Job Title: Manager or Sr. Manager - Compliance Location: Mumbai Summary of Key Responsibilities : We are looking for a candidate at Manager or Sr. Manager level. Responsibilities include providing overall assistance in reviewing sales, marketing and commercial activities to ensure that they are compliant with the company policies and applicable legal, regulatory requirements and also review and monitoring of business activities and document review. Area of Responsibility: Compliance: Supports the business with a view to have all processes and transactions performed in accordance with the organization policies, procedures and applicable legal, regulatory requirements. Provides advice / guidance in the areas of marketing activities of a pharmaceutical company (Interaction with HCPs and HCI s) to the business teams. Support the development of a corporate culture where ethical and compliant values-based behavior is embraced by employees, helps the management to deliver the right tone from the top Support project teams in implementing cross functional ethics and compliance initiatives to include corrective and preventive measures Contribute to the development, review and implementation of the policies, SOP s and guidelines as required on time to time basis. Monitoring/Audit/ Review Review compliance controls for existing processes in business practices and suggest corrective action plans Execute Monitoring/ Review as per Monitoring plan and ensure timely closure. Monitor the performance of Compliance program / activities on a continuous basis. Conduct periodic reviews of documentation and transaction audits and remedial action measures. Ensure proper documentation before commencement of activities and proof of closure Maintenance of documentation/ record of Monitoring activities Partner with relevant departments to follow up with respective functions for mitigation plan execution and ensure implementation of corrective actions Prepare / Assist with p periodic reports and data analysis to /for relevant stakeholders Training/Awareness : Create awareness and conduct knowledge sharing sessions, training on compliance related topics and maintain records in relation thereto. Train / Mentor Business Compliance Executives / Analysts on Job Position requires national travel Qualification: Atleast 10 years of total previous work experience minimum 5+ years of relevant experience in compliance or legal Preference in Pharmaceutical Industry Familiarity with UCPMP and Local Pharmaceutical related laws and regulations in India

Job Title: Senior Executive Job Grade: G11B Department: NAM Quality Cluster Location: Vadodara Job Summary This position shall be responsible for Preparation of quarterly report to be sent to FDA for CD copies sent to vendors and employees. Management of new material codes creation in MDO Fuse portal for Quality and R&D functions. Management of GMP consultants travel arrangement for visiting Sun Pharma India sites, including review/verification and payment processing of consultants invoices. Area Of Responsibility Prepare quarterly report to be sent to FDA for CD copies sent to vendors and employees. Creation of new material codes creation for ZLAB items in MDO Fuse portal for Quality and R&D functions. Management of GMP consultants travel arrangement for visiting Sun Pharma India sites, including review/verification and timely payment processing of consultant’s invoices. Coordinate with site for site review of GMP consultant’s invoices and get site and Global Quality and Compliance Head approvals for the same Coordinate with commercial/finance team for preparation of PR/PO/GRN for the consultants’ invoices and timely payment processing. New Material codes creation management for ZLAB items in MDO Fuse portal for Quality and R&D functions. Any additional work assigned by the reporting manager to support North America Cluster. Work Conditions: Corporate Office Environment Travel Estimate Up to 10 % Education and Job Qualification A minimum of a Master’s degree in Commerce or relevant scientific field is required. A minimum of 8+ years of experience in a pharmaceutical industry with good exposure in Procurement/Finance/Quality is required. Strong knowledge of commerce, import/export management is essential. Good organizational, interpersonal and communication skills are essential. Excellent interpersonal skills and ability to communicate effectively with middle management levels of the organization and external stakeholders Expertise in software applications such as: MS Word, MS Excel, MS Office, Windows, PowerPoint, Microsoft Outlook, Code Creation, SAP-HANA etc. Experience A minimum of 8+ years of experience in a pharmaceutical industry with good exposure in Procurement/Finance/ Quality is required. Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Position: Manager Investigation Lead (OSD) Function: Production Sub-function: Lead Investigation of UPD/OOS/OOT Location: Halol-II Tablet Department Areas of Responsibility JOB DESCRIPTION: He is accountable for COE (Centre of Excellence) related activities. He is accountable for daily activity (as a Manager) : Overall responsible for production and packing activities related to Tablet, Soft Shell &Gel department. Responsible for the day to day production functions in production. Establishing new procedures, maintaining and updating existing procedures in the Tablet, Soft Shell& Gel department. To assist establishing a system in accordance with Good Manufacturing Practice guidelines and Responsible for follow established procedures, maintaining and updating existing procedures department. Updation Approval and Execution of BMR, SOP, Protocol and other GMP documents. Preparation of daily reports to production manager / superiors on day to day activities concerning the department. Coordination with other departments like Administration, Warehouse, Quality Control, Quality Assurance, Quality Engineering, MIS and Engineering for related activities. Responsible to co-maintain, coordinate for validation and GMP in all departments along with the Quality Assurance officer and to co- ordinate with Quality control department in matters relating to product quality. Train the subordinates and manpower to meet the organizational goals and achieve GMP compliance. Optimization of resources namely men, material and machine in respective department. Help the officers/ subordinates into standardize production activities to achieve better efficiency and product quality. Responsible for Calibration, Qualification and Validation activity of respective Equipments or Product. Responsible for Production Planning, schedule, control and execution, E-log / Ample Logic Execution. Approval of Job Responsibility & Indent. Responsible for investigation preparation and approval in trackwise. Initiator, Review & approval in Track wise, Medhas Module, EDMS, SAP, LMS module access. Responsible to perform the internal audit as auditor. Responsible for preparation / review of Risk assessment for New / Existing product, Evaluation and Approval. Responsible for Activity of Rejection / Reprocessing based on Corrective actions of Investigation. Destruction note review and approval. Responsible for Effective Compliance of Regulatory Observation, its Report documentation & Approval. Procurement of machineries, change parts, spares and material required in respective department. Any other job assigned by the superior. Also responsible for carrying out any other responsibilities assigned by superior from time to time orally or in writing. Educational Qualification : B Pharmacy/M Pharmacy Skills : Good Writing Skill on UPD/OOS/OOT Experience : 15 to 18 Yrs

Responsibilities Responsible for Downstream activities in Bulk Manufacturing/production facility. Role: 1. Ensure Facility monitoring, readiness, maintenance, equipment operations like Mixing vessels, TFF systems, AKTA systems, buffer preparation, chromatography techniques, autoclave operations, and coming in shifts basis for involving & supporting in continuous manufacturing of biological products at Bulk Manufacturing (BM) /production facility. 2. Operate the Autoclave and DHS activities 3. Tracking of inventory of process raw materials & consumables used in manufacturing. 4. To understand and follow the safety practices and usage of PPEs in Bulk Manufacturing facility and during process. 5. Execution of Scale up of Development batches in Bulk Manufacturing facility with coordination of R&D support. 6. Coordination with engineering department and external vendor on tracking and completion of preventive maintenance/calibrations activities of Downstream process Equipment and instruments. 7. Follow good documentation practices (GDP) such as online documentation and ensuring cGMP compliance in downstream process and facility operations. 8. Coordination with stake holders and Involve in technical trainings, safety trainings related activities for smooth functioning in production facility.

Role & responsibilities :- Job Summary : Regulatory submission of new products, variations, response to queries, Life cycle management for US and OAM region through preparation of quality dossiers enabling timely approvals. Area Of Responsibility 1. New submissions: a. Review & prepare CMC (Chemistry, Manufacturing and Controls) dossiers for fresh submissions. b. Review documents (Development report, scale up report, specification, stability protocol, analytical validation), etc. Before initiation of Exhibit batches for adequacy. 2. Approval : Review & prepare response to deficiency enabling approval of products filed to regulatory agency. 3. Lifecycle management for drug formulations : a. Prepare and review variation , Annual notification and labelling approval for US and OAM b. Review of change control and file variation as per country requirement 4. Regulatory compliance: a. eCTD compilation b. Ensure reposition of comprehensive product information into central repository C. Review regulatory filing impact of variations, change controls, etc

Job Role : ODR Auditor Designation : Manager (G11A)/Sr. Executive ODR Department & Sub Area (If applicable) : Office of Data Reliability (Mohali) Accountabilities: This position is accountable for critically reviewing any data and documents generated in Quality Control Laboratory as well as executed Batch records which are meant for submission to USFDA and ensure the data integrity and accuracy of all documents ready for submission. Ensure during pre-submission review of all data pertaining to submission to USFDA that all Finished products, Drug Substances, Intermediates, Raw materials and Packaging materials are tested as per approved procedures under cGMP conditions and documented precisely in raw data sheet or respective Lab notebooks. Responsibility: Perform thorough review of raw data (meant for filings to USFDA) compiled & already reviewed/approved by QC analytical data reviewers and QA and ensures the accuracy, completeness and integrity of data/document meant for regulatory submission to USFDA. Thorough review of executed Batch Records (meant for filings to USFDA) which are already reviewed and approved by QA and ensure the accuracy, completeness and integrity of data/document meant for regulatory submission to USFDA. Review of supporting documents like user log books, attendance records & electronic data, if any, (related to documents/data meant for USFDA submission) viz-a-viz the activities with executed documents prepared by quality control as well as manufacturing/packaging activities reported in executed BPRs. During review, ensure the compliance of employee Certification for all documents (analytical and manufacturing) intended for USFDA regulatory submission. Critically review the Analytical and Mfg. deviations (if any) during pre-submission review of documents/data related to filing for USFDA. To scan, review, and load the documents/data in Laserfiche and promote to ODR Manager with audit worksheet. Documentation of pre-submission audit worksheets (loaded in Laserfiche) of the product. Any other responsibilities which are appropriate and/or assigned by the department head. Education and Job Qualification: Minimum of a Bachelor degree in Pharmacy, Chemistry or related field. Experience: 08-12 years Industry: Pharmaceutical Experience: Experience in analytical laboratory having handled the latest analytical instruments Knowledge of GxP, cGMP and regulatory requirements ICH / USFDA guidelines Knowledge of QC Laboratory test procedures, Method validation, and Analytical method Transfers, API & Finished Products testing procedures and Stability testing procedures. Strong skill to review the Laboratory data including data in electronic format

Job Role : ODR Auditor Designation : Manager (G11A)/Sr. Executive ODR Department & Sub Area (If applicable) : Office of Data Reliability (Gurugram) Accountabilities: This position is accountable for critically reviewing data and documents generated by Analytical Research Department and Product/Packaging development department which are meant for submission to USFDA and ensure the data integrity and accuracy of all documents ready for submission. Responsibility: Perform thorough review of raw data (pertaining to R&D related activities (viz. Analytical Method Validations /Analytical reports / Analytical Method Transfer / Product Development Report etc. ) compiled by respective department & already reviewed/approved by R&D Quality/QA and ensure the accuracy, completeness and integrity of data/document meant for regulatory submission to USFDA. Review of supporting documents like user log books, attendance records & electronic data, if any, (related to documents/data meant for USFDA submission). During review, ensure the compliance of employee Certification for all documents (R&D related data) intended for USFDA regulatory submission. Coordinating with stakeholders (Regulatory affairs, Analytical research & Product/Packaging development research etc. ) for raw data for ODR review. Critically review R&D related deviations (if any) during pre-submission review of documents/data related to filing for USFDA. Audit the pre-submission data and report any non-compliance activities to immediate Manager. Documentation of pre-submission audit checklists and worksheets of the product. To scan, review, and load the documents/data in Laserfiche and promote to ODR Manager with audit checklists and worksheets. Any other responsibilities which are appropriate and/or assigned by the department head. Education and Job Qualification: Minimum of a Bachelor degree in Pharmacy, Chemistry or related field. Experience: 08-12 years Industry: Pharmaceutical Experience: Experience in analytical laboratory having handled the latest analytical instruments Knowledge of GxP, cGMP and regulatory requirements ICH / USFDA guidelines Knowledge of QC Laboratory test procedures, Method validation, and Analytical method Transfers, API & Finished Products testing procedures and Stability testing procedures. Strong skill to review the Laboratory data including data in electronic format

Role & responsibilities Job Summary : Regulatory submission of new products, variations, response to queries, Life cycle management for US and OAM region through preparation of quality dossiers enabling timely approvals. Area Of Responsibility 1. New submissions: a. Review & prepare CMC (Chemistry, Manufacturing and Controls) dossiers for fresh submissions. b. Review documents (Development report, scale up report, specification, stability protocol, analytical validation), etc. Before initiation of Exhibit batches for adequacy. 2. Approval : Review & prepare response to deficiency enabling approval of products filed to regulatory agency. 3. Lifecycle management for drug formulations : a. Prepare and review variation , Annual notification and labelling approval for US and OAM b. Review of change control and file variation as per country requirement 4. Regulatory compliance: a. eCTD compilation b. Ensure reposition of comprehensive product information into central repository C. Review regulatory filing impact of variations, change controls, etc Note:- We are specifically looking for professionals with prior experience in US/EU Market.

Role & responsibilities 1. To ensure GMP compliance on shop floor. 2. To follow SOPS and policies and perform tasks as per the SOP. 3. To perform investigation along with CFT to identify the root cause. 4. To participate in the preparation and review of investigation report for OOS, OOT, product quality complaints and unplanned deviations related to manufacturing. 5. To initiate change controls, planned deviations and unplanned deviations related to production department. 6. To provide the awareness training and SOP related trainings to concern personnel. 7. To develop skills in subordinates by motivation and on the job training. 8. To coordinate with internal and external auditor along with CFT. 9. Drafting of investigation for OOS, OOT, product quality complaints and unplanned deviations related to manufacturing. To prepare review and timely compliance of audit related observations of production department . Preferred candidate profile B.Pharma / M.Pharma candidate having regulatory exposure of handling QMS systems in pharma industry and sound knowledge technical knowledge as well as good communication skills. candidate must possess 5 to 10 yrs experience in handling QMS process and must have worked in the past in Quality/Manufacturing function.

Hi, We are having an opening for Manager IT -R&D (overseas sites) Job Summary: Shall be responsible to manage the overall IT Portfolio at overseas R&D sites (Haifa, Brampton, Terapia). The role requires a deep understanding of regulations and compliance. The manager will be responsible to prepare and monitor annual budget. Partnering with various stakeholders is one of the key responsibilities. Role and Responsibilities Management of projects and IT portfolio at overseas R&D sites Closely working with ITBP for these R&D sites Identify required IT initiatives for the sites and responsible for implementing the right identified solution Liaison with various internal IT stakeholders to deliver solutions for these sites Identify IT budget requirements, monitors and controls project budgets, ensuring financial objectives are met Identifies and resolves issues, escalating when necessary Provides regular updates to leadership and stakeholders about ongoing projects and activities Support in implementation of GDO applications Qualifications and Preference Qualifications Bachelor's degree in Information Technology, or Computer Science or related field or Post Graduation in Science stream Minimum of 5-7 years of experience in managing IT portfolio, preferably Pharma/ Life Sciences domain Ability to manage multiple tasks and projects simultaneously. Strong analytical and problem-solving skills. Excellent communication and interpersonal skills. Sensitive and knowledgeable about language and culture preferences of overseas sites. Stakeholder communication and management Risk analysis and mitigation Ensure project strategic alignment to ensure project goals are delivered Preferred Qualifications Advanced degree in Life Sciences, Information Technology, PMP or a related field. Project, budget and resource management experience Deep understanding and experience of project implementation Familiarity with laboratory instruments and software Problem solving skills Conflict Management

Hi, We are having an opening for Senior Manager R&D IT at our Baroda location. Job Summary : The Senior Manager will play a role of Lead IT for R&D Baroda. Lead will be responsible to manage team and multiple projects simultaneously, ensuring alignment with organizational goals, and oversees timelines, budgets, and risk management. As a Lead, shall be responsible to present IT in different forums like Quality MRM (Monthly Review Meeting), Quality observation groups etc., Lead will also be responsible to partner with cross-functional and leadership team. Role and Responsibilities: Program Planning and Execution - Develops and executes project plans, budgets, resources, and deliverables. • Stakeholder Management Interacts with internal and external stakeholders • Risk Management - Identifies, assesses, and mitigates project risks, ensuring successful outcomes. • Budget Management Identify IT budget requirements, monitors and controls project budgets, ensuring financial objectives are met. • Team Leadership - Leads and manages the team by fostering collaboration and effective communication. • Problem Solving - Identifies and resolves issues, escalating when necessary. • Reporting and Communication - Provides regular updates to leadership and stakeholders about ongoing projects and activities Qualifications and Preference Qualifications Bachelor's degree in Information Technology, or Computer Science or related field or Post Graduation in Science/IT stream Minimum of 8-10 years of experience in managing IT portfolio, preferably Pharma/ Life Sciences domain Ability to manage multiple tasks and projects simultaneously. Strong analytical and problem-solving skills Team handling and management experience Excellent communication and interpersonal skills. Stakeholder communication and management Risk analysis and mitigation Ensure project strategic alignment to ensure project goals are delivered Preferred Qualifications Advanced degree in Life Sciences, Information Technology, PMP or a related field. Project, budget and resource management experience Deep understanding and experience of project implementation Familiarity with laboratory instruments and software Problem solving skills Conflict Management

Hi, We are having an opening for R&D-IT Manager-ELN at our Baroda location. Job Summary : R&D-IT Manager will be responsible for the successful implementation of assigned projects. This role requires a strong technical skills and deep compliance understanding of R&D and Lab procedures and processes and the ability to work closely with cross-functional teams to ensure IT applications are running successfully. Experience in ELN implementation is preferred. Role and Responsibilities : ELN implementation for R&D Functions NuGenesis SDMS platform upgrade implementation Implementation of PMS- Store Inventory & Equipment inventory Computer System Validation of scientific software and instrument software Managing and closure of assigned QMS within the timelines Application support for Regulatory information management project Implementation support, testing and documentation of ongoing projects at R&D Baroda site Responsible to face internal/external audits and draft audit response, as needed Qualifications and Preference Qualifications Bachelor's degree in Information Technology, or Computer Science or related field. Minimum of 5-7 years of experience in application support, preferably Pharma/ life sciences domain Ability to manage multiple tasks and projects simultaneously. Strong analytical and problem-solving skills. Excellent communication and interpersonal skills. Preferred Qualifications Familiarity with laboratory instruments and software ELN implementation experience Good documentation skills to create and manage GxP documents Project Management skills

Hi, We are having an opening for Executive/Sr. Executive- R&D IT at our Gurgaon location Job Summary : R&D-IT Executive/Sr. Executive will be responsible for supporting IT applications, managing QMS across R&D Gurgaon functions. The person should have a strong understanding of CSV. The role requires a good understanding and experience in R&D/Lab policies and procedures to ensure applications/QMS are comply as per the applicable regulation. Job Description : Role and Responsibilities Application support for R&D applications (PMS, NuGenesis, Empower, Amplexor etc.) Managing and closure of assigned QMS within the timelines Application implementation support, testing and documentation of ongoing assigned projects Helping and providing IT support to business users during Performance Qualification phase Perform miscellaneous job-related duties as assigned Qualifications Bachelor's degree in Information Technology, or Computer Science or related field. Minimum of 3-5 years of experience in application support, preferably Pharma/ life sciences domain Strong understanding of CSV Software Development Life Cycle Preferred Qualifications Experience in NuGenesis and Empower is preferred Good documentation skills to create and manage GxP documents

Hi, We are having an opening for Manager IT-Project support for our Gurgaon Location. Job Summary : Application support and lead will be responsible for the successful implementation of assigned projects. This role requires a deep understanding of Argus application and Pharmacovigilance area. Understanding in AI/ML, Artwork management is preferred. Job Description : Role and Responsibilities Argus upgrade application implementation support for PVG department AMS (Artwork Management System) upgrade and enhancements Support in AI/ML initiatives Execute the tasks defined in project plans, adhering to timelines, for successful implementation of assigned projects and activities Managing QMS Shall support internal/external audits and draft audit response, as needed Qualifications and Preference Qualifications Bachelor's degree in Information Technology, or Computer Science or related field. Minimum of 5-7 years of experience in application support, preferably PVG domain Ability to manage multiple tasks and projects simultaneously. Strong analytical and problem-solving skills. Excellent communication and interpersonal skills. Preferred Qualifications AI/ML development Oracle Argus Data processing and engineering Troubleshooting and problem-solving Familiarity with Big Data Technologies Performing Statistical Analysis

1. Characterization of RLD pack samples. 2. Finalization of packing configuration for Exhibit batch packing of new generic product/NDA as per requirement. 3. Identification of new packaging material & new vendor development for packaging materials. 4. Mold development for primary packaging material & secondary packaging material & its validation. 5. Support to Regulatory team on ANDA s/NDA s filling for regulated market. 6. Coordination with NPI & planning team for launch of ANDA s/NDA s. 7. Preparation & revision of packaging material specification. 8. Preparation & review of MPC, FMEA, TA, DHF & AFMEA. 9. Preparation & review of Development Study protocol & report & execute the study. 10. Performing functional test as per regulatory requirement. 11. Coordination with Cross functional team like (FDD/RA/Plant/Marketing/PMO) for completion of task. 12. Participating in FAT of machines. 13. Support to plant for validation, trouble shooting and market complaints. 14. SOP preparation, periodic review and packaging lab equipment handling/maintain calibration records. 15. Preparation of Packaging documentation (Pack Style, Justification Report etc. as per Product/Regulatory) as required. 16. Handling of primary and secondary packaging material in storage area & maintaining the PM quantity for stability packaging at R&D.

Key Responsibilities Overview management of Medical Devices development process as per specific product requirements and in line with respective country regulatory guidance Generate technical documentation for the product Design History file and Device Master Records as per specific country regulatory guidance To support Business in identifying New technologies /Device manufacturing partners and in evaluation of patents Designing and Development of assembling and in-process testing machines To Partner with Manufacturing ,Engineering /Projects , Quality team to ensure that the transition of products through R&D , Product approval and manufacturing scale up are smooth , timely and cost effective To provide quality engineering support to commercial Medical Devices Key Competencies and Attributes Demonstrable Detailed working knowledge of Medical Device Industry Complete understanding of Drug Device Combination Products guidelines of specific countries Thorough knowledge in various ISO s related to Medical Device Development , inprocess testing Knowledge on Human Factor Testing and statistical analysis of data Knowledge on various manufacturing and assembling process of Medical Devices including materials used in manufacturing of Medical Devices Ability to establish good network in developing and execution of Medical Device Projects Application knowledge of design control principles, statistics, process & systems validation, and quality engineering techniques to positively influence projects and manufacturing. Ability to utilizes quality tools to include Risk analysis FMEA, statistical techniques including six-sigma and DOE (design of experiments), root case analysis, reading and correcting drawings. Technical knowledge to navigate complex agency regulations of FDA & QSR requirements and guidance under 21 CFR820, ISO13485 and ISO14971. Should be creative , continually learning and exploring new ideas Good team player who works well in a team with strong interpersonal skills , a demonstrated ability to influence his/her peers Displays highest level of integrity and confidentiality

Designing, executing and interpreting bioassays/pharmacological studies. Knowledge of GLP/GMP. Leading and managing in-vitro/in-vivo projects, ensuring timely completion Mentoring junior scientists, building and leading cross functional teams Analyzing data, preparing reports and presenting to stakeholders Collaborating with other departments, to advance progress of projects

Designing, executing and interpreting bioassays/pharmacological studies. Knowledge of GLP/GMP. Leading and managing in-vitro/in-vivo projects, ensuring timely completion Mentoring junior scientists, building and leading cross functional teams Analyzing data, preparing reports and presenting to stakeholders Collaborating with other departments, to advance progress of projects

Histopathology evaluation and report preparation of pharmacology studies Planning, designing and monitoring of GLP/Non -GLP toxicity studies in rodent and non-rodent Scientific data collection, interpretation of toxicology data and study report preparation/review.

Hi, We are having an opening for Manager IT-Digital Marketing Lead at our Mumbai location. Job Summary : Desired Skills & Experience Candidate should have worked on end-to-end Digital marketing Tech stack for a consumer business, preferably as a team lead, and having experience of handling multiple partners and agencies. Minimum of 8-10 years of experience in a full cycle implementation as well as in support projects. Varied experience in different domains of Digital marketing like SEO, SCM, Google Analytics, email, whatsapp and sms marketing etc Should have demonstrated exemplary performance in driving website traffic, brand awareness, digital footfall, lead generation and revenue growth Candidates with hands on experiences in Customer Engagement Platforms like WebEngage, CleverTap etc. Demonstrated track record for maintenance and upliftment of digital assets and content management in an MNC or matrixed organization Should have worked in cross functional setup, with multiple stakeholders across IT, Sales & Marketing Preferred experience in other allied ATL modes of communication and technical systems Proficiency in latest and appropriate Cloud and AI/ML services and offerings Areas Of Responsibility: Roles & Responsibilities * End to end ownership of implementation, uptime and maintenance of all digital marketing assets, including content management * Provide consultative support and execute new tech initiatives to support marketing strategies of brand awareness and customer acquisitions * Facilitate the implementation and support of new Digital Marketing strategies from the IT side * Perform detailed analysis of complex business process requirements and provide appropriate system solutions; identify, interpret, validate and document customer requirements. * Facilitate workshops to collect business requirements. * Map client business requirements, processes and objectives; develops necessary product modifications to satisfy customers needs. * Design, customize, configure and testing of the digital marketing assets * Identify gaps, issues and work around solutions. * Act as liaison with internal customer for troubleshooting: investigate, analyze, and solve software problems. * Handle changes or emergency transports as needed for high priority issues; Document functional designs, test cases and results. * Proactively identify and propose business process and/or system enhancements. * Provide consulting services on both new implementations and existing support projects. * Act as a liaison between the business functions and the technical team. * Provide ad-hoc training and user support as required help in upskilling of both IT and Business users by fostering awareness of new age technology and platforms * Work self-directed and independently; may act as subject matter mentor to more junior members. Educational Qualification : BE/ BTECH/MBA Specific Certification : Digital Marketing specialization, Google Analytics Experience : Min. 8 to 10 Years in Digital Marketing