Summary
Overview
Work History
Education
Skills
Certification
Timeline
Generic

Sreekanth Pagadala

Bridgewater,NJ

Summary

Qualified [Desired Position] with solid background in managing business operations. Leveraged expertise to streamline processes and enhance operational efficiency, contributing to overall business growth. Demonstrated leadership and problem-solving skills to effectively manage teams and ensure seamless operations.

Results-driven business professional with proven track record in business operations management. Skilled in optimizing workflows and improving operational effectiveness. Known for fostering collaboration and achieving consistent results through adaptive strategies and reliable team support.

Experienced with optimizing business operations to achieve maximum efficiency and productivity. Utilizes strategic planning and process improvement to drive operational success. Strong understanding of leadership principles and effective team management to sustain business growth.

Professional Business Operator with strong focus on operational efficiency and strategic management. Proven track record of leading teams to achieve business goals and adapting to evolving challenges. Expertise in process optimization, financial oversight, and stakeholder communication. Known for collaborative spirit and reliability in high-pressure environments.

Seasoned management professional successful at establishing excellent working relationships with customers, employees, vendors and contractors.

Astute Business Operations Manager focused on supporting cross-functional teams to increase customer satisfaction through process improvements. Respectful and respected professional with exceptional knowledge of developing strategic plans for service excellence.

Strong leader and problem-solver dedicated to streamlining operations to decrease costs and promote organizational efficiency. Uses independent decision-making skills and sound judgment to positively impact company success.

Encouraging manager and analytical problem-solver with talents for team building, leading and motivating, as well as excellent customer relations aptitude and relationship-building skills. Proficient in using independent decision-making skills and sound judgment to positively impact company success. Dedicated to applying training, monitoring and morale-building abilities to enhance employee engagement and boost performance.

Collaborative leader partners with coworkers to promote engaged, empowering work culture. Documented strengths in building and maintaining relationships with diverse range of stakeholders in dynamic, fast-paced settings.

Dedicated [Industry] professional with a history of meeting company goals utilizing consistent and organized practices. Skilled in working under pressure and adapting to new situations and challenges to best enhance the organizational brand.

Overview

20
20
years of professional experience
1
1
Certification

Work History

Business Operator

Amgen
04.2024 - Current
  • Individual award for delivering 6 SI sub-projects in a stringent timeline in Henkel project and recognized by CFO
  • Won the “Value Creator” Excellence award for delivering change controls with zero defects for
  • Wyeth client consistently
  • Won the “Business Operator” Excellence award for driving the Henkel application support consistently to >95% SLA
  • Submitted an evaluation document between 2 ECM products “EMC Documentum” and “Vignette” which will be used as quick reference to do product fitment analysis of new projects
  • Recognized and rewarded for timely completion of project with meeting deadlines/ milestones in AstraZeneca, Henkel, Pfizer, Cabot, Merck and AbbVie projects
  • Recognized Business Operator award in 2018, 2019 in Allergan project., is world’s largest independent bio and technology company to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer
  • Amgen discover, develop, manufacture and deliver innovative medicines to help millions of patients and leverages most of the modules of Veeva like Veeva Quality Docs, Veeva eTMF, Veeva RIM, Veeva CTMS, MedComms and Promomats
  • In the current project Amgen acquired a company called Horizon
  • Amgen wants to migrate the data from Legacy Horizon system into Amgen RIM system with the help of Cognizant by analyzing the data, object model from source systems to target RIM system via phases wise
  • Responsibilities:
  • As a migration specialist analyze the Horizon RIM system data and work with the BA/ Project lead to identify the scope for each wave
  • Analyze the requirements and schedule a meeting with business and Technical POCs to clarify the queries on regular basis
  • Define the mapping specifications and rules and reviewed by business related to the Regulatory, Promotional and FDA 356h Submissions
  • Discuss the data enrichment fields with business on the needed input and assist with fillign the mapping specifications within the timeline
  • Create a change in Service Now and review it with the validation team, Technical and business owner
  • Guide the offshore team with mapping specification update and data verification for accuracy
  • Export the submission archive content and copy to the staging location to migrate the data into Amgen RIM
  • Create Configurations like Regulatory Objectives, Product families, Applications and the picklist values needed in the Amgen RIM
  • Define and draft the IQ and UAT scripts in the ALM system and drive the meetings to review the scripts by Validation and technical teams
  • Update the regular and weekly status to Project Manager to prepare the decks to the Stake holders.

Developer, Specialist

Cognizant Technology Solutions, Amgen
04.2024 - Current
  • Client Amgen
  • Tools/ Technology Vault MedComms Scrum framework, Enterprise Architecture
  • Team Size 2 (Onshore), 5 (Offshore)
  • Role Veeva, is world’s largest independent bio and technology company to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer
  • Amgen discover, develop, manufacture and deliver innovative medicines to help millions of patients and leverages most of the modules of Veeva like Veeva Quality Docs, Veeva eTMF, Veeva RIM, Veeva CTMS, MedComms and Promomats
  • Veeva Vault MedComms is a regulated content management application that supports unique content types, lifecycles, and workflows specific to the needs of Medical Affairs
  • It enables content creation, review and approval, storage, management, and distribution
  • MedComms is connected to CRM for automatic distribution of medical content via applications like CLM and Approved Email
  • The MedComms API enables integration with third-party systems
  • Responsibilities:
  • Participate in requirements gathering efforts for the Veeva applications
  • As a developer, responsible for handling assigned JIRA items related to MedComms
  • These items are developed, tested, and moved to production according to the defined sprint timelines
  • Responsible for implementing configuration change requests related to lifecycles, workflows
  • Security settings, objects and document type/subtypes
  • Responsible for creating the security policies and create service accounts to other integrated systems like Veeva CRM
  • Setting up the new products, Review Teams in support of Promomats to MedComms integration as per business request
  • Configure the jobs as per business requirements and scheduling them to run on configured intervals
  • Create reports, report types, flash reports and export them into preconfigured excel
  • Implement the integration and trouble shoot the issues related to MedComms to ALIGN/ CLM applications
  • Troubleshoot and publish the documents from Promomats to MedComms by fixing the issues
  • Update the object types, restricting the fields based on roles in support to CLM publishing
  • Create technical/ functional documents and reviewed by client/business
  • Create and execute the Change requests by ensuring that all the deliverables and processes are met
  • Work with the integration teams SAM, Tableau reports for any integration issues and fixing them collaborating with the teams
  • Creating user accounts, DACs and updating the documentation on regular basis
  • Project, 2:
  • Organization: Cognizant Technology, Title Horizon to Veeva RIM migration
  • Client, Tools/ Technology Veeva RIM, Quality Docs, Agile Project management, Enterprise Architecture
  • Team Size 1 (Onshore), 3 (Offshore)
  • Role Veeva Migration

Technical Lead

Cognizant Technology Solutions, Veeva
05.2023 - 03.2024
  • Vault
  • Client AbbVie
  • Tools/ Technology Veeva Quality Docs, Veeva SDK, REST API, VQL, Java Spring boot, Agile Project management, Enterprise Architecture, Size 4 (Application Offshore), 1 (Onshore)
  • Role, AbbVie is an American Pharmaceutical company head quartered in North Chicago, Illinois
  • The company decided to migrate the data from the legacy Documentum system to One Vault Quality Docs by developing the integrations which are currently available in the Documentum system
  • Below are the integrations developed and deployed as part of the integration effort
  • Abbvie QuickSign to OneVault: There is a retention period of 30 days for the agreements signed in QuickSign and client want to store these documents on regular basis into One Vault – Quality Docs system
  • Controlled Printing: Designed and Developed a Java application which allows to select a document for printing and send it directly to the printer
  • URL Redirect: Developed a custom program to redirect the legacy application URLs into legitimate Veeva documents link
  • Downstream apps Integration support: Assisting the down stream application teams with the REST APIs, VQL optimization, clarification on technical queries and assisting in the design activities
  • Responsibilities:
  • Requirements Discussion, clarification and bridge gaps between the development and business stakeholders
  • Provide estimates and Manage project delivery to meet the schedule and Quality
  • Manage the offshore technical team and guide them with all functional, technical and process oriented queries
  • Provide technical Veeva expertise for Quality Vault
  • Mentor the resources with necessary acquaintance for handling development and support of
  • Veeva project activities
  • Implement POCs for the new features like SDE job and configuring S3 bucket to write the exports
  • Design, Develop, Delivery and manage the integrations built using Veeva
  • Create the design documents, Functional Test scripts, VSIQs and PSIQs
  • Review and approve the documentation associated with Change Controls, impact assessment, traceability matrix, risk assessment and OQ, PQ test scenarios
  • Provide the application demos and capture the feedback from key stakeholders on regular basis
  • Managing the RAID logs and update/ escalate the issues to leadership team
  • Organizing the meetings and sharing meeting minutes, actions and decisions
  • Preparing project status reports and reporting to technical and business stake holders
  • Enable the configurations related to security, add picklist values, running reports, perform the data load activities and configure the reports as per business needs
  • Deliverable review and signoff

Lead

Cognizant Technology Solutions, Allergan
08.2022 - 05.2023
  • Client Cabot
  • Tools/ Technology Veeva Regulatory One, Agile approach
  • Team Size 4 (Application Offshore), 1 (Onshore)
  • Role Application/Migration, Cabot is a leading global specialty chemicals and performance materials company headquartered in Boston
  • Cabot has embarked on Veeva Regulatory One SaaS solution for the product Level Compliance and Registration Processes by migrating data from RMFS, WERCS, WERCS OR, JDE systems and spread sheets into the Regulatory One
  • Responsibilities:
  • Leading data migration for a project in Veeva RegulatoryOne module
  • End to end ownership of Veeva Regulatory One data migration from other web applications, spread sheets and file shares
  • Working with business analyst and end users to scope the migration requirements and finalizing the approach
  • Execute the workshops and lead customer discussions for the implementation of Veeva RegulatoryOne and coordinate with Veeva vendor for the actions identified
  • Define the migration strategy and prepare the data enrichment templates, mapping rules to migrate the content into RegulatoryOne
  • Migrate the data from Bill of Materials (BOM) to Bill of Substance (BOS) breakup and linking the objects thus establishing the parent child relationship up to 4 levels
  • Represent the Veeva project Architecture in the review meetings and get approval by platform team
  • Develop and manage day to day engagement activities
  • Manage overall project schedule and liaise with offshore team and Cabot Business and IT stakeholders for any course corrections
  • Conduct the demos and review the migrated data by creating test scenarios
  • Design the integration solution to export the data on periodic basis and thus refresh the BI reports using Dell Boomi
  • Plan and implement change control requests
  • Deliverable review and signoff
  • Project, AMS
  • Client Allergan
  • Tools/ Technology Veeva Quality Docs, Veeva eTMF, Veeva RIM, EMC Documentum 6.5 SP2, FirstDoc 6.x/7.x, Documentum Compliance Manager (DCM), Data migration, Liquent Insight publisher, Axway, Publishing
  • Team Size 8 (Application Offshore), 3 (Onshore)

Role Technical Lead

Allergan
02.2017 - 08.2022
  • Plc (AbbVie) is an American, Irish-domiciled pharmaceutical company that acquires, develops, manufactures, and markets brand name drugs and medical devices in the areas of medical aesthetics, eye care, central nervous system
  • Responsibilities:
  • Gather the requirements from business, transform them into technical requirements and provide estimates to business to implement these solutions
  • Support and lead the team on all discretionary projects and maintenance releases and build a plan for consuming and implementing discretionary changes
  • Access provisioning to users in Veeva eTMF, trouble shoot integration issues related to site creations
  • Coordinate with OKTA team with any AD integration issues
  • Analyze and create the life cycles by configure steps in Veeva Quality Docs
  • End to End ownership of Veeva eTMF application
  • Create objects and configure the workflows as per the business process defined in Veeva Quality Docs
  • Applying the atomic security on Documents and objects to restrict access based on role and business unit
  • Create the configuration sheets, review it by business and load into Quality Docs system using Vault Loader tool
  • Providing functional support to the business, take initiative in assigning, assess and troubleshoot end user issues that turnaround times conform to service level agreements
  • Hands-on experience on Service-Now
  • Assist releases with impact assessment, testing, user training materials creation and communication to end users
  • Perform the data exports of various divestiture requests using the out of the Box export options in Veeva Vault
  • Trouble shoot, resolve and coordinate with integration issues related to upstream and downstream apps into Veeva
  • Develop weekly, Monthly and Quarterly status reports and drive the calls with client to provide updates about ongoing activities progress, issues discussion and approvals from business on new enhancements.

Operations Lead

Cognizant Technology Solutions, Title EDM COE, Amgen Inc
04.2015 - 11.2016
  • Tools/ Technology EMC Documentum 6.5 SP2& 7.0, FirstDoc 6.x/7.x, EMC xPlore servers, ADTS 6.5/6.7 SP2, Linux, Veeva eTMF, Veeva Vault
  • Team Size 34 (Application Offshore), 6 (Onshore)
  • Role

Onite Project Lead

Amgen, Pfizer Pharmaceuticals
07.2013 - 04.2015
  • Is world’s largest independent biotechnology firm
  • It has several Enterprise Document Management systems in place for managing Trial Master Files, GxP, Adverse Event capture and Quality
  • Manage the ECM project team to deliver major application releases
  • Provide development, configuration, enhancement, system analysis, and maintenance support for EDM applications (EDM R&D/EPIC, EDM Quality, EDM Teams, etc…)
  • Responsible in interacting with clients for business functional requirements, technical requirements, and design specification for any major and minor release
  • Provide peer review to developers to ensure coding standards are followed consistent to Amgen’s compliance policy
  • Provide backline support for production issues that cannot resolved by 1st and 2nd tier support
  • Provide technical Documentum expertise to other EDM verticals such as EDM Quality, EPIC, EDM Corporate, EDM CRF, EDM Teams, etc…
  • Develop validation documents such as Installation/Operational Qualification (IQ/OQ), Requirement Specification, and System Design as part of project deliverables
  • These systems are gold tier applications with expected up-time of 99.5% and are supported by a team of 35 people in a 24 X 7 model
  • Additionally, to support, the team also works on Maintenance Releases and discretionary projects
  • The program was running into a lot of issues w.r.t problem records delays, non-standardized reporting and
  • Develop cost estimates and resource plans for enhancements, project upgrades and migration activities
  • Lead the team on all discretionary projects and maintenance releases and build a plan for consuming and implementing discretionary changes
  • Gather the requirements from business, transform them into technical requirements and provide estimates to business to implement these solutions
  • Streamline the process for recording, prioritizing, categorizing and closing the incidents
  • Ensuring the problem records management and RCA is performed as per ITIL requirements
  • Ensuring proper delivery of all enhancement and transition of knowledge from Project Team to the RUN team
  • Develop weekly operations report and drive the calls with client to provide update on ongoing activities progress, issues discussion and get approvals from business on key decisions
  • Prepare monthly deck on EDM COE to present to the Amgen higher management
  • Status reporting of different activities to the management and Business Reps
  • Drive change management process from initial change log to final closure in terms of getting approvals from business, integrated systems owners and Quality
  • Responsible to present the change in CAB meetings and LMR meetings
  • Interface with other enterprise groups (such as Infrastructure, J2EE, DBA, Storage, etc…) for application outages/ degradations and feasibility study/analysis to improve existing systems
  • Handling data export (Migration) requests from legal team and ensure to deliver the content within the timelines using Buldozer and TRUMigrate
  • Drive and assist with the annual DR exercises to comply with the company policies
  • Title PGS (Pfizer Global Supply)
  • Client, Tools EMC Documentum – Documentum Compliance Manager 6.5 SP2, Webtop 6.5 SP3, ADTS, xPlore Search, oracle 10g/11.x, KODAK Design to Launch (D2L)
  • Team Size 14 (Application Offshore), 3 (Onshore)

Infra Lead

Pfizer
01.2012 - 06.2013
  • Is one of the world’s Premier Biopharmaceutical company had several Enterprise Document Management systems in place for managing GxP, Adverse Event capture, R&D and Quality & Packaging Supply
  • Accenture is engaged to assist with implementation of enhancements/ Bug fixes and provide end to end support within the Manufacturing division of Pfizer
  • Responsibilities:
  • Discuss with business, Pfizer SMEs and Compliance team on new functional requirements/Bugs
  • Analyze and transform them to technical requirements
  • Provide the cost estimates and resource planning
  • Signoff the RSV define the plan for release and guide offshore team for implementation
  • Work on Build, deployments and update the design documentation
  • Resolve L3, Critical issues and drive the outage calls
  • Provided fixes to 70 critical bugs in ePALMS applications by adopting the technology
  • Weekly status reporting on Application Support and enhancements
  • Provide proposals to business on system tuning activities and additional enhancements which created business addition
  • Mentored 5 resources to feel comfortable with the domain knowledge and D2l product which helped in smooth delivery at unexpected vacations by resources
  • Project #7:
  • Title Merck Content and Collaboration Management (MCCM)
  • Client Merck Pharmaceuticals
  • Tools EMC Documentum, CSC FirstDoc, Webtop 5.x, ADTS, DTS, xPlore Search, GxPharma, Documentum Desktop
  • Team Size 18 (Application Offshore), 4 (Onshore)
  • Role Application/

Role Project Lead

Location Blue Bell
11.2009 - 12.2011
  • Merck is largest pharmaceutical company
  • MCCM is an ECM pool handling 20+ critical documentum applications serving the needs of GxP, clinical trials and R&D
  • Accenture is responsible to provide infra and application support 24X7 which covers upgrading patches on windows, Linux/ Unix servers on monthly/ quarterly basis, infrastructure and application maintenance
  • It also includes coordination with vendor for any bug fixes, working on new enhancements
  • Responsibilities:
  • Responsible to maintain the 20 + repositories hosted by the Merck applications
  • Performing Impact analysis for the system upgrades, patches on various environments and coordinating with other infra teams for smooth upgrades
  • Restart the application environments for the outages
  • Discuss with business and define the down time as per the process
  • Restart environments and mentoring junior resources to handle various activities like application restarts, guidance on application functionality
  • Ensuring the problem records management and RCA is performed as per ITIL requirements
  • Status reporting of different activities to the management and Business Reps
  • Working with Change Manager for transforming potential fixes to Change requests in Documentum
  • Providing trend analysis and issues escalation to higher level management via Metrics
  • Working on complex technical issues and conducting Knowledge Transfer Sessions to offshore teams
  • Support for the L3 level issues of submission management systems and drive the calls with business & IT stake holders
  • Project #8:
  • Title Hi-Life DMS
  • Client Henkel
  • Tools IBM DB2 Content Manager, IBM DB2 Document Manager, CSSAP, VB.NET, J2EE
  • Team Size 4 (Application Development) + 13 over all, Henkel is a world’s largest Consumer Goods firm
  • It had a Document Management System (DMS) to maintain their products as per the business standards
  • Accenture is responsible to set up DMS across various business units in High availability mode and mainta
  • Responsibilities:
  • Discuss with various stack holders on business requirements
  • Work on RFPs and discuss with account managers to sign off the contract
  • Work and manage Installation of IBM DB2 Content Manager product and implement the solution until the delivery
  • Guide team on technical issues and support business for testing
  • Working on project closure signoffs and transitioning to support team
  • 9:
  • Title MDocs (Marsh Document System)
  • Client Marsh
  • Tools EMC Documentum, Documentum Client for Outlook
  • Team Size 2

Role Consultant

08.2009 - 10.2009
  • Marsh is a leader in insurance Broking and risk management
  • The goal is to design a common DMS solution which can be deployed and configured for any Marsh business unit within any country
  • MDocs is the name of the Marsh project which will deliver this solution
  • Responsibilities
  • Analyze the business requirements and convert to technical requirements
  • Design and involve in architecture discussions as per Marsh needs to define ACL, Life Cycle, Workflow, taxonomy
  • Provide a solution Blueprint documentation
  • Project #9:
  • Title Global Document Management System (GDMS)
  • Client Wyeth Pharmaceuticals
  • Tools EMC Documentum, DCM, Webtop
  • Team Size 8

Role Senior Developer

AstraZeneca
08.2007 - 08.2009
  • Wyeