About The Role :: Job Title:KYC Associate Location:Jaipur, India Role Description The Know Your Client (KYC) Analyst focuses on client onboarding (COB) and exceptions in line with regulatory standards and jurisdictions. The KYC Analyst provides regular communication to senior bank stakeholders on changes in KYC, Anti Money Laundering (AML) and Anti Financial Crime (AFC) areas and ensures any changes required are implemented with minimum disruptions. The KYC Analyst also assists the banks clients, managing all KYC and account opening requirements with appropriate governance and controls. They operate in an environment of strict adherence to Standard Operating procedures (SOPs) and Operation Level Agreements (OLAs) to achieve accurate and timely account opening to help execute trades What we'll offer you As part of our flexible scheme, here are just some of the benefits that youll enjoy, Best in class leave policy. Gender neutral parental leaves 100% reimbursement under childcare assistance benefit (gender neutral) Sponsorship for Industry relevant certifications and education Employee Assistance Program for you and your family members Comprehensive Hospitalization Insurance for you and your dependents Accident and Term life Insurance Complementary Health screening for 35 yrs. and above Your key responsibilities The Know Your Client (KYC) Analyst focuses on client onboarding (COB) and exceptions in line with regulatory standards and jurisdictions. The KYC Analyst provides regular communication to senior bank stakeholders on changes in KYC, Anti Money Laundering (AML) and Anti Financial Crime (AFC) areas and ensures any changes required are implemented with minimum disruptions. The KYC Analyst also assists the banks clients, managing all KYC and account opening requirements with appropriate governance and controls. They operate in an environment of strict adherence to Standard Operating procedures (SOPs) and Operation Level Agreements (OLAs) to achieve accurate and timely account opening to help execute trades Your skills and experience Should have more than 5 years experience in Corporates and with good communication and system knowledge. How we'll support you Training and development to help you excel in your career. Coaching and support from experts in your team. A culture of continuous learning to aid progression. A range of flexible benefits that you can tailor to suit your needs. About us and our teams Please visit our company website for further information: https://www.db.com/company/company.htm We strive for a culture in which we are empowered to excel together every day. This includes acting responsibly, thinking commercially, taking initiative and working collaboratively. Together we share and celebrate the successes of our people. Together we are Deutsche Bank Group. We welcome applications from all people and promote a positive, fair and inclusive work environment.

About The Role :: Job Title :KYC- Analyst, NCT Location :Mumbai, India Role Description: Provide leadership, analysis and compliance policy guidance/support to facilitate and improve productivity of team. Act as a subject matter expert (SME) on client due diligence, fronting the KYC team and liaising with all levels of management across customers, Global Banking & Markets ,GTB business lines, Compliance, and other support areas to ensure and efficient, flexible and accurate process for on boarding and revalidating clients. What we'll offer you As part of our flexible scheme, here are just some of the benefits that youll enjoy Best in class leave policy Gender neutral parental leaves 100% reimbursement under childcare assistance benefit (gender neutral) Sponsorship for Industry relevant certifications and education Employee Assistance Program for you and your family members Comprehensive Hospitalization Insurance for you and your dependents Accident and Term life Insurance Complementary Health screening for 35 yrs. and above Your key responsibilities Demonstrate complete end to end understanding of the process along with the associated risks Ensure all the assigned cases are proactively managed with valid observations and without any escalations from the case managers / Business Ensure all the queries from the group inbox are responded in a timely manner without any follow up from managers, case managers or Business Timely escalations of Issues and Risks identified to management. Adherence to Quality Checklist recommended & ensure required details are captured & complete in all respects. Minimise client outreach and enable request for all required documentation the first time round Ensure no KYC is complete without a TAX Form Ensure the QA Scores are 100% and AFC scores at 100 % Ensure all the adoptions are completed with the first time pass rate of 100% accuracy in line with project Mercury. Actively supports the various Audit / Compliance requests without any follow ups from the managers Drives the Daily knowledge share sessions and actively takes part in order to increase the teams understanding of the process Ensure Quality of service and file production across all data points on a client file is accurate Your skills and experience Graduates with good academic records Overall experience of atleast 1 years in the Banking/Finance industry KYC background with a minimum of 1 years experience working in Client Onboarding team. Good knowledge of regulatory trends and developments Proven ability to prioritize competing demands . Effective communication skills to be able to manage relationships with clients virtually. Able to cope well under pressure and meet deadlines Eye for detail and willingness to question current state practices Independent, self-motivated and a team player. Ability to use sound judgment to determine due diligence quality and if meets regulatory standards. Ability to apply regulatory guidance to review process in absence of written policy Excellent verbal and written communication skills How we'll support you Training and development to help you excel in your career Coaching and support from experts in your team A culture of continuous learning to aid progression A range of flexible benefits that you can tailor to suit your needs

DRA Manager Experience- 15+ years Salary Package- 13-17 LPA Must have experience in regulatory Countries dossier preparation and working Should have worked in Injectable Unit location- Baddi Himachal Pradesh

•6 + years' professional experience in medical device regulatory , Experience with systems for quality management, product development, and follow-up of procedures. • E xperience in medical device regulatory Quality systems EU MDR, US FDA 510(k) and closely working R&D, Regulatory Affairs organizations • Expertise in interpreting & implementing various medical device standards and guidance's, such as IEC 60601-1, ISO 10993-1:2018; ISO15223-2021; ISO 14971:2019; EN ISO 13485; ISO 11607-1,2; and EN ISO 11137-1 and MEDDEV 2.7/4 • Knowledge and application of medical device QMS is required (e.g., ISO 13485, MDSAP, EU MDR, Risk Management etc.) • Ensures that appropriate Quality Plans are made that include all stages product life cycle ,supports Quality Plan • Validate key design inputs like : Usability, Reliability, Performance, Supportability, Manufacturability, Safety, Security, Privacy, Serviceability, Sustainability etc. • Provides effective oversight of the execution of the Quality Plan, Risk Management activities, and all design related activities during the product/system life cycle • Performs independent technical assessment on product quality performance and post-market product quality analysis • Can Lead quality related problem solving and root cause analysis during design and manufacturing • Uses post-market analytics and statistics to report on product quality performance in the field (provide feedback to manufacturing, suppliers or design teams) and initiates field actions when required • Compliance focused • Be able to handle ad-hoc changes in priority/planning and independently. • Be able to think from customer expectation perspective • Be able to work in different teams simultaneously • Communicative & disciplined team worker.

Looking out 3 HEADS (at Senior Manager/ DGM level) for 3 STATES Gujarat / Rajasthan / Maharashtra and MP ) for handling state level Compliance and Regulatory for WIND/SOLAR projects permissions and approvals Experience: 13+ years in state compliance and regulatory management within the renewable energy sector Reporting To: Projects Head Key Responsibilities: Approvals and Clearances: Manage and secure all necessary approvals from state and central authorities, including: DISCOMs, Transcos, CEIG, PTCC, Section 68, SLDC NOC, and synchronization approvals. • Transmission line schedules, tower/pole schedules, and other regulatory requirements for successful project commissioning. Regulatory Compliance: Conduct connectivity and feasibility studies for evacuation capacity in new projects. Ensure compliance with state and central regulations throughout the project lifecycle. Stakeholder Management: Liaise with government agencies, DISCOMs, and other regulatory bodies to expedite approvals. Address critical issues, identifying solutions to maintain project timelines. Project Milestone Management: Drive regulatory and compliance activities in line with project schedules and milestones. Mitigate risks and resolve bottlenecks affecting project execution and commissioning. Documentation and Reporting: Maintain accurate and comprehensive records of all regulatory and compliance documentation. Prepare and submit regular updates on the status of approvals and compliance activities to the Projects Head. Qualifications and Skills Education: any graduate Experience: 13+ years in regulatory compliance roles, preferably in large-scale renewable energy projects. Skills: Strong knowledge of regulatory frameworks and government approval processes in the energy sector. • Proven ability to liaise effectively with state and central authorities. • Exceptional problem-solving, communication, and negotiation skills. • Proficiency in managing multiple stakeholders and driving timely project approvals.

DominicLewis has been mandated to hire for SCM Risk management role Identify and Manage Supplier Information: Lead the deployment and integration of supply chain risk monitoring platforms (Resilinc, Riskmethods, Ever stream) to track and manage supply chain disruptions. Provide training and ongoing support to team members on the use of these tools. Monitor supply chain risk indicators such as geopolitical issues, financial risk, natural disasters, supplier disruptions, and regulatory changes using risk monitoring software. Maintain a risk register, documenting critical suppliers, materials, and transportation routes, and ensuring contingency plans are in place. Make sure we have supplier responses from both timeliness and completeness perspectives whenever there is an event at the supplier location. Ensure the correct address details are mapped in the risk monitoring tool, focusing on the actual manufacturing locations of suppliers, rather than their office or corporate headquarters. Accurately map and manage the right contact information for suppliers within the risk management platform to ensure timely communication and support. Regularly (Once in six month) survey Tier 1 suppliers to keep data current. Prioritize critical suppliers which will be a part of a Supplier Relationship Management (SRM) program. Identify the accountable for initial review of the event and activate emergency response team. Based on the severity of an event, establish response triggers and thresholds. For example, activate emergency response teams and activate your BCP's. Clearly define who is a part of emergency response team. For example, representations from manufacturing, procurement, quality, logistics, communications and product teams. Work with procurement teams to assess supplier risk profiles and ensure all critical suppliers are monitored through risk management tools. Generate and distribute regular reports on supply chain risks to key stakeholders, including leadership and operational teams. Communicate risk findings and recommend actions to mitigate potential impacts on supply chain operations. Regularly review and optimize the effectiveness of risk monitoring tools and processes. Keep up to date with the latest developments in supply chain risk management, including new technologies and methodologies. Suggest improvements to current risk management frameworks, ensuring alignment with business objectives and best practices. Supply Chain Optionality Assessment: Define and identify the in-scope data parts necessary for the optionality assessment. Collaborate with the respective assessors to ensure a thorough and accurate evaluation. Review the quality of the assessments to maintain high standards and relevance. Monitor and communicate all KPIs related to the optionality assessment to ensure transparency and alignment with business objectives. Team Management: Oversee and coordinate the activities of team members to ensure alignment with organizational goals and project deadlines. Provide guidance, support, and development opportunities to team members to enhance their performance and career growth. Foster a collaborative and productive team environment by facilitating effective communication and resolving any conflicts that arise.

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Job Purpose: Responsible for management of scheduled and unscheduled aggregate reports including but not limited to Periodic Safety Reports (PSRs) including Periodic Safety Update Reports (PSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), Addendum to Clinical Overviews (ACOs), Semi-Annual Safety Reports (SASRs), Corporate Addendum Reports, United States Periodic Adverse Drug Experience Reports (PADERs), Development Safety Update Reports (DSURs), Annual Risk-Benefit Evaluation (ARBE) report, Risk Management Plan (RMP), Safety statements, Health Hazard Evaluation (HHE), Drug Safety Report (DSR), Clinical Overview (CO), Safety Evaluation Report (SER), Investigational New Drug Annual Report (INDARs) as well as preparing document of comparison between local and global labeling document (if applicable) and checking of International Non-proprietary names (INNs) for inclusion in a PSR as per client requirements and signal detection and management (where applicable). Generating Line Listings, creating drug lists/drug folders, performing regulatory submissions, tests electronic submissions gateways, and tracking compliance monitoring of submissions in accordance with client/international conventions Responsible for preparing the narratives associated with the client’s/sponsor’s products from clinical trials for Clinical Study Reports (CSRs) or in order to support any health authority requests in accordance with regulatory and client’s/sponsor’s requirements. Scheduling and coordinating meetings/ Drafting meeting agenda and minutes/Tracking action items and soliciting follow-up for open issues Key Accountabilities : Note: The below statements describe the general nature and level of the work being performed and are not an exhaustive list of all responsibilities required for the position. Responsibilities vary as applicable Accountability & Supporting Activities Aggregate reports Preparing/updating/merging RMPs/Company Core-RMPs (CC-RMPs), preparing a health authority response document along with RMS update in accordance with client requirements/conventions and SOPs. Managing scheduled and unscheduled aggregate reports including but not limited Periodic Safety Update Reports (PSURs), Periodic Benefit Risk Evaluation Reports (PBRERs), Addendum to Clinical Overviews (ACOs), Semi-Annual Safety Reports (SASRs), Corporate Addendum Reports, United States Periodic Adverse Drug Experience Reports (PADERs), Development Safety Update Reports (DSURs), Annual Risk- Benefit Evaluation (ARBE) report Safety statements, Health Hazard Evaluation (HHE), Drug Safety Report (DSR), Clinical Overview (CO), Safety Evaluation Report (SER), Investigational New Drug Annual Report (INDARs), comparison document between local and global labeling document (if applicable)and checking of International Non-proprietary names (INNs) for inclusion in a PSR as per client requirements and conventions and SOPs Conducting critical appraisal and systematic review of literature with a focus on background epidemiology, specifically information on the incidence, prevalence and risk factor in patient populations, for inclusion in drug Safety Reports and RMPs Providing input and developing literature search strategies for the epidemiology section of safety reports Applying epidemiological methods and calculations to data available inliterature to support the background rates of the issues under evaluation for the safety reports Generating Line Listings for submissions/ to identifying discrepancies and ensuring resolution of the discrepancies Revising document drafts based on the review comments from team members to ensure inclusion of all relevant input. Ensuring that all work is complete and of high quality prior to team or client distribution. Confirm data consistency and integrity across the document. Performing aggregate report compliance activities including quality review to check the data/facts and internal consistency across various type of aggregate reports including but not limited to PBRERs, Ad hocs, HHEs, LJDs, tables, RMP, Pharmacovigilance System Master File (PSMF) document (as applicable) Distributing of final reports to the stakeholders including partners, affiliates and submission to health authorities, according to the agreed timelines, distribution lists and email templates (as required) Scheduling and coordinating meetings/ Drafting meeting agenda and minutes/Tracking action items and soliciting follow-up for open issues Clinical Study Report Narratives Coordinates and liaises with the members of Study Management Team (SMT)/Study In-charge or equivalent, to discuss the narrative template development process, narrative categories and review of the narratives (as required) Serves as primary client contact for narrative writing for an assigned study, agreeing/negotiating deliverable timelines, and addressing/resolving any narratives related issues (as required) Prepares clear and accurate narratives based on Clinical Database and Safety Database outputs provided by the client and ensures their appropriate medical cohesiveness and assessment in accordance with the client’s and Parexel’s conventions/guidelines and Standard Operating Procedures Performs quality checks on the drafted narratives as required Ensures the work is complete and of high quality, including final quality control checks, compilation and formatting. Provides CSR narrative review support to the SMT where requested Signal Detection and Management Perform signal detection review and analysis (qualitative and quantitative) from various sources e.g. regulatory authority database, client database, literatures, regulatory authority websites etc. Responsible for the end-to-end signal management process (i.e. signal tracking, signal assessment/data analysis, leading review meetings, presenting, etc.) in collaboration with the GSO Conduct/support signal detection and evaluation activities according to SOPs and guidelines General Maintaining a good working knowledge of the adverse event safety profile of the assigned drugs, labeling documents, client’s guidelines, procedures and SOPs, and international drug safety regulations Maintaining an awareness of global regulatory reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for the adverse event reporting Maintaining a good working knowledge of the assigned Clinical studies for narratives Ensuring that all work is complete and of high-quality Attending/conducting internal, drug safety and project specific training sessions Preparation for, participation in, and follow up on audits and inspections Maintaining an awareness of the performance metrices measured by the client and striving to remain within established limits Delegating work as appropriate to Associate Medical Writer and Medical Writer I Striving to enhance client’s satisfaction based on feedback provided by the client Imparting project specific trainings to the new starts as required. Serving as the primary client contact, liaising and collaborating with the relevant function at the client’s end to facilitate the delivery of high-quality work Evaluating and incorporating reviewer comments in draft reports and liaising with relevant contributors for resolution of comments Mentoring new recruits in the team, if required Archiving the source documents and relevant emails as required Responding to clients/customers in a timely manner Participating in departmental or interdepartmental process improvement and training initiatives (if required) Skills : Analytical and problem-solving skills Excellent interpersonal skills Excellent verbal / written communication skills Excellent organizational and prioritization skills Ability to work collaboratively and effectively in a team environment Client focused approach to work Ability to evaluate data and draw conclusions independently A flexible attitude with respect to work assignments and new learning Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail Ability to understand all necessary steps in a project, plan steps ahead, and identify critical paths. Fluency in written and spoken English Computer proficiency, IT skills, the expertise and an ability to work with web-based applications, and familiarity with the Windows Operating system and the MS Office suite (Word/Excel/Power Point) Capability to make concise, accurate and relevant synopses of medical text and data, and the ability to write unambiguous medical text Typing and transcription accuracy Awareness of global culture and willingness to work in a matrix environment Knowledge and Experience : Relevant experience is desirable in Regulatory/ Pharmacovigilance or related field. Good knowledge of medical terminologies Education : Science/Medicine degree: The minimum qualification required would be a university degree in life Sciences/ Health or Biomedical Sciences (Pharmacy, microbiology, Biochemistry, Biotechnology, Biophysics etc.) A degree in Medicine/Dentistry/Physiotherapy/Experimental Medicine/Nursing, which involves patient exposure in hospital-based environment, would be an advantage

