449 Sds Jobs - Page 5

Roles and Responsibilities Accurately code medical records using CPT, ICD-10, and HCPCS codes. Conduct IVR testing and SDS (Systems Development Survey) certification as required. Ensure compliance with regulatory guidelines and industry standards for medical coding. Collaborate with healthcare providers to resolve any discrepancies or issues related to coding. Maintain confidentiality and adhere to HIPAA regulations.

Business Analyst Requirements The SDS Business Analyst will be responsible for management of supplemental data sources (SDS), including audit documentation, HEDIS technical specification review, and tracking of supplemental data sources. This role requires collaboration with appropriate areas of the business to ensure the most efficient management of data with the highest level of quality and greatest Enterprise gain. All work supports Commercial, Medicare & Medicaid lines of business. Additionally, this role will support process improvement through the identification of data source opportunities for improvement and development of associated action plans. Primary Responsibilities: Source Management  Knowledgeable of clinical supplemental data sources as used in HEDIS® data processing - purpose, intent of use, data collection method  Responsible for audit documentation completion and quality of documentation  Responsible for medical record requests to support medical record review or primary source verification - related to HEDIS® audit  Knowledgeable of NCQA HEDIS® technical specifications regarding supplemental data and applicable measures  Responsible for tracking of source documentation readiness Data Management  Maintain documentation of end-to-end data flow of sources  Knowledgeable of data validation reports of sources  Awareness of data load specifications to HEDIS® rules engines Audit Management  Maintain documentation of audit review outcome by source  Support Quality Solutions Delivery with HEDIS® audit - for all audit groups involved with annual audit -- address audit issues/concerns within required turnaround time  Complete work on time, especially as it pertains to HEDIS® audit deadlines Other Responsibilities:  Develop & produce ad-hoc reports  Participate with complex analyses and reports  Works independently; seeks guidance on only the most complex tasks Show more Show less

Business Analyst Requirements The SDS Business Analyst will be responsible for management of supplemental data sources (SDS), including audit documentation, HEDIS technical specification review, and tracking of supplemental data sources. This role requires collaboration with appropriate areas of the business to ensure the most efficient management of data with the highest level of quality and greatest Enterprise gain. All work supports Commercial, Medicare & Medicaid lines of business. Additionally, this role will support process improvement through the identification of data source opportunities for improvement and development of associated action plans. Primary Responsibilities: Source Management  Knowledgeable of clinical supplemental data sources as used in HEDIS® data processing - purpose, intent of use, data collection method  Responsible for audit documentation completion and quality of documentation  Responsible for medical record requests to support medical record review or primary source verification - related to HEDIS® audit  Knowledgeable of NCQA HEDIS® technical specifications regarding supplemental data and applicable measures  Responsible for tracking of source documentation readiness Data Management  Maintain documentation of end-to-end data flow of sources  Knowledgeable of data validation reports of sources  Awareness of data load specifications to HEDIS® rules engines Audit Management  Maintain documentation of audit review outcome by source  Support Quality Solutions Delivery with HEDIS® audit - for all audit groups involved with annual audit -- address audit issues/concerns within required turnaround time  Complete work on time, especially as it pertains to HEDIS® audit deadlines Other Responsibilities:  Develop & produce ad-hoc reports  Participate with complex analyses and reports  Works independently; seeks guidance on only the most complex tasks Show more Show less

Role & responsibilities We are Hiring For "Medical Coders" Certification is Mandatory / Qualification: Any Degree CODERS : Minimum 1 year relevant experience is mandatory 1. IPDRG Coder : Noida / Hyd / Chennai / Mumbai || CTc up to 13 LPA || 2. Surgery Coder : Hyderabad / Chennai || CTc up to 10 lpa || 3. Denials : Chennai / Hyderabad|| CTc up to 10 lpa || 4. Radiology : Chennai / Trichy / bangalore || up to 48k Take home || 5. Anesthesia : Hyderabad || take home up to 48k || 6. ED Profee: Chennai / Bangalore || take home up to 48k || QUALITY ANALYST: Min 4 years as a Coder and 1 year exp as QA on (Or) off paper 1. Surgery : Hyderabad/ Chennai / Bangalore || take home up to 60k || 2. EM IP : Chennai , Bangalore || take home up to 60k || 3. IP drg : Hyderabad || CTC up to 12lpa || 4. EM Op : Bangalore , chennai || take home up to 60k || 5. Anesthesia : Hyderabad || take home up to 60k || PROCESS COACH: Min 4 years as a Coder and 1 year exp as QA on (Or) off paper 1. SDS : Bangalore , Chennai || CTC Up to 9LPA || 2. EM : Bangalore , Chennai || CTC Up to 9LPA || TEAM LEAD: Min 6 years exp as coder with exp 1 year (on papers) team lead 1. SDS : Bangalore , Chennai || CTC Up to 12LPA || 2. Home Health : Bangalore || CTC Up to 12 LPA || 3. EM : Bangalore , Chennai || CTC Up to 12 LPA || Work from office / Relieving is mandatory Interested candidates can share your updated resume to HR Pravalika 9100248649 (Via What's app) Preferred candidate profile

Business Analyst Requirements The SDS Business Analyst will be responsible for management of supplemental data sources (SDS), including audit documentation, HEDIS technical specification review, and tracking of supplemental data sources. This role requires collaboration with appropriate areas of the business to ensure the most efficient management of data with the highest level of quality and greatest Enterprise gain. All work supports Commercial, Medicare & Medicaid lines of business. Additionally, this role will support process improvement through the identification of data source opportunities for improvement and development of associated action plans. Primary Responsibilities: Source Management  Knowledgeable of clinical supplemental data sources as used in HEDIS® data processing - purpose, intent of use, data collection method  Responsible for audit documentation completion and quality of documentation  Responsible for medical record requests to support medical record review or primary source verification - related to HEDIS® audit  Knowledgeable of NCQA HEDIS® technical specifications regarding supplemental data and applicable measures  Responsible for tracking of source documentation readiness Data Management  Maintain documentation of end-to-end data flow of sources  Knowledgeable of data validation reports of sources  Awareness of data load specifications to HEDIS® rules engines Audit Management  Maintain documentation of audit review outcome by source  Support Quality Solutions Delivery with HEDIS® audit - for all audit groups involved with annual audit -- address audit issues/concerns within required turnaround time  Complete work on time, especially as it pertains to HEDIS® audit deadlines Other Responsibilities:  Develop & produce ad-hoc reports  Participate with complex analyses and reports  Works independently; seeks guidance on only the most complex tasks Show more Show less

