communication skills. Proficiency with MS Office tools Documentation management Ability to work as a team player in a consulting environment Knowledge of Computer System Validation. Critical thinker and creative mindset – and the ability to approach a problem creatively. A meticulous approach to work. A team player but can work independently too. Multi-tasking and time-management skills, with the ability to prioritize tasks. Job Types: Full-time, Permanent Pay: Up to ₹420,000.00 per year Benefits: Health insurance Provident Fund Application Question(s): What is your current and expected CTC? Experience: Computer System Validation: 2 years (Preferred) Work Location: In person