About The Role : Experience in Risk, Compliance, Assurance and Regulatory areas. Preferred candidate with professional consulting experience in risk management ideally with a Big4 or similar large consulting firm. Good understanding of Technology Risk and Compliance frameworks is preferred. Ensure strategic objectives are implemented, risks managed, and benefits realised. Advise the projects and programs on how to identify, monitor, measure and manage existing and emerging risks. Provide independent oversight and challenge the effectiveness of risks and controls during pre and post implementation of projects. Good communication and presentation skills with a proven track record in stakeholder engagement and influencing skills. Ability to plan and prioritise to manage multiple work streams/tasks simultaneously. Candidates with certifications like CISA, CRISC, and PRINCE2/Agile will be preferred. Primary Skills Risks and Controls Management within technology space Technology Insight (Infrastructure, Data, Cloud and Service Management) Project Lifecycle Management Stakeholder engagement Secondary Skills Team Management Presentation skills Inclusive Communication Multi-Tasking

Skill required: IX Intelligent Capital Project Operations - Low Carbon Grid Capital Projects Designation: Capital Projects Management Assoc Mgr Qualifications: BE/BTech Years of Experience: 10 to 14 years What would you do? We are seeking a highly skilled and experienced Senior Power System Engineer to join our engineering team. The ideal candidate will have extensive experience in power systems design, analysis, and operation, along with the ability to lead projects and mentor junior engineers. You will be responsible for providing technical expertise in the planning, design, operation, and maintenance of electrical power systems, both for renewable and conventional energy sources. What are we looking for? Education:Bachelor's degree in Electrical Engineering (or related field) is required.A Master's degree or higher is preferred.Experience:experienced in power system engineering, with a strong background in system design, analysis, and protection.Experience in managing and leading teams of engineers on large projects.Proven experience with power system modeling software such as ETAP, PSS/E, DigSILENT PowerFactory, CYME or similar.Skills:Strong understanding of power system components, including transformers, circuit breakers, relays, and control systems.In-depth knowledge of power system analysis, protection, and control.Experience in renewable energy integration and grid modernization projects.Proficiency in electrical CAD software, simulation tools, and system modeling.Excellent problem-solving and analytical skills.Strong communication skills and ability to work with a diverse team.Experience in high-voltage and substation design.Familiarity with industry codes and standards (IEEE, IEC, ANSI, etc.).Knowledge of energy management systems and SCADA systems. Roles and Responsibilities: Design & Analysis:Lead the design and analysis of electrical power systems including substations, transmission lines, distribution systems, and energy management systems.Perform system modeling, load flow, short circuit, protection coordination, and stability studies to ensure system stability and reliability.Review and provide technical input into the development of power system projects, ensuring compliance with relevant standards and regulations.Project Management:Manage and oversee power system projects from conceptual design through to construction and commissioning.Collaborate with multidisciplinary teams, including electrical, mechanical, and civil engineers, to deliver projects on time and within budget.Prepare technical reports, specifications, and documentation for projects.Technical Leadership & Mentorship:Provide technical leadership and mentorship to junior engineers and project teams.Review work and provide guidance on complex engineering problems and solutions.Keep up-to-date with emerging technologies in the power systems industry.Power System Protection & Control:Design, test, and implement protection and control schemes for electrical systems.Ensure the integration of protective devices and relays, as well as coordination with existing systems.Perform fault analysis and develop system protection strategies to minimize system risks.Compliance & Standards:Ensure all designs, operations, and installations comply with international standards, safety regulations, and best practices.Participate in technical audits, risk assessments, and compliance reviews.Prepare reports for regulatory bodies and clients as required.Troubleshooting & Maintenance:Troubleshoot and resolve complex power system issues, including fault detection and correction.Provide technical support for the operation, maintenance, and optimization of existing systems.Continuous Improvement:Drive the continuous improvement of power system designs, operations, and practices.Propose innovative solutions to enhance system performance and efficiency. Qualifications BE,BTech

Job Description Develops and executes strategies for connection and purchase of energy and utilities services, as well as identify business opportunity to cut down cost and mitigate risks through innovation and collaboration. Maintains an advanced knowledge of the energy industry and regulatory practices to obtain reliable supply solutions and develop competitive pricing structure and rate mechanism. Leverages and applies strong understanding of contracting and negotiating, tariff design, risk mitigation, renewables, regulatory policy and market rules and supplier relationship management particularly with monopoly utilities, regulatory agencies including energy services and solutions provider to manage relationships and provide predictable cost, quality, availability, and sustainable supply chain technology solutions with adherence to procurement policies. Owns relationships and coordinates purchasing activities with cross functional teams to secure capacities in a cost effective and timely manner. Ensures that supply strategies meets the business demand, quality and cost expectations. Works closely with internal and external stakeholders to advocate rate design structure, supply configuration designs to meet desired capability for serving the demand and fulfil the business objective. Works with internal teams for creation of supply chain solutions to influence cost and provide insight on future trends and potential risk impacts. Conducts periodic executive reviews of energy sourcing strategy in partnership with internal teams and suppliers to shape strategic business objectives and influence investment decision through aligned roadmaps. Leads energy sustainability and build strategies to assess market opportunities that will help corporate to achieve renewable energy goal across global operations. Work with consultants and market research agencies to mitigate pricing risks for qualification and selection of renewable PPAs. Collaborate with cross functional team to drive capacity needs, understand energy market, regulatory process and define cost reduction roadmaps and decarbonization solutions through detailed understanding of financial targets, business objectives, and margins. Qualifications Minimum qualifications are required to be initially considered for this position. Preferred qualifications are in addition to the minimum requirements and are considered a plus factor in identifying top candidates.Minimum Qualifications: Bachelor or post graduate degree in the Engineering, Science or Supply Chain Management or professional experience in energy or utility industry. Minimum 5 years of relevant procurement experience in energy related business and utility industry experience in the Asia regions covering Malaysia, China and Vietnam is essential. Experience in category strategy management and managing complex contract and execution strategies to achieve cost advantage. Indepth, understanding of the regulatory policy and market rules across the region for the generation and supply of energy and water services. Collaborate with internal team for site selection support and gap assessment activities for infrastructure capacity development. Ability to adapt to market dynamics and drive complex energy transactions. A self-starter with strong leadership skills, making decision that shape the path to success. Preferred Qualifications: Experience interacting with relevant state/federal government agencies, officials and representatives from utilities in Asian countries to build unique strategies for delivering results. Understanding of technology evolution, market trends and data analytics is desired. Experience in delivering advanced sustainability program and framework through efficient and low emission technology solutions. Requirements listed would be obtained through a combination of industry relevant job experience, internship experiences and or schoolwork/classes/research.

Role & responsibilities In Power Management S/he shall have the expertise in coordinating with all statutory entities like TANGEDCO/ TANTRANSCO/TNERC/ CEIG for supporting internal cross functional team for Shall have the experience in effective coordination with various departments of utilities for the processing of initial applications for power sanction and for further processes up to the stage of commissioning of both side infrastructure at utility and consumer end (AIS or GIS) substations respectively. Shall have understanding and knowledge on power infrastructures like bay extension works at utility substations (22/33/110/230 KV) and related equipment / accessories like breaker, switches, relays for protection and metering system at both end of utility and consumer Shall have the expertise in the field of UG cabling specifications, laying, termination and inter departmental approval practices Shall have the expertise in utility & consumer portion of 22/33/110/230 KV GIS, Metering & protection standards & requirements of TANGEDCO/TANTRANSCO Shall have the experience in coordination with various utility departments for the enhancement of contract demand Shall have the interest to update on daily basis in monitoring the prevailing state policies and to coordinate with concern departments to ensure the process of availing incentive benefits of state and central statutory entities S/he shall have the adequate knowledge of Grid connectivity network of Tamil Nadu w.r.t 110 KV, 230 KV and 400 KV levels and prevailing practices of connectivity and sourcing practices from utility sources thru each voltage levels respectively. S/he experience in coordinating with offices of Power Utilities, Transco, SLDCs, RE suppliers, Power Traders, Power Exchanges, Power Departments of State, Regulatory Authorities etc. on regular basis. In Renewable Energy Management S/he shall review the monthly energy bills of Power Utilities, Renewable Energy (RE) suppliers and Power Traders of Data Centres in Tamil Nadu. S/he shall have the knowledge of prevailing billing methodology, banking facility and have the knowledge on forecasting & Scheduling S/he shall keep abreast her/himself on Open Access Regulations, Renewable Energy Policies, Tariff Orders of DISCOM/TRANSCO of each state where Company has their Data Centres. S/he shall ensure the timely recovery of the outstanding dues from the customer. S/he shall review and update the power situations in and around the existing data centre campuses and upcoming new sites on regular basis to ensure the stable and reliable supply to the existing DC campuses and future plans Preferred candidate profile Candidate should have knowledge of Power Sector Structure and Grid network in TN and its various stakeholders, Electricity Act, Electricity Rules, Policies, Power Procurement Guidelines etc. Shall have regulatory understanding to summarise orders given by/ of SERCs/APTEL /CERC/High Courts/Supreme Court etc time to time w.r.t. various stakeholders of the power sector. Shall have good understanding of various clauses of Power Purchase Agreements (PPA) and handled power procurement transactions under Bilateral, Group Captive Structure for Thermal power & RE for Commercial & Industrial Consumers including billing, settlement of payments etc. Shall have independently handled the operations of PPAs Shall have experience to deal with DISCOMS, SLDCs, RLDCs, Transco, PGCIL etc. for Open Access clearance under Short, Medium and Long Term Effectively interacted and negotiate with Power suppliers (renewable and non-renewable), Responsible for managing and accurately calculating the monthly power usage pattern and to calculate RE requirements to meet STT GDC Indias short-term ad long-term sustainability targets of respective states Analyse complex problems, prepare and maintain effective MIS and various kinds of other reports & documents Excellent analytical, critical thinking and negotiation skills. Extensive knowledge of the power market industry, particularly aspects related to generation, transmission, distribution, and fuel supply, as well as understanding key energy industry issues, including opportunities, threats and trends. Should be able to evaluate techno-commercial bids of Power suppliers (renewable and non-renewable), Aware of tariff trends of various tenders closed in past by State level (Discoms etc) Good understanding of engineering and economic principles related to Power Sector Ready to work with various stake holders and under Ability to work as a team player and strive to deliver excellent customer services to both internal and external clients. Experience in setting up new electrical substation would be an added advantage Bachelor of Engineering (Electrical Engineering) with MBA will be an added advantage. Minimum 8-10 years of related experience with Power Utility/ Power Generator/Power Trader or with Large Power Consumer. A detail orientation, ability to prioritize work and clearly communicate, lead and drive the team Awareness about the Datacentre business Technical understanding of electrical concepts like Generating Plants, Transmission Lines, Power Distribution, Power Sub-stations, All type of Feeders, HT/LT panels, Associated Electrical Components Good relationship and networking with Power sector stakeholders viz; Renewable Energy Generators, Power Traders, Power Exchanges, Power Utilities, SERCs, etc. Sound ethical and business judgment while demonstrating creative problem solving and professional communications. Perks and benefits

Family Description Legal (LE) covers all legal business matters pertaining to the organisation and acts as advisor on legal issues involving the organisation's government and regulatory compliance. Reviews legal data and advises organisation on appropriate legal action to be taken. Demonstrates experience in general corporate matters, including corporate organisation, securities compliance, drafting transactional documents, license agreements, data privacy, risk management, and contract management. Subfamily Description Corporate, Business & General Law (CBG) comprises the coordinating and managing of all corporate, business, financial, and general legal matters. Impact Impact is primarily short term and and typically functional, departmental or small single geographic in scope through management of resources. Accountable for departmenta/program goals, achievement and cost performance. Actions and errors will normally impact business, program, project, function. Marked contribution to defining the direction for new products, processes, standards or operational plans based upon business strategy. Scope & Contribution Individual Contributor:Independently carrying out consulting, specific functional work within a Business Unit/Geography. Assumes broad perspective. Resolves unique and highly complex problems within own discipline. Makes decisions about own and/or project work using known solutions as basis. Managerial/Supervisory:Typically second (occasionally first) level of solid line management. Effective management of resources and development/implementation of plans and processes. Interprets policies and establishes procedures. Increased awareness and influence of other functions outside of own business area. Decision making often repeated in similar manner - able to choose correct solution or modify existing solution. Innovation Highly independent and self directed. Develops plans, measures effectiveness. Assesses customer relationships and service levels. Can develop and implement complex and innovative concepts. Problems require searching and selecting. Anticipates problems, seeks opportunities. Models creative and innovative work methods. Communication Communicates with parties within and outside of own job function, which may include external customers or vendors depending upon the job function. Requires ability to influence others outside of own job area on policies, practices and procedures. Has cross-cultural knowledge and global mindset. Works to influence others to accept job functions view/practices and agree/accept new concepts, practices, and approaches. Requires influencing others outside of own job area on policies, practices and procedures, e.g. by expressing complex information in an engaging and inspiring manner. Knowledge & Experience Management Experience / Mastery of a specific professional discipline combining deep knowledge of theory and practice within a function. Expert in more than one area, broad perspective. Qualified lawyer with10+ years of relevant experience within a reputable law firm or within multinational companies. Extensive experience in drafting commercial and technology contracts and managing negotiations with customers Excellent academic record and working references / credentials Exceptional communication skills and fluency in English Ability to travel as needed for business needs Experience in IT, technology, or telecommunications industry preferred, but not essential. Excellent legal skills and knowledge of contract, commercial and privacy laws in the region. Highly independent and self-motivated. Influences others to support decisions. Develops and applies innovative approaches to complex or infrequently occurring problems. Demonstrates strategic thinking by anticipating internal/external business issues and developments; uses knowledge to drive improvements. Drive and lead legal support to the Network Infrastructure business in deals including drafting, contract structuring and negotiating with customers/vendors. Act as an advisor for general country legal matters that impact NI business in India, including support to other functions e.g. human resources, finance, corporate services, real estate management etc. Manage and resolve complex contracts and RFP/Tender issues with the customers/vendors. Assist in evaluations and conducting thorough due diligence for all deals and transactions and effectively develop and implement appropriate risk-mitigation strategies in relation to Nokia's business operations. Provide appropriate advice and training to the business/procurement/relevant teams on related contracting matters in line with Nokias policies. Manage customer contracts and provide support to effectively monitor and enforce the contracts from a legal perspective. Evaluate the impact of evolving legal and statutory regulations pertaining to the relevant business function and highlight the same in time and contribute to the business planning process. Maintain good standards of corporate governance, including ensuring compliance with applicable laws, consents, regulations, Company policies and rules

About The Role : The Opportunity Capgemini is seeking a Director-level executive to Lead the fraud consulting practice, defining the strategic vision, goals, and priorities for fraud prevention and detection services. Develop a clear roadmap for driving client success and expanding the firm's presence in the fraud prevention market. Provide guidance on designing and implementing fraud prevention strategies tailored to their needs. Oversee the development and delivery of customized fraud prevention and detection solutions, including risk assessments, fraud risk management frameworks, process improvements, and fraud detection technologies such as AI, machine learning, and data analytics tools. Provide strategic insights and thought leadership on emerging fraud trends, technologies, regulatory requirements, and industry best practices. Identify new business opportunities within existing and prospective clients to support BD efforts. Collaborate with sales teams to create compelling proposals and responses to RFPs, drive the sales cycle and secure new consulting engagements. Lead the development of offers and consulting assets to support pre-sales, GTM pursuits, and capability demonstrations. Primary Skills Our Ideal Candidate He/She/They will have 18-20 years of experience in Financial Crime Compliance & Fraud with deep expertise in key areas such as Anti-Money Laundering, Sanction Screening, Customer Due Diligence, Fraud Detection and Prevention and a strong project track record and demonstrated P&L contribution to sales. 15+ years of experience in fraud prevention, detection, or financial crime consulting, with at least 8 years in a leadership role. Experience in consulting within industries such as banking, insurance, retail, is preferred. He/She/They should be willing to take on a committed engagement role or client-facing advisory/delivery responsibilities while implementing our offers/solutions with our local and/or global teams. A Bachelors or Masters degree in Business Administration, Risk Management, or a related field. Certifications such as Certified Fraud Examiner (CFE), Certified Financial Crime Specialist (CFCS), or similar are strongly preferred. Secondary Skills Additional Responsibilities include: Deep knowledge of fraud prevention and detection techniques, fraud risk management frameworks, data analytics, and fraud detection technologies. Proven ability to design and implement effective fraud prevention programs. Excellent aptitude, problem-solving skills, and quick prototyping / proof -of-concept-creation skills. Exposure to large-scale customer platforms deals/engagements with multinational clients in the market; lead conversations with clients CxOs/VPs of Digital Manufacturing regarding platforms architecture and technology. Work closely with the account team to manage large-scale fraud prevention and detection consulting projects from inception to delivery.

1. Internal Control Development & Maintenance - Develop and implement internal control systems to ensure compliance with regulatory standards and corporate policies. - Establish and maintain operating manuals to guide the company’s processes and operations. 2. SOP & Risk Control Updates - Ensure that all SOPs are timely updated to reflect current processes and risk control metrics. - Regularly review processes to identify any areas for improvement or risk mitigation. 3. Audit Support - Work closely with external and internal auditors to support audits,provide necessary documentation,and resolve any open points or issues identified during audits. - Facilitate periodic reviews and follow-up on audit recommendations to ensure their effective closure. 4. Collaboration with HODs on SOP Updates - Collaborate with Heads of Departments (HODs) to ensure periodic updates and alignment of SOPs across all organizational processes,ensuring they remain relevant and effective. 5. Government Authority Metrics (GAM) Review & Recommendations - Review current government authority metrics (GAM) and recommend changes that could enhance the company’s compliance and operational effectiveness. - Stay updated with any changes in government regulations and advise the organization on necessary adjustments. 6. Process Improvement & Risk Management - Conduct regular reviews of internal processes and controls to identify any inefficiencies or risks,recommending solutions for continuous improvement and better risk management. - Provide recommendations for enhancing internal audit processes to increase transparency and effectiveness.

Are you interested in working in one of the most impactful areas of technology in the world today? Do you want to build generative AI skills while working on a project to transform the most mission-critical IT workloads for organizations that power the global economy? Come join the team that is at the intersection of cutting-edge gen AI and mainframe software development, a key strategic pillar for IBM. As a Gen AI Transformation developer, you will leverage a highly tuned state-of-the-art large language model to transform code from one input source language to another. Role and Responsibilities Analyzing potential areas where non-compliance could occur and proposing mitigation strategies. Creating and updating company policies and procedures to reflect regulatory requirements. Providing compliance training to employees on relevant policies and procedure. Assessing potential security risks and prioritizing mitigation strategies, including PSIRTs and CSIRTs. Develop automation that will improve the reporting, including the creation of dashboards Required education Bachelor's Degree Preferred education Master's Degree Required technical and professional expertise 2+ Years of IT experience. The candidate must have demonstrated: Working knowledge of security concepts including IT security standards, threat modeling, access management, risk analysis. Familiarity with actioning non-compliances, such as vulnerabilities and proposing mitigation strategies Abilities to respond to potential cyber threats through vulnerability scanning, analyzing network traffic, and staying updated on emerging security trends Basic knowledge of security tools Preferred technical and professional experience The candidate should ideally have working knowledge of: Industry regulations and laws to identify potential compliance issues, including: HIPAA, NIST, SOC 2, FISMA, FedRamp, Privacy requirements. Interacting with external agencies to address compliance inquiries and audits. Typical security processes, product lifecycle, penetration testing, architectural diagrams and threat modeling.

Entity :- Accenture Strategy & Consulting Team :- Global Network Data & AI Practice :- Life Sciences Title :- Ind&Func AI Decision Science Manager Job Location :- Delhi, Gurgaon, Mumbai, Bangalore About S&C - Global Network :- Accenture GN's Data & AI (AI Hub India) practice helps our clients grow their business in entirely new ways. Analytics enables our clients to achieve high performance through insights from data - insights that inform better decisions and strengthen customer relationships. From strategy to execution, Accenture works with organizations to develop analytic capabilities - from accessing and reporting on data to predictive modeling to outperform the competition. WHAT'S IN IT FOR YOU? An opportunity to work on high-visibility projects with top Pharma clients around the globe. Potential to Co-create with leaders in strategy, industry experts, enterprise function practitioners, and business intelligence professionals to shape and recommend innovative solutions that leverage emerging technologies. Ability to embed responsible business into everything"from how you service your clients to how you operate as a responsible professional. Personalized training modules to develop your strategy & consulting acumen to grow your skills, industry knowledge, and capabilities. Opportunity to thrive in a culture that is committed to accelerating equality for all. Engage in boundaryless collaboration across the entire organization. Qualifications What you would do in this role Support delivery of small to medium-sized teams to deliver consulting projects for global clients. Responsibilities may include strategy, implementation, process design, and change management for specific modules. Manage daily operations within the team, guide & counsel the team members towards driving the Solution delivery to the Client. Participating in client discussions, developing new industry Point of View (PoV), re-usable assets (tools) Translate complex analytical findings into clear and concise reports and presentations for various stakeholders, including clinicians, executives, and patients (depending on the role). Provide Subject matter expertise in various sub-segments of the LS industry. Develop assets and methodologies, point-of-view, research, or white papers for use by the team and the larger community. Acquire new skills that have utility across industry groups. Support strategies and operating models focused on some business units and assess likely competitive responses. Also, assess implementation readiness and points of greatest impact. Co-lead proposals, and business development efforts and coordinate with other colleagues to create consensus-driven deliverables. Execute a transformational change plan aligned with the clients business strategy and context for change. Engage stakeholders in the change journey and build commitment to change. Make presentations wherever required to a known audience or client on functional aspects of his or her domain. Who are we looking for? Proven experience (10 + years) in working on Life Sciences/Pharma/Healthcare projects and delivering successful outcomes. Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire and analysis, operating model, business process mapping, and so on. Preferably worked with R&D functions such as Laboratory functions (R&D and Quality Check labs), clinical operations and development, decentralized clinical trials, pharmacovigilance, regulatory, quality management system, in capacity of a business analyst or management consultant. Working knowledge of clinical data management platforms such as Medidata/ RAVE, Veeva Clinical suite, pharmacovigilance databases ArisG & ARGUS databases, Regulatory Information Management Systems (Veeva RIM), lab informatics is desirable Leverage ones hands-on experience of working across one or more of these areas such as real-world evidence data, R&D clinical data, and digital marketing data. Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire and analysis, operating model, business process mapping, and so on. Preferably worked with R&D functions such as Laboratory functions (R&D and Quality Check labs), clinical operations and development, decentralized clinical trials, pharmacovigilance, regulatory, quality management system, in capacity of a business analyst or management consultant. Working knowledge of clinical data management platforms such as Medidata/ RAVE, Veeva Clinical suite, pharmacovigilance databases ArisG & ARGUS databases, Regulatory Information Management Systems (Veeva RIM), lab informatics is desirable Excellent analytical and problem-solving skills, with a data-driven mindset. Proficient in Excel, MS Word, PowerPoint, etc. Ability to solve complex business problems and deliver client delight. Strong writing skills to build points of view on current industry trends. Good Client handling skills; able to demonstrate thought leadership & problem-solving skills.

About company: Clariant is a Swiss-based global specialty chemicals company, which is concentrated and developed in three business units: Care Chemicals, Catalysts and Adsorbents & Additives. Our purpose as a company is reflected in our tagline "Greater chemistry - between people and planet", which considers the principles of customer, innovation and people orientation, as well as a focus on creating solutions to foster sustainability in different industries by offering high-value and high-performance chemical specialties. At Clariant, we believe that diversity, equity and inclusion are essential to our success. We strive to cultivate a workplace where all employees feel welcomed, respected, supported, and valued. Our diverse workforce allows us to tap into a wealth of perspectives, experiences, and capabilities that drive innovation. We are committed to ensuring equal opportunities for professional growth and advancement across all levels of the organization, based on objective criteria and regardless of gender, gender identity, race, ethnicity, religion, protected veteran status ,age, disability, sexual orientation or other aspects of diversity in accordance with the relevant governing laws. By bringing together talented individuals with diverse backgrounds and viewpoints, we gain the agility to meet the evolving needs of our global customers and communities. Join our team to help advance our mission of fostering a culture of belonging where everyone can thrive. Purpose of the role: The purpose of role is to integrate environmental, health, and safety considerations into every stage of the product lifecycle, ensuring that products are safe, sustainable, and compliant with regulations, ultimately contributing to the companys overall sustainability goals and reputation Roles & Responsibilities: Ensure timely availability of regulatory compliance information. Monitor regulatory developments and prepare for changes in Clariant systems. Interpret dynamic regulatory requirements and assess their impact on Clariant’s portfolio in collaboration with regions/Bus (Business Units) Provide data for risk and impact assessments. Evaluate, maintain, and archive product safety data in SAP systems. Continuously optimize global processes to enhance efficiency. Oversee smooth Product Stewardship operations. Requirements: Master’s in Science 5+ years of relevant experience in Product Stewardship or in Regulatory Field Experience with SAP EHS (Environment, Health, and Safety) or WINS (Worldwide Information Network System). Must have experience in GHS (Globally Harmonized System), CLP (Classification, Labelling and Packaging), Dangerous Goods, REACH (Registration, Evaluation, Authorisation, and Restriction of Chemicals), etc. Must know how to read all regulations Company Culture: Be part of an amazing team, who will be there to support you. A forward-looking company, with a culture of innovation and a strong portfolio in sustainable technologies. Ongoing Professional Development Opportunities Inclusive Work Environment Approachable Leadership Long term growth opportunity Work-Life Balance Speak Up Culture Women's Inclusion Network of Clariant (WIN) Benefits: Hybrid Work Model- 3 days in office and 2 days remote Child Day Care facility fully sponsored by Clariant In-house Cafeteria & Subsidized meals 30 Days Annual Paid Leaves Clariant-Sponsored Annual Health Check-Up Centralized Company Transport for Designated Routes (Regular shift) Employee Wellbeing & Assistance Program Group Medical Insurance, Group Personal Accident Insurance and Life Insurance Maternity & Parental leave policies Performance-Based Competitive Annual Bonus Plan On-Site Medical Assistance for Employees: Doctor Visits Available Three Days a Week with a Medical Attendant Present Five Days a Week in the Medical Room.

JD - Manager: KEY RESPONSIBILITIES : Expert in business financial models, cash flows for cell, module and wafer manufacturing. Generate insights from industry reports for presentations, analysis and decision making. Compile reports/PPTs/articles etc. on trends & developments in the solar supply chain, key factors affecting it and market research. Ability to liaise on behalf of the company with external parties such as research organisations, industry experts, material suppliers, consultants and other such parties. Well versed with various Central and State incentive schemes for solar manufacturing sector. Should be able to closely monitor the incentive disbursal process. Provide end to end support to corporate finance and investor relations team. Perform other related duties or assignments as desired. EDUCATION : Masters degree in business administration (MBA) preferably from tier-1 B-schools BE / BTech preferably from tier 1 Engineering colleges EXPERIENCE: 5-8 years of prior work experience in strategy and / or business development role. Industry or consulting experience in renewable energy, solar manufacturing sector.

Entity :- Accenture Strategy & Consulting Team :- Global Network Data & AI Practice :- Life Sciences Title :- Ind&Func AI Decision Science Manager Job Location :- Delhi, Gurgaon, Mumbai, Bangalore About S&C - Global Network :- Accenture GN's Data & AI (AI Hub India) practice helps our clients grow their business in entirely new ways. Analytics enables our clients to achieve high performance through insights from data - insights that inform better decisions and strengthen customer relationships. From strategy to execution, Accenture works with organizations to develop analytic capabilities - from accessing and reporting on data to predictive modeling to outperform the competition. WHAT'S IN IT FOR YOU? An opportunity to work on high-visibility projects with top Pharma clients around the globe. Potential to Co-create with leaders in strategy, industry experts, enterprise function practitioners, and business intelligence professionals to shape and recommend innovative solutions that leverage emerging technologies. Ability to embed responsible business into everything"from how you service your clients to how you operate as a responsible professional. Personalized training modules to develop your strategy & consulting acumen to grow your skills, industry knowledge, and capabilities. Opportunity to thrive in a culture that is committed to accelerating equality for all. Engage in boundaryless collaboration across the entire organization. Qualifications What you would do in this role Support delivery of small to medium-sized teams to deliver consulting projects for global clients. Responsibilities may include strategy, implementation, process design, and change management for specific modules. Manage daily operations within the team, guide & counsel the team members towards driving the Solution delivery to the Client. Participating in client discussions, developing new industry Point of View (PoV), re-usable assets (tools) Translate complex analytical findings into clear and concise reports and presentations for various stakeholders, including clinicians, executives, and patients (depending on the role). Provide Subject matter expertise in various sub-segments of the LS industry. Develop assets and methodologies, point-of-view, research, or white papers for use by the team and the larger community. Acquire new skills that have utility across industry groups. Support strategies and operating models focused on some business units and assess likely competitive responses. Also, assess implementation readiness and points of greatest impact. Co-lead proposals, and business development efforts and coordinate with other colleagues to create consensus-driven deliverables. Execute a transformational change plan aligned with the clients business strategy and context for change. Engage stakeholders in the change journey and build commitment to change. Make presentations wherever required to a known audience or client on functional aspects of his or her domain. Who are we looking for? Proven experience (10 + years) in working on Life Sciences/Pharma/Healthcare projects and delivering successful outcomes. Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire and analysis, operating model, business process mapping, and so on. Preferably worked with R&D functions such as Laboratory functions (R&D and Quality Check labs), clinical operations and development, decentralized clinical trials, pharmacovigilance, regulatory, quality management system, in capacity of a business analyst or management consultant. Working knowledge of clinical data management platforms such as Medidata/ RAVE, Veeva Clinical suite, pharmacovigilance databases ArisG & ARGUS databases, Regulatory Information Management Systems (Veeva RIM), lab informatics is desirable Leverage ones hands-on experience of working across one or more of these areas such as real-world evidence data, R&D clinical data, and digital marketing data. Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire and analysis, operating model, business process mapping, and so on. Preferably worked with R&D functions such as Laboratory functions (R&D and Quality Check labs), clinical operations and development, decentralized clinical trials, pharmacovigilance, regulatory, quality management system, in capacity of a business analyst or management consultant. Working knowledge of clinical data management platforms such as Medidata/ RAVE, Veeva Clinical suite, pharmacovigilance databases ArisG & ARGUS databases, Regulatory Information Management Systems (Veeva RIM), lab informatics is desirable Excellent analytical and problem-solving skills, with a data-driven mindset. Proficient in Excel, MS Word, PowerPoint, etc. Ability to solve complex business problems and deliver client delight. Strong writing skills to build points of view on current industry trends. Good Client handling skills; able to demonstrate thought leadership & problem-solving skills. Accenture is an equal opportunities employer and welcomes applications from all sections of society and does not discriminate on grounds of race, religion or belief, ethnic or national origin, disability, age, citizenship, marital, domestic or civil partnership status, sexual orientation, gender identity, or any other basis as protected by applicable law.

Role & responsibilities 1. Raising Order on Suppliers on receipt of Purchase Order from the buyers 2. Raising Indent on the buyers on receipt of Proforma Invoice from the supplier. Follow up with buyers for duly signed Indent & Proforma Invoice for processing the orders. 3. In case of L/C payment terms Following up with the buyers for L/C draft. Scrutinising each & every L/C draft for error free transmission of L/C to avoid amendment charges. 4. Sometimes buyers issues L/Cs directly without approval then check the L/C and get the amendments done (if required) from the buyer immediately to ensure timely shipment. 5. Similarly raising orders on Supplier on receipt of approval from Management. 6. Preparing L/C Annexure, checking L/C Application filled by Accounts team and approving L/C draft on receipt of same from bank. Follow up with the bank for transmission of L/C. 7. Follow-up with suppliers for Ex-Plant details / Shipment schedules and updating the same to the buyers. 8. Once the shipment is effected – Following up with the supplier for N/N docs (Checking N/N docs for error free documentation and requesting supplier for corrections in the docs, if required) & courier details etc. and the same is updated to the buyer. 9. Monitoring day to day activities related to buyer & supplier and resolving issues for smooth clearance of shipments. 10. Co-ordination with the shipping lines & buyer’s CHA for clearance, free detention period issues and any other issues such as container imbalance charges. 11. Maintaining record of all orders placed on suppliers. 12. Preparing Commission statements on monthly basis. 13. Raising Commission Notes on Suppliers on quarterly basis and following up for commission. 14. Maintaining Credit Notes record and following up with the Supplier for the payment. 15. Maintaining DSR Preferred candidate profile Perks and benefits

We're looking for a Product Manager who is passionate about helping organizations meet their compliance and regulatory needs. You have a keen awareness and understanding of the security and compliance market for Cloud Services and IT, while keeping abreast of rapidly evoving compliance frameworks and standards – both globally and regionally. You have smarts to be proactive in identifying compliance gaps and opportunities, planning an optimal roadmap to address improvement opportunities and collaborate with cross-functional teams to deliver on those plans. As a Compliance Product Manager at IBM Cloud, you will create an outcome based roadmap within the framework of IBM Cloud compliance program. You will facilitate the delivery of roadmap elements, and collaborations that facilitate achieving planned compliance outcomes. You’ll join IBM Cloud office in Bangalore, where we collaborate with our development, design and sales team, learn from each other, and build our cloud community. What you’ll do Explore and analyze security, resiliency and compliance priorities for the target market and industries within IBM Cloud Working closely with customers and other market experts to define compliance programs that are needed for their success and also support our business strategy. Develop and articulate a point of view on market opportunity and approach for compliance requirements Develop an optimal roadmap and plan for security, resiliency and compliance programs Lead cross-functional execution against plan to complete compliance programs and ensure go to market enablement and delivery readiness Assess compliance program performance in meeting planned outcomes and address gaps Collaborate with cross-functional teams and multiple stakeholders, including engineering, design, sales, marketing, analysts, ecosystem partners, to achieve compliance objectives Successfully manage compliance program communication from start to completion with minimal oversight Guide entry level product managers and participate in compliance program reviews to convey status and results Demonstrate committed and respectful collaboration between members of cross-functional teams and be part of promoting a positive team culture and work environment Develop expertise on the security and compliance standards and requirements for target market and industries Required education Bachelor's Degree Preferred education Master's Degree Required technical and professional expertise 5+ years experience working in IT Regulatory, Security and Compliance programs such as SOC2, ISO 27001, PCI DSS, NIST SP800-53. HITRUST 5+ years experience working in the Cloud or IT industry. Understanding of cloud platforms and cloud buyer journey, cloud consumption and technology models such as pricing and utilization Understanding of product roadmaps, end-to-end lifecycles, release cadence, and support. Experience in customer-driven usability and hypothesis-driven experimentation A deep passion for innovation and creating data-driven solutions. Excellent communication in English Preferred technical and professional experience 3+ years experience in Product management or equivalent practical experience building or deploying products in a Cloud based software organization Track record of high-quality, self-directed, timely execution, and attention to detail. Technical expertise and ability to communicate, work & build trust with different levels of stakeholders

Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : Regulatory Compliance Good to have skills : NA Minimum 7.5 year(s) of experience is required Educational Qualification : Regular 15 years full time education Project Role :Application Developer Project Role Description :Design, build and configure applications to meet business process and application requirements. Must have Skills :Regulatory ComplianceGood to Have Skills : No Function SpecializationJob Requirements :Key Responsibilities :1 In depth knowledge on Regulatory business processes, content, and data for Life sciences industry2 Prior experience on working on customer facing roles, leading and managing regulatory systems projects and programs3 Experience developing various projects deliverables not limited to current state assessment, RIM strategy and roadmap, high level process maps, BRDs and defining user stories4 Fair understanding on regulatory data flow in and out with various Industry standard boundary system Technical Experience :1 Strong knowledge on various modules of Regulatory systems eg:registration tracking, submissions, publishing ,archiving and reporting 2 Good communications and facilitation skills to organize workshops defining future RIM processes future state, requirements and IDMP data management 3 Prior experience with implementation of at least anyone of the regulatory systems:Generis, Documentum, Ennov Veeva RIM etc Professional Attributes :Good communication skill Educational Qualification:Regular 15 years full time educationAdditional Info : Qualification Regular 15 years full time education

To review validation master plan of the plant and comply with the validation requirements of various regulatory authorities and customers. To review the process validation/ cleaning validation qualification protocols. To review SOPs, batch manufacturing and packing records, specifications, and test methods of the products. To monitor, control and review deviations, change controls, out of specifications may occur at all stages of storage, dispensing, manufacturing, packing, testing and distribution. To ensure issuance, control, distribution, storage, retention and destruction of quality documents and corporate guidelines as per Food safety Quality management system. To ensure that all critical equipment and utilities that are used to manufacture the product are under qualified status, calibrated and are under routine preventive maintenance program. To ensure proper investigation of market / customer / regulatory complaint by root cause analysis, corrective actions and ensure effective implementation of CAPA initiatives, close the complaints, send responses to the complainants, and verify effectiveness of CAPA periodically. To evaluate batch records, COAs and release finished products for sale. To ensure that, all the operations are carried out are as per GMP and laid down procedures, that each production batch complies with the provisions of Food safety standards (FSS) act and other legal, customer and regulatory requirements. To ensure compliance to the regulatory, customer, legal requirements and face audits and comply non-conformities observed during the audits. To ensure compliance to the current ISO 9001, DC Act, FSS Act 2006, FSSC 22000 (including HACCP), FAMI-QS, WHO-GMP and other customer and regulatory requirements. To carry out self inspections and ensure compliance to the audit observations of manufacturing, testing, warehousing facility. To ensure completion of APRs of products and take appropriate actions in case of deviations. Recommendation to recall approving authority on product recall, review, and disposition of recalled and returned goods. Handling of online and in process rejections and take appropriate actions to avoid the recurrences and disposition. To co-ordinate with CQA for up gradation in the SAP systems as per any changes or new product at Mahad site. To monitor stability of products, control sample storage and compilation of analytical reports and take appropriate action in case of failures. To identify and provide resources with co-ordination with other departments to carry out quality functions effectively. To liaison with regulatory authority for new product permissions, licenses and renewals, certificates, and approvals. Ensuring implementation and execution requirements of food regulations for export market (US)-21 CFR Part 110 111. Ensuring avoidance of breach of data integrity at all the levels. Ensuring implementation of effective sanitation activities at all the levels. Imparting required training to shop floor personnel. Adherence to the requirements of EHS norms. To raise the PR for procurement of miscellaneous items, external trainings, certification fees and capex related items. To sign the Excess Material Requisition, LRA notes, BMR return notes and other QMS documents in absence of Head- QA. To perform MSC2N transactions in SAP. Review of Change Control, Deviation, CAPA in trackwise. Implementation and execution of various initiatives as are suggested by corporate functions (SEEDS, Learning university, Quality mindset). SOP, BMR/BPR, layouts, STP review and approval in ENSUR system. To conduct vendor audits for RM/PM. To lead and guide the IPQA team for shopfloor activities. To set, review and evaluate KRA of reportee s. To share the RR nominations of team members on quarterly basis. To identify and implement the OE projects. Patient/ Customer centricity. B. Pharm/ M. Pharm

This position would include the mentioned set of responsibilities but not limited to: Key highlights of the role are listed below (purely indicative and not limiting): Consumer card product and complete life cycle management. Tracking Product profitability, key products parameters tracking and co-ordination with all internal/external stakeholders for driving key interventions. Increasing Market share & profitable growth of the portfolio. SPOC for the Program for multiple departments. Identify, design and implement consumer credit card products for incremental business growth. Manage existing consumer cards and ensure periodic monitoring of key parameters and milestones. Strategic project implementation to offer value added services (VAS) like wallets, scheme related projects, payment mechanisms, RCRL (LE_Upgrade) etc Deliver targeted numbers ensuring the targeted customer and channel mix. Deliver targeted profitability through efficient design and management of product construct, fees and charges Monitor portfolio parameters and work closely with all departments for desired portfolio quality & parameters. Ensure compliance with regulatory and industry requirements at all times. Manage all internal/external stakeholders including but not limited to Sales, Marketing, Operations, Customer Service, Finance, IT, Risk and Collections Applicants should possess the following attributes: • Passion, Curiosity and interest to learn the entire Credit Card Business • Experience in Credit Card product and portfolio management. (Most Important 2 pointers) • Experience in managing cobrands or strategic alliances. • Exposure to Credit Card technology including issuance as well as merchant acquiring. • Understanding of Indian Credit Card Industry and Regulations governing it. • Strong business development and relationship skills • Commercial skills, negotiation skills and domain expertise • Product thinking, Problem solving, Strategic Orientation • Tech Understanding, Hustle, Collaboration Skills • Analytical Ability, Business Understanding, Marketing

Skill required: Control Testing - Agile testing Designation: Regulatory Compliance Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years What would you do? Accenture is looking for experienced control testers primarily for their Risk & Compliance vertical. Looking for someone how has sound knowledge of banking and its product. Understanding of Regulatory Control Frameworks and guidance. Working knowledge of data reporting tool is plusLooking for someone with Operational and SOX testing experience.Conduct testing tasks within Agile models and integration processes and manage development sprints. What are we looking for? We are looking for candidates who has an eye for detailsUnderstanding the audit, control & compliance function Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualifications Any Graduation