Business Analyst Requirements The SDS Business Analyst will be responsible for management of supplemental data sources (SDS), including audit documentation, HEDIS technical specification review, and tracking of supplemental data sources. This role requires collaboration with appropriate areas of the business to ensure the most efficient management of data with the highest level of quality and greatest Enterprise gain. All work supports Commercial, Medicare & Medicaid lines of business. Additionally, this role will support process improvement through the identification of data source opportunities for improvement and development of associated action plans. Primary Responsibilities: Source Management  Knowledgeable of clinical supplemental data sources as used in HEDIS® data processing - purpose, intent of use, data collection method  Responsible for audit documentation completion and quality of documentation  Responsible for medical record requests to support medical record review or primary source verification - related to HEDIS® audit  Knowledgeable of NCQA HEDIS® technical specifications regarding supplemental data and applicable measures  Responsible for tracking of source documentation readiness Data Management  Maintain documentation of end-to-end data flow of sources  Knowledgeable of data validation reports of sources  Awareness of data load specifications to HEDIS® rules engines Audit Management  Maintain documentation of audit review outcome by source  Support Quality Solutions Delivery with HEDIS® audit - for all audit groups involved with annual audit -- address audit issues/concerns within required turnaround time  Complete work on time, especially as it pertains to HEDIS® audit deadlines Other Responsibilities:  Develop & produce ad-hoc reports  Participate with complex analyses and reports  Works independently; seeks guidance on only the most complex tasks Show more Show less

Position Summary: We are seeking a highly motivated and experienced Export Manager to lead and expand our international market presence in the agrochemicals sector, biologicals & biofertilizers. The ideal candidate will have a proven track record in international sales, a strong understanding of agricultural inputs (especially pesticides, herbicides, fungicides, biologicals & biofertilizers) & logistics. Key Responsibilities: International Market Expansion: Identify and evaluate new business opportunities in target geographies such as Middle East, Africa, Southeast Asia, South America and Europe. Build and develop a distributor network and strategic alliances with local partners, importers, and agri-cooperatives. Conduct market research and competitor analysis to tailor market entry strategies. Sales & Revenue Generation: Achieve sales targets and drive revenue growth across designated export regions. Meet and exceed export sales targets and KPIs across defined international territories. Manage pricing, margin analysis, and contract negotiations with international partners. Negotiate contracts, pricing structures, and commercial terms with clients and distributors. Supply Chain & Logistics: Oversee export logistics including documentation (LC, Bill of Lading, COO, SDS, etc.), shipping schedules, and customs clearance. Liaise with freight forwarders, warehouses, and third-party logistics providers to ensure timely and cost-effective deliveries. Client Relationship Management: Build and maintain long-term relationships with key customers and stakeholders. Provide after-sales support and handle any client issues or inquiries. Reporting & Strategy: Prepare regular sales reports, forecasts, and market intelligence briefs for senior management. Contribute to the development of the international business strategy and annual operating plan. Qualifications & Experience: Bachelor's or master's degree in agriculture, International Business, or a related field. Minimum 5–8 years of relevant experience in developing new markets in export sales of agrochemical, biologicals & biofertilizers products in Middle East, Africa, Southeast Asia, South America and Europe. Strong negotiation, communication, and interpersonal skills. Willingness to travel internationally as required. Job Type: Full-time Pay: ₹90,000.00 - ₹1,100,000.00 per month Benefits: Cell phone reimbursement Provident Fund Schedule: Fixed shift Morning shift Work Location: In person

Overview: Job Title: RA Assistant Location: Chennai Objective: The Regulatory Affairs (RA) Assistant is responsible for supporting the regulatory compliance efforts within the region. This involves ensuring adherence to local and international regulatory standards, assisting with product registrations, maintaining documentation, and liaising with regulatory agencies. The RA Assistant plays a key role in helping the business meet compliance requirements and facilitates a smooth regulatory process. The role also provides administrative and operational support to the Regulatory Affairs team for smooth functioning Responsibilities: Regulatory Compliance and Documentation Management: Maintain accurate knowledge of local regulatory requirements and ensure product compliance with national and/or international regulations. Develop and finalize product labels in alignment with country-specific requirements and oversee approval and production processes for India manufacturing. Create and maintain primary standard documents (including product specification, SDS, label, etc.) Support on BOM, variant and sample code creation. Regulatory Registrations, Stakeholder Liaison and Communication: Assist in preparing documents for product registrations dossier, imports and exports and custom clearance. Support the preparation of bi-annual reports such as heavy metal analyses for submission to FSSAI. Assist Manage FSSAI Manufacturing, Import, and Export Licenses for KFT products. Act as a liaison with regulatory officials, internally and externally, to ensure smooth information exchange in India. Support customer questionnaires, vendor registrations, and other regulatory or compliance tasks as needed. Audit and Training Support: Participate/support in internal audits and certifications renewal (E.g.: FOSTAC, HALAL, FSSC22000, etc.) Project Involvement: Support on PTP, PRI, PIP, or any other initiatives under the guidance of the Manager. Conduct research to support regulatory strategies and processes. Qualifications: Bachelor's or Master’s degree in Food Science, Chemistry, or a related field with 1-2 years of expereince . Preferably with knowledge of regulatory aspects in the food industry. #LI-SS1

Job Location : Kolkata Position : Company Secretary Experience : min 7 years post company secretary qualification Qualifications : Graduate with Company Secretary Industry : Joining : As soon as possible Skills : Good in english and presentable Skill : - - A strong understanding of corporate law, company regulations, and compliance requirements, - Knowledge in relevant legislation and regulations governing corporate governance, company formations, meetings, and filings. - Must have worked in a listed (BSE) Company - Should have knowledge on SEBI formalities and MCA formalities - Must be able to independently handle compliances related to Board meeting, AGMs etc. - Knowledge of SDS software - Good communication & strong analytical skill Job Description: Overall activities related to Company’s Act & Secretarial matters and various rules and regulation thereunder Conducting Board Meetings, General Meetings, Audit Committee Meeting, etc., as and when needed, , Prepare various draft agenda notes, Notice of Board Meeting, Committee Meeting & Annual General Meeting as per the Companies Act, Take minutes, draft resolutions, and lodge required forms and annual returns with appropriate authorities. File various statutory forms & returns, Maintain and record Statutory Registers as required under the Companies Act & Rules thereunder, Liaising with various statutory bodies like Registrar of Companies, other Government departments, etc. Pay dividends to shareholders and manage share option schemes opted by various shareholders. Formalities of SEBI & BSE / CSE as per Listing Agreement and upload all forms/details/xbrl at BSE & CSE including SDD Compliance Job Type: Full-time Pay: ₹1,000,000.00 - ₹1,200,000.00 per year Ability to commute/relocate: Manicktala, Kolkata, West Bengal: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Notice Period Current Salary Education: Bachelor's (Preferred) Experience: Listed company : 7 years (Preferred) Due diligence : 7 years (Preferred) Company Secretary: 7 years (Preferred) corporate law, company regulations, and compliance: 7 years (Preferred) worked in a listed Company: 7 years (Preferred) Company’s Act & Secretarial matters: 7 years (Preferred) SEBI formalities and MCA formalities: 7 years (Preferred) Language: English (Preferred) License/Certification: Company Secretary (Preferred) Location: Manicktala, Kolkata, West Bengal (Preferred) Work Location: In person

Job ID:42023 Location:LRQA - New Delhi - Kalkaji, Mumbai: Solitaire Corporate Park, Vadodara : Naman House : Haribha Position Category:Business Development Position Type:Employee Regular Who are LRQA? LRQA stands for dedication to clients, market firsts, and deep expertise in risk management. We’ve grown to become a leading global assurance provider, bringing together outstanding expertise in certification, customised assurance, cybersecurity, inspection, and training. While we’re proud of our heritage, it’s who we are today that really matters, because that’s what shapes who we and our clients can become tomorrow. By staying true to our shared values and combining decades of collective experience, we support our clients in building a safer and more sustainable future. What do we do? We help our clients negotiate a rapidly changing world, by working with them to manage and mitigate the risks they face. We specialise in management systems compliance & expert advice across a broad spectrum of standards, schemes & business improvement services to include customised training & assurance. In Inspection Services, we certify safety critical industrial equipment according to recognised codes, standards & regulations. We also partner with companies to provide tailored high-quality inspection services throughout their manufacturing supply chains, making sure equipment is built safely & to their requirements. Our award-winning Cyber Security Business Nettitude, helps clients manage their risks against a backdrop of new threats emerging every day, we focus on the threat in the cyber landscape and provide tailored made solutions so that our clients can manage their risks effectively. Our independence means we provide reliable, impartial, and informed advice. All of this helps us stand by the purpose that drives us every single day, shaping a better future together. LRQA currently operates across 50 countries, has more than 2,500 colleagues, generates £315m in revenue, and supports more than 60,000 clients across a diverse range of sectors and markets. The next chapter for LRQA The future is exciting and rapidly changing. New challenges and opportunities are arising all the time. We’re adapting to these challenges by expanding our portfolio of services and aiming to become the leading digitally enabled assurance provider. With solid expertise and heritage in our sector, coupled with well-timed accelerated investment and a leadership team that is fully committed to delivering our vision, LRQA’s next chapter is set to be an exciting, transformational period of growth. We’re well placed to build on everything we’ve done and further our ambitions for the future. At such an exciting time this is a great opportunity to be part of our next chapter. We are looking for talented people who will support us to build on our strengths and transform our business to be the best partner for our clients. Role Purpose LRQA’s mission is to be the leading digitally enabled assurance provider, helping our clients navigate a changing risk landscape. We will achieve this by being the leading assurance provider in key sectors such as food, cybersecurity and ESG, making it easier for clients to do business with us through our digital transformation, and ultimately delivering a portfolio of services which make the world a cleaner, more sustainable, and safer place. Our Business Assurance Business Unit is a recognised, world-leading professional assurance services organisation. We specialise in management systems compliance & expert advice across a broad spectrum of standards, schemes & business improvement services, including customised training & assurance programs. Reporting into the SAM Sales Manager (HSAM), the purpose of the Strategic Account Manager is to: Develop and win new business opportunities with existing and target strategic accounts Build and maintain strong strategic relationships with key individuals in client accounts Lead the strategic sales priorities and implementation for accounts, based on opportunities, framework and service agreements, to maximise revenue delivery and growth Introduce new products and services which are added to the LRQA portfolio through acquisitions and new product development Support strategic bids and be a major contributor to the bid process and team Be the local lead and representative for colleague’s accounts, where geographical strategic support is needed, including liaison with Strategic Account Managers (GAM’s) to drive sales and pipeline opportunities Responsibilities Results driven delivery You will manage a selection of strategic accounts and be responsible for winning business from a target group of logos, with an annual combined revenue value of £0.5 initially, depending on mixture of existing and new client priorities, working on growing this significantly year on year. You will be responsible for creating the implementation strategy for new sales in your accounts and working with LRQA teams as needed to achieve success. Retention, revenue growth and new logo wins will be the key performance indicators use to measure success. Account Management Skills You will be responsible for the development and delivery of strategic account plans, which maximise the LRQA opportunity for revenue, in line with group growth objectives and priorities. You will ensure continual development of each client’s business focus and strategy, you will grow the network of influencers in each client organisation and will maintain an active pipeline of opportunities, prioritising workload to ensure client satisfaction and maximum revenue growth. This will involve proactive engagement with other LRQA teams, including marketing, Service Delivery (SD) and Service Delivery Support (SDS) as needed to put your account and targets into the best shape possible for success. Pipeline Management Skills You will need to manage your client pipelines to ensure that they are sufficient to meet the relevant targets, engaging with GAM colleagues and other local SAMs to maximise the opportunities you develop, through local relationships and contracts. This will include ensuring the accuracy of values, sales stages, dates of actions and likely closure timelines. Where your overall pipeline is not in the right shape, you will take action to correct this and ensure it gets back on track in a timely manner. Your pipeline will be an accurate reflection of your sales forecast at any given time. Preparation and delivery of account plans You will ensure that any strategic account under the management of your team, has an up to date, viable account plan, which is driving the strategic growth initiatives for the account, and which can be clearly articulated by the relevant salesperson, at any time. You will use account plans to prioritise opportunities, marketing support and team efforts to drive the growth you are tasked with delivering each financial period. Contract renewals and RFP’s You are responsible for managing the retention of all business with your named accounts, minimising the risk of loss to the LRQA business, through timely intervention in any process, preventing the re-tendering of business where possible and re-securing the contract where needed. You will play an active role in new business opportunities, either in a lead or supporting sales position, depending on the winning strategy and relevant skills needed to maximise the opportunity of winning. Problem solving You will be accountable for working with your clients and targets on identifying problems that LRQA can solve via a customised solution of its products and services, underpinned by strong market knowledge and experience. Market knowledge and strategic prioritisation You will maintain a strong strategic knowledge of the market(s) you operate in, ensuring you are able to maintain a strong level of communication with client personnel, using this to open doors for new products and services, and to contribute to strategic discussions around LRQA business plans and growth objectives. Contribution to Sales Meetings and Performance summaries From sales management meetings to BA leadership team meetings, you will be responsible for the production of sales and pipeline reports, performance summaries and updates on specific project actions, ensuring they are accurate and delivered in a timely manner. Key Requirements Demonstrable experience of achieving annual sales targets, selling products and services in a comparable role in a B2B environment, with at least 14-22 years’ experience. Proven experience of working with large strategic organisations to develop sales solutions underpinned by insights, to solve business problems. Previous experience in selling ISO 9001, ISO 14001, ISO 45001, ISO 50001, FSSC 22000, ISO 27001,FSSC 22000,IATF,ISO 1384 Etc. Demonstrable experience of developing contract values with large accounts through year-on-year double digit growth. Ability to communicate fluently in English and a minimum of one other language widely used in businesses in your base region. Experience in preparing and delivering proposal presentations to senior level audience. Experience in managing quotations, bids and proposals, including knowledge of pricing strategies to achieve required margin. Demonstrable experience in working proactively and collaboratively across teams including marketing to achieve growth strategies and targets. Knowledge of standard IT programmes, Salesforce/ Microsoft D365 and comfortable in using proprietory software for business processes. Diversity And Inclusion At LRQA We are on a mission to be the place where we all want to work and we are passionate about embracing different perspectives because we understand the value this brings to our business, our clients and each other. We are all about creating a safer and more sustainable future and our inclusive culture is right at the heart of our business. Together our employees make our communities better and we want you to be part of our diverse team! LRQA is a leading global assurance provider. The integrity and expertise we bring to our partnership with clients support their journey to a safer, more secure and more sustainable future. (Group entities). Copyright © LRQA 2021. All rights reserved. Terms of use. Privacy Policy. Show more Show less

Job Location : Kolkata Position : Company Secretary Experience : min 7 years post company secretary qualification Qualifications : Graduate with Company Secretary Industry : Joining : As soon as possible Skills : Good in english and presentable Skill : - - A strong understanding of corporate law, company regulations, and compliance requirements, - Knowledge in relevant legislation and regulations governing corporate governance, company formations, meetings, and filings. - Must have worked in a listed (BSE) Company - Should have knowledge on SEBI formalities and MCA formalities - Must be able to independently handle compliances related to Board meeting, AGMs etc. - Knowledge of SDS software - Good communication & strong analytical skill Job Description: Overall activities related to Company’s Act & Secretarial matters and various rules and regulation thereunder Conducting Board Meetings, General Meetings, Audit Committee Meeting, etc., as and when needed, , Prepare various draft agenda notes, Notice of Board Meeting, Committee Meeting & Annual General Meeting as per the Companies Act, Take minutes, draft resolutions, and lodge required forms and annual returns with appropriate authorities. File various statutory forms & returns, Maintain and record Statutory Registers as required under the Companies Act & Rules thereunder, Liaising with various statutory bodies like Registrar of Companies, other Government departments, etc. Pay dividends to shareholders and manage share option schemes opted by various shareholders. Formalities of SEBI & BSE / CSE as per Listing Agreement and upload all forms/details/xbrl at BSE & CSE including SDD Compliance Job Type: Full-time Pay: ₹1,000,000.00 - ₹1,200,000.00 per year Ability to commute/relocate: Manicktala, Kolkata, West Bengal: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Notice Period Current Salary Education: Bachelor's (Preferred) Experience: Listed company : 7 years (Preferred) Due diligence : 7 years (Preferred) Company Secretary: 7 years (Preferred) corporate law, company regulations, and compliance: 7 years (Preferred) worked in a listed Company: 7 years (Preferred) Company’s Act & Secretarial matters: 7 years (Preferred) SEBI formalities and MCA formalities: 7 years (Preferred) Language: English (Preferred) License/Certification: Company Secretary (Preferred) Location: Manicktala, Kolkata, West Bengal (Preferred) Work Location: In person

job description for an ** Medical Coders ** ** We Are Hiring Medical Coders (Certified/Non-Certified)** ** Positions Open:** * ED Facility Coder * HCC Coder * Surgery Coder * E/M Coding Specialist * IP DRG * ED Profee * Anesthesia * Radiology ** Contact HR Jenistan : +91 89255 29872** ** Locations:** Chennai | Hyderabad | Pune ** Experience:** 1 to 4 Years ** Certification:** AAPC / AHIMA Certified or Non-Certified with relevant experience ** Joiners:** Immediate Joiners Only ** Salary:** Decent Hike on Current CTC ** Interview Mode:** Virtual --- ### **Job Requirements:** * Strong knowledge of Medical Coding practices and coding guidelines * Hands-on experience in ED, HCC, Surgery, or E/M coding * Good understanding of ICD-10, CPT, and HCPCS * Ability to work independently and deliver quality results **Don't miss this opportunity to grow your career in the medical coding industry!** ---

Use Your Power for Purpose Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring customers and patients receive the medicines they need, precisely when they need them. By collaborating with our forward-thinking engineering team, youll play a key role in accelerating the delivery of medicines to the world. Your innovative ideas and proactive actions will help us imagine new possibilities and bring them to life, making a significant impact on global health. As an Associate in the Global Supply division, you will contribute to improving patients lives while working at Pfizer. Your dedication and expertise will ensure our plants, utility systems, buildings, and equipment are operational, helping us achieve new milestones and assist patients worldwide. What You Will Achieve In this role, you will: Support the operation and troubleshooting of manufacturing equipment and control systems including DeltaV DCS, SCADA & PLCs. Should work in shifts to provide operational support on Automated systems. Support all investigations and audits as needed pertaining to automation subject matter. Responsible for Periodic review of the Automation Systems with support of validation team. Responsible for implementation of compliance initiatives including monitoring of system security procedures and practices and system logins for compliance Generate user requirement specifications for control systems. Author and/or review design documents for projects and process changes Define requirements for vendor design documentation. Review vendor automation design documentation (FS, HDS, SDS, DDS, requirements traceability matrix, code and logic, etc. Execute qualification protocols of automated systems. Prepare risk assessments for automated systems Prepare Change Controls associated with changes to control systems Design and implementation support for functional and process changes, either smaller projects, remediation activities or capital projects Responsible for backup/archiving/restoring of Automation configuration and batch. Understand 21 CFR Part 11, cGAMP, and other regulatory guidance associated with computer / automation-based systems. Develop automation Standard Operating Procedures Here Is What You Need (Minimum Requirements) Bachelors degree with any years of experience, or an Associates degree with 4 years of relevant experience in Instrumentation / Electronics / Computers. Experience in DeltaV DCS, other DCS, SCADA and PLC based systems. Demonstrated ability to write and provide simple and accurate instructions Working experience in pharmaceutical industry Demonstrated computer and technical skills Effective problem-solving capabilities Excellent interpersonal communication and written skills Bonus Points If You Have (Preferred Requirements) Knowledge or experience working in a Good Manufacturing Practices (also cGMP) environment Strong organizational skills Ability to work independently and as part of a team Proactive and self-motivated Work Location Assignment: On Premise Engineering #LI-PFE

We Hiring EM IP/OP Coders/QA Min 3+ Yr of Experience required Certification is Mandatory Education - Only Life Science background Good knowledge in ICD-10, CPT, Modifiers and ETC.., WFO is must. Location: Chennai Contact - 6379093874 Sangeetha

Dear candidates, Greetings from Teleperformance!!! Medical coder with minimum 1 year experience on denial / Surgery coder. certification not Mandatory. Quarterly one month will be night shift - (Both way cab provided) Graduation Mandatory. Looking for immediate joiners. Job Location: AMBIT IT Park - Ambattur. Interested candidate please call Hema HR@8524862257 NOTE: Openings only for Denial and surgery coding Regards Hema Assistant Manager.

2 - 5 year experience required Core specialties: Neuro spine Level 3 surgery, Ortho and EM coding. Certified can only apply Preferred Certifications: CPC, CPC-A, CCS, COC, CIC WFO Contact 8977711182

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Location: Bengaluru, KA, IN Company: ExxonMobil About us At ExxonMobil, our vision is to lead in energy innovations that advance modern living and a net-zero future. As one of the world’s largest publicly traded energy and chemical companies, we are powered by a unique and diverse workforce fueled by the pride in what we do and what we stand for. The success of our Upstream, Product Solutions and Low Carbon Solutions businesses is the result of the talent, curiosity and drive of our people. They bring solutions every day to optimize our strategy in energy, chemicals, lubricants and lower-emissions technologies. We invite you to bring your ideas to ExxonMobil to help create sustainable solutions that improve quality of life and meet society’s evolving needs. Learn more about our What and our Why and how we can work together . ExxonMobil’s affiliates in India ExxonMobil’s affiliates have offices in India in Bengaluru, Mumbai and the National Capital Region. ExxonMobil’s affiliates in India supporting the Product Solutions business engage in the marketing, sales and distribution of performance as well as specialty products across chemicals and lubricants businesses. The India planning teams are also embedded with global business units for business planning and analytics. ExxonMobil’s LNG affiliate in India supporting the upstream business provides consultant services for other ExxonMobil upstream affiliates and conducts LNG market-development activities. The Global Business Center - Technology Center provides a range of technical and business support services for ExxonMobil’s operations around the globe. ExxonMobil strives to make a positive contribution to the communities where we operate, and its affiliates support a range of education, health and community-building programs in India. Read more about our Corporate Responsibility Framework. To know more about ExxonMobil in India, visit ExxonMobil India and the Energy Factor India. What role you will play in our team 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 What you will do Leadership in PS&RA Surveillance Activities Surveillance : Monitor emerging, new, and changing product SHE (Safety, Health, and Environment) regulations through various channels. Evaluation and Interpretation : Assess the impact of these regulations on Product Solutions. Documentation : Maintain up-to-date surveillance logs. Enabling Business Competitiveness and Compliance Regulatory Expertise : Provide technical regulatory expertise and align on interpretation of regulatory requirements. Compliance Support : Ensure compliance with regulations in assigned geographies and interface with other teams for consistent interpretation and timely compliance. Regulatory Compliance Activities Communication : Provide tailored communication to internal and external customers. Safety Data Sheets : Add local regulations to finalize safety data sheets. Product Management : Process product management of change requests and perform product registrations in national registers. Reporting : Conduct sales volume and GHS (Globally Harmonized System) reporting to authority websites. Poison Center Updates : Analyze and process needs for poison center updates. Salesforce Compliance Portal : Manage the portal to ensure prompt feedback on regulatory questions. Safety Data Sheet Distribution : Check distribution reports and initiate corrective actions if needed. Database Management : Manage databases for representative agreements or REACH (Registration, Evaluation, Authorization, and Restriction of Chemicals) registrations. About you Skills and Qualifications Bachelor’s or MSc (Toxicology/Microbiology) with 7 CGPA Minimum 3 years of industry experience Willing to work in shifts (9.00 AM – 6.00 PM IST) Familiarity with regulations for Chemical Classification and Labelling and Product Transportation Classification Your benefits An ExxonMobil career is one designed to last. Our commitment to you runs deep: our employees grow personally and professionally, with benefits built on our core categories of health, security, finance and life. We offer you: Competitive compensation Medical plans, maternity leave and benefits, life, accidental death and dismemberment benefits Retirement benefits Global networking & cross-functional opportunities Annual vacations & holidays Day care assistance program Training and development program Tuition assistance program Workplace flexibility policy Relocation program Transportation facility Please note benefits may change from time to time without notice, subject to applicable laws. The benefits programs are based on the Company’s eligibility guidelines. Stay connected with us Learn more about ExxonMobil in India, visit ExxonMobil India and Energy Factor India. Follow us on LinkedIn and Instagram Like us on Facebook Subscribe our channel at YouTube EEO Statement ExxonMobil is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin or disability status. Business solicitation and recruiting scams ExxonMobil does not use recruiting or placement agencies that charge candidates an advance fee of any kind (e.g., placement fees, immigration processing fees, etc.). Follow the LINK to understand more about recruitment scams in the name of ExxonMobil. Nothing herein is intended to override the corporate separateness of local entities. Working relationships discussed herein do not necessarily represent a reporting connection, but may reflect a functional guidance, stewardship, or service relationship. Exxon Mobil Corporation has numerous affiliates, many with names that include ExxonMobil, Exxon, Esso and Mobil. For convenience and simplicity, those terms and terms like corporation, company, our, we and its are sometimes used as abbreviated references to specific affiliates or affiliate groups. Abbreviated references describing global or regional operational organizations and global or regional business lines are also sometimes used for convenience and simplicity. Similarly, ExxonMobil has business relationships with thousands of customers, suppliers, governments, and others. For convenience and simplicity, words like venture, joint venture, partnership, co-venturer, and partner are used to indicate business relationships involving common activities and interests, and those words may not indicate precise legal relationships. Job Segment: Sustainability, Chemical Research, CSR, Database, Energy, Engineering, Management, Technology

Location: Bengaluru, KA, IN Company: ExxonMobil About us At ExxonMobil, our vision is to lead in energy innovations that advance modern living and a net-zero future. As one of the world’s largest publicly traded energy and chemical companies, we are powered by a unique and diverse workforce fueled by the pride in what we do and what we stand for. The success of our Upstream, Product Solutions and Low Carbon Solutions businesses is the result of the talent, curiosity and drive of our people. They bring solutions every day to optimize our strategy in energy, chemicals, lubricants and lower-emissions technologies. We invite you to bring your ideas to ExxonMobil to help create sustainable solutions that improve quality of life and meet society’s evolving needs. Learn more about our What and our Why and how we can work together . ExxonMobil’s affiliates in India ExxonMobil’s affiliates have offices in India in Bengaluru, Mumbai and the National Capital Region. ExxonMobil’s affiliates in India supporting the Product Solutions business engage in the marketing, sales and distribution of performance as well as specialty products across chemicals and lubricants businesses. The India planning teams are also embedded with global business units for business planning and analytics. ExxonMobil’s LNG affiliate in India supporting the upstream business provides consultant services for other ExxonMobil upstream affiliates and conducts LNG market-development activities. The Global Business Center - Technology Center provides a range of technical and business support services for ExxonMobil’s operations around the globe. ExxonMobil strives to make a positive contribution to the communities where we operate and its affiliates support a range of education, health and community-building programs in India. Read more about our Corporate Responsibility Framework. To know more about ExxonMobil in India, visit ExxonMobil India and the Energy Factor India. What role you will play in our team The Global Hazard Communication Advisor is responsible for delivering Safety Data Sheets (SDS) and related Chemical Management information to support the ExxonMobil Product Safety Policy and regulatory compliance globally The Specialist covers related functions including SDS Authoring, applied toxicology for chemical classification, product stewardship and regulatory interpretation, and related information-management-system support The position works closely with Marketing, Technology, and Regulatory Advisors What you will do Plan and execute SDS and related projects in coordination with business teams and stakeholders Work within established processes to assemble information and publish SDS Assign exposure scenarios and risk management measures for EU-REACH extended SDS development Read and interpret Hazard Communication regulations to determine impacts on product classification and labelling Support business partners in assessing new or reformulated products for classification and labelling purposes Evaluate new chemical classifications and maintain current and accurate data for SDS development Support the Product Stewardship Information Management System functions and interfaces with other systems Utilize software tools to classify product hazards based on composition, physical and chemical properties, and applicable chemical control regulations Support EU REACH product safety dossier development and submission using various tools such as IUCLID Identify and promote continuous improvement opportunities in systems and procedures About You Skills and Qualification BE / B Tech (Chemical / Materials / Polymers / Petroleum) or Masters in Pharmacology, Chemistry, Engineering, or other science discipline with minimum CGPA 6.5 or 65% Minimum 1 years of experience in petrochemical laboratories, or experience in product stewardship, toxicology, or chemical safety function Experience in SDS Authoring is required REACH Regulations is must IT System and Product Stewardship data management experience strongly preferred Preferred Skills and Qualifications Understanding of physical and chemical properties such as density, viscosity, and flash point Familiarity with regulations for Chemical Classification and Labelling and Product Transportation Classification Strong English communication skills Familiarity with common software including MS Excel, Word, PowerPoint Self motivated with ability to work independently and with global teams Well organized with attention to detail and concern for accuracy Your benefits An ExxonMobil career is one designed to last. Our commitment to you runs deep: our employees grow personally and professionally, with benefits built on our core categories of health, security, finance and life. We offer you: Competitive compensation Medical plans, maternity leave and benefits, life, accidental death and dismemberment benefits Retirement benefits Global networking & cross-functional opportunities Annual vacations & holidays Day care assistance program Training and development program Tuition assistance program Workplace flexibility policy Relocation program Transportation facility Please note benefits may change from time to time without notice, subject to applicable laws. The benefits programs are based on the Company’s eligibility guidelines. Stay connected with us Learn more about ExxonMobil in India, visit ExxonMobil India and Energy Factor India. Follow us on LinkedIn and Instagram Like us on Facebook Subscribe our channel at YouTube EEO Statement ExxonMobil is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin or disability status. Business solicitation and recruiting scams ExxonMobil does not use recruiting or placement agencies that charge candidates an advance fee of any kind (e.g., placement fees, immigration processing fees, etc.). Follow the LINK to understand more about recruitment scams in the name of ExxonMobil. Nothing herein is intended to override the corporate separateness of local entities. Working relationships discussed herein do not necessarily represent a reporting connection, but may reflect a functional guidance, stewardship, or service relationship. Exxon Mobil Corporation has numerous affiliates, many with names that include ExxonMobil, Exxon, Esso and Mobil. For convenience and simplicity, those terms and terms like corporation, company, our, we and its are sometimes used as abbreviated references to specific affiliates or affiliate groups. Abbreviated references describing global or regional operational organizations and global or regional business lines are also sometimes used for convenience and simplicity. Similarly, ExxonMobil has business relationships with thousands of customers, suppliers, governments, and others. For convenience and simplicity, words like venture, joint venture, partnership, co-venturer, and partner are used to indicate business relationships involving common activities and interests, and those words may not indicate precise legal relationships. Job Segment: Sustainability, Chemical Research, Embedded, CSR, Risk Management, Energy, Engineering, Technology, Management, Finance

Job Location : Kolkata Position : Company Secretary Experience : min 7 years post company secretary qualification Qualifications : Graduate with Company Secretary Industry : Joining : As soon as possible Skills : Good in english and presentable Skill : - - A strong understanding of corporate law, company regulations, and compliance requirements, - Knowledge in relevant legislation and regulations governing corporate governance, company formations, meetings, and filings. - Must have worked in a listed (BSE) Company - Should have knowledge on SEBI formalities and MCA formalities - Must be able to independently handle compliances related to Board meeting, AGMs etc. - Knowledge of SDS software - Good communication & strong analytical skill Job Description: Overall activities related to Company’s Act & Secretarial matters and various rules and regulation thereunder Conducting Board Meetings, General Meetings, Audit Committee Meeting, etc., as and when needed, , Prepare various draft agenda notes, Notice of Board Meeting, Committee Meeting & Annual General Meeting as per the Companies Act, Take minutes, draft resolutions, and lodge required forms and annual returns with appropriate authorities. File various statutory forms & returns, Maintain and record Statutory Registers as required under the Companies Act & Rules thereunder, Liaising with various statutory bodies like Registrar of Companies, other Government departments, etc. Pay dividends to shareholders and manage share option schemes opted by various shareholders. Formalities of SEBI & BSE / CSE as per Listing Agreement and upload all forms/details/xbrl at BSE & CSE including SDD Compliance Job Type: Full-time Pay: ₹1,000,000.00 - ₹1,200,000.00 per year Ability to commute/relocate: Manicktala, Kolkata, West Bengal: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Notice Period Current Salary Education: Bachelor's (Preferred) Experience: Listed company : 7 years (Preferred) Due diligence : 7 years (Preferred) Company Secretary: 7 years (Preferred) corporate law, company regulations, and compliance: 7 years (Preferred) worked in a listed Company: 7 years (Preferred) Company’s Act & Secretarial matters: 7 years (Preferred) SEBI formalities and MCA formalities: 7 years (Preferred) Language: English (Preferred) License/Certification: Company Secretary (Preferred) Location: Manicktala, Kolkata, West Bengal (Preferred) Work Location: In person

Use Your Power for Purpose At Pfizer, we believe that every role contributes to our mission of improving patients' lives. Whether you are involved in the design and development of manufacturing processes for products or supporting the upkeep of systems, engineering is crucial to ensuring customers and patients receive the medicines they need. By collaborating with our forward-thinking engineering team, you'll play a pivotal role in accelerating the delivery of medicines to the world. Automation Engineer will have responsibility for managing regulatory aspects of the process automation and control systems used in the manufacture of sterile injectable. This position will provide engineering and technical support related to the operation, maintenance, installation, startup/commissioning, testing, and qualification of manufacturing equipment and systems within a sterile injectable manufacturing facility. What You Will Achieve In this role, you will: Support the operation and troubleshooting of manufacturing equipment and control systems including DeltaV DCS, SCADA & PLCs. Support reliability engineering for production and support equipment Provide on the floor operational support as needed Support all investigations and audits as needed pertaining to automation subject matter. Responsible for Periodic review of the Automation Systems with support of validation team. Responsibility for managing regulatory aspects of the site networked engineering data collection, monitoring and SCADA systems Responsible for implementation of compliance initiatives including monitoring of system security procedures and practices and system logins for compliance Generate user requirement specifications for control systems. Author and/or review design documents for projects and process changes Define requirements for vendor design documentation. Review vendor automation design documentation (FS, HDS, SDS, DDS, requirements traceability matrix, code and logic, etc.). Support FAT/commissioning/qualification activities as required Review qualification protocols of automated systems. Support the execution of the qualification of automated control systems. Prepare risk assessments for automated systems Prepare Change Controls associated with changes to control systems Design and implementation support for functional and process changes, either smaller projects, remediation activities or capital projects Support future capital projects and assure site automation standards are followed Assist other departments in evaluating historical process/equipment data Provide automation guidance and training to other functional groups (i.e. Operations, Validation, Maintenance, QA, etc.) Responsible for backup/archiving/restoring of Automation configuration and batch. Understand 21 CFR Part 11, cGAMP, and other regulatory guidance associated with computer / automation-based systems. Develop and implement site automation standards for hardware and software Develop automation Standard Operating Procedures Here Is What You Need (Minimum Requirements) Bachelor of Technology/Engineering in Electronics/Instrumentation Engineering 6 to 8 years’ experience in a combination of process control, automation (PLC, SCADA & DCS) in pharmaceuticals, biotechnology or other life sciences industries. Individual must be capable of reading and understanding electrical control system diagrams (control panel wiring diagrams, loop drawings, panel layout drawings and schedules, etc.). Comfortable walking down control system diagrams and red lining them to reflect as built conditions. Good technical knowledge on field Instrumentation Good technical knowledge of industrial communication networks and related hardware & software. Basic understanding of sequel servers and databases. Familiarity with current industry practices and guidelines including those required / outlined by the FDA, ISO, EU and ICH. Bonus Points If You Have (Preferred Requirements) Relevant pharmaceutical experience Understanding of programming and proficiency in at least one language Knowledge of Good Manufacturing Practices (GMP) Ability to train others effectively Strong problem-solving skills Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Engineering #LI-PFE

Use Your Power for Purpose Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring customers and patients receive the medicines they need, precisely when they need them. By collaborating with our forward-thinking engineering team, you'll play a key role in accelerating the delivery of medicines to the world. Your innovative ideas and proactive actions will help us imagine new possibilities and bring them to life, making a significant impact on global health. As an Associate in the Global Supply division, you will contribute to improving patients' lives while working at Pfizer. Your dedication and expertise will ensure our plants, utility systems, buildings, and equipment are operational, helping us achieve new milestones and assist patients worldwide. What You Will Achieve In this role, you will: Support the operation and troubleshooting of manufacturing equipment and control systems including DeltaV DCS, SCADA & PLCs. Should work in shifts to provide operational support on Automated systems. Support all investigations and audits as needed pertaining to automation subject matter. Responsible for Periodic review of the Automation Systems with support of validation team. Responsible for implementation of compliance initiatives including monitoring of system security procedures and practices and system logins for compliance Generate user requirement specifications for control systems. Author and/or review design documents for projects and process changes Define requirements for vendor design documentation. Review vendor automation design documentation (FS, HDS, SDS, DDS, requirements traceability matrix, code and logic, etc. Execute qualification protocols of automated systems. Prepare risk assessments for automated systems Prepare Change Controls associated with changes to control systems Design and implementation support for functional and process changes, either smaller projects, remediation activities or capital projects Responsible for backup/archiving/restoring of Automation configuration and batch. Understand 21 CFR Part 11, cGAMP, and other regulatory guidance associated with computer / automation-based systems. Develop automation Standard Operating Procedures Here Is What You Need (Minimum Requirements) Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience in Instrumentation/Electronics/Computers. Experience in DeltaV DCS, other DCS, SCADA and PLC based systems. Demonstrated ability to write and provide simple and accurate instructions Working experience in pharmaceutical industry Demonstrated computer and technical skills Effective problem-solving capabilities Excellent interpersonal communication and written skills Bonus Points If You Have (Preferred Requirements) Knowledge or experience working in a Good Manufacturing Practices (also cGMP) environment Strong organizational skills Ability to work independently and as part of a team Proactive and self-motivated Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Engineering #LI-PFE

Job Title : Senior Data Scientist (SDS 2) Experience: 4+ years Location : Bengaluru (Hybrid) Company Overview: Akaike Technologies is a dynamic and innovative AI-driven company dedicated to building impactful solutions across various domains . Our mission is to empower businesses by harnessing the power of data and AI to drive growth, efficiency, and value. We foster a culture of collaboration , creativity, and continuous learning , where every team member is encouraged to take initiative and contribute to groundbreaking projects. We value diversity, integrity, and a strong commitment to excellence in all our endeavors. Job Description: We are seeking an experienced and highly skilled Senior Data Scientist to join our team in Bengaluru. This role focuses on driving innovative solutions using cutting-edge Classical Machine Learning, Deep Learning, and Generative AI . The ideal candidate will possess a blend of deep technical expertise , strong business acumen, effective communication skills , and a sense of ownership . During the interview, we look for a proven track record in designing, developing, and deploying scalable ML/DL solutions in a fast-paced, collaborative environment. Key Responsibilities: ML/DL Solution Development & Deployment: Design, implement, and deploy end-to-end ML/DL, GenAI solutions, writing modular, scalable, and production-ready code. Develop and implement scalable deployment pipelines using Docker and AWS services (ECR, Lambda, Step Functions). Design and implement custom models and loss functions to address data nuances and specific labeling challenges. Ability to model in different marketing scenarios of a product life cycle ( Targeting, Segmenting, Messaging, Content Recommendation, Budget optimisation, Customer scoring, risk and churn ), and data limitations(Sparse or incomplete labels, Single class learning) Large-Scale Data Handling & Processing: Efficiently handle and model billions of data points using multi-cluster data processing frameworks (e.g., Spark SQL, PySpark ). Generative AI & Large Language Models (LLMs): Leverage in-depth understanding of transformer architectures and the principles of Large and Small Language Models . Practical experience in building LLM-ready Data Management layers for large-scale structured and unstructured data . Apply foundational understanding of LLM Agents, multi-agent systems (e.g., Agent-Critique, ReACT, Agent Collaboration), advanced prompting techniques, LLM eval uation methodologies, confidence grading, and Human-in-the-Loop systems. Experimentation, Analysis & System Design: Design and conduct experiments to test hypotheses and perform Exploratory Data Analysis (EDA) aligned with business requirements. Apply system design concepts and engineering principles to create low-latency solutions capable of serving simultaneous users in real-time. Collaboration, Communication & Mentorship: Create clear solution outlines and e ffectively communicate complex technical concepts to stakeholders and team members. Mentor junior team members, providing guidance and bridging the gap between business problems and data science solutions. Work closely with cross-functional teams and clients to deliver impactful solutions. Prototyping & Impact Measurement: Comfortable with rapid prototyping and meeting high productivity expectations in a fast-paced development environment. Set up measurement pipelines to study the impact of solutions in different market scenarios. Must-Have Skills: Core Machine Learning & Deep Learning: In-depth knowledge of Artificial Neural Networks (ANN), 1D, 2D, and 3D Convolutional Neural Networks (ConvNets), LSTMs , and Transformer models. Expertise in modeling techniques such as promo mix modeling (MMM) , PU Learning , Customer Lifetime Value (CLV) , multi-dimensional time series modeling, and demand forecasting in supply chain and simulation. Strong proficiency in PU learning, single-class learning, representation learning, alongside traditional machine learning approaches. Advanced understanding and application of model explainability techniques. Data Analysis & Processing: Proficiency in Python and its data science ecosystem, including libraries like NumPy, Pandas, Dask, and PySpark for large-scale data processing and analysis. Ability to perform effective feature engineering by understanding business objectives. ML/DL Frameworks & Tools: Hands-on experience with ML/DL libraries such as Scikit-learn, TensorFlow/Keras, and PyTorch for developing and deploying models. Natural Language Processing (NLP): Expertise in traditional and advanced NLP techniques, including Transformers (BERT, T5, GPT), Word2Vec, Named Entity Recognition (NER), topic modeling, and contrastive learning. Cloud & MLOps: Experience with the AWS ML stack or equivalent cloud platforms. Proficiency in developing scalable deployment pipelines using Docker and AWS services (ECR, Lambda, Step Functions). Problem Solving & Research: Strong logical and reasoning skills. Good understanding of the Python Ecosystem and experience implementing research papers. Collaboration & Prototyping: Ability to thrive in a fast-paced development and rapid prototyping environment. Relevant to Have: Expertise in Claims data and a background in the pharmaceutical industry . Awareness of best software design practices . Understanding of backend frameworks like Flask. Knowledge of Recommender Systems, Representative learning, PU learning. Benefits and Perks: Competitive ESOP grants. Opportunity to work with Fortune 500 companies and world-class teams. Support for publishing papers and attending academic/industry conferences. Access to networking events, conferences, and seminars. Visibility across all functions at Akaike, including sales, pre-sales, lead generation, marketing, and hiring. Appendix Technical Skills (Must Haves) Having deep understanding of the following Data Processing : Wrangling : Some understanding of querying database (MySQL, PostgresDB etc), very fluent in the usage of the following libraries Pandas, Numpy, Statsmodels etc. Visualization : Exposure towards Matplotlib, Plotly, Altair etc. Machine Learning Exposure : Machine Learning Fundamentals, For ex: PCA, Correlations, Statistical Tests etc. Time Series Models, For ex: ARIMA, Prophet etc. Tree Based Models, For ex: Random Forest, XGBoost etc.. Deep Learning Models, For ex: Understanding and Experience of ConvNets, ResNets, UNets etc. GenAI Based Models : Experience utilizing large-scale language models such as GPT-4 or other open-source alternatives (such as Mistral, Llama, Claude) through prompt engineering and custom finetuning. Code Versioning Systems : Github, Git If you're interested in the job opening, please apply through the Keka link provided here: https://akaike.keka.com/careers/jobdetails/26215 Show more Show less

Overview Job Title: RA Assistant Location: Chennai Objective The Regulatory Affairs (RA) Assistant is responsible for supporting the regulatory compliance efforts within the region. This involves ensuring adherence to local and international regulatory standards, assisting with product registrations, maintaining documentation, and liaising with regulatory agencies. The RA Assistant plays a key role in helping the business meet compliance requirements and facilitates a smooth regulatory process. The role also provides administrative and operational support to the Regulatory Affairs team for smooth functioning Responsibilities Regulatory Compliance and Documentation Management: Maintain accurate knowledge of local regulatory requirements and ensure product compliance with national and/or international regulations. Develop and finalize product labels in alignment with country-specific requirements and oversee approval and production processes for India manufacturing. Create and maintain primary standard documents (including product specification, SDS, label, etc.) Support on BOM, variant and sample code creation. Regulatory Registrations, Stakeholder Liaison and Communication: Assist in preparing documents for product registrations dossier, imports and exports and custom clearance. Support the preparation of bi-annual reports such as heavy metal analyses for submission to FSSAI. Assist Manage FSSAI Manufacturing, Import, and Export Licenses for KFT products. Act as a liaison with regulatory officials, internally and externally, to ensure smooth information exchange in India. Support customer questionnaires, vendor registrations, and other regulatory or compliance tasks as needed. Audit and Training Support: Participate/support in internal audits and certifications renewal (E.g.: FOSTAC, HALAL, FSSC22000, etc.) Project Involvement: Support on PTP, PRI, PIP, or any other initiatives under the guidance of the Manager. Conduct research to support regulatory strategies and processes. Qualifications Bachelor's or Master’s degree in Food Science, Chemistry, or a related field with 1-2 years of expereince . Preferably with knowledge of regulatory aspects in the food industry. Show more Show less

Job Location : Kolkata Position : Company Secretary Experience : min 7 years post company secretary qualification Qualifications : Graduate with Company Secretary Industry : Joining : As soon as possible Skills : Good in english and presentable Skill : - - A strong understanding of corporate law, company regulations, and compliance requirements, - Knowledge in relevant legislation and regulations governing corporate governance, company formations, meetings, and filings. - Must have worked in a listed (BSE) Company - Should have knowledge on SEBI formalities and MCA formalities - Must be able to independently handle compliances related to Board meeting, AGMs etc. - Knowledge of SDS software - Good communication & strong analytical skill Job Description: Overall activities related to Company’s Act & Secretarial matters and various rules and regulation thereunder Conducting Board Meetings, General Meetings, Audit Committee Meeting, etc., as and when needed, , Prepare various draft agenda notes, Notice of Board Meeting, Committee Meeting & Annual General Meeting as per the Companies Act, Take minutes, draft resolutions, and lodge required forms and annual returns with appropriate authorities. File various statutory forms & returns, Maintain and record Statutory Registers as required under the Companies Act & Rules thereunder, Liaising with various statutory bodies like Registrar of Companies, other Government departments, etc. Pay dividends to shareholders and manage share option schemes opted by various shareholders. Formalities of SEBI & BSE / CSE as per Listing Agreement and upload all forms/details/xbrl at BSE & CSE including SDD Compliance Job Type: Full-time Pay: ₹1,000,000.00 - ₹1,200,000.00 per year Ability to commute/relocate: Manicktala, Kolkata, West Bengal: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Notice Period Current Salary Education: Bachelor's (Preferred) Experience: Listed company : 7 years (Preferred) Due diligence : 7 years (Preferred) Company Secretary: 7 years (Preferred) corporate law, company regulations, and compliance: 7 years (Preferred) worked in a listed Company: 7 years (Preferred) Company’s Act & Secretarial matters: 7 years (Preferred) SEBI formalities and MCA formalities: 7 years (Preferred) Language: English (Preferred) License/Certification: Company Secretary (Preferred) Location: Manicktala, Kolkata, West Bengal (Preferred) Work Location: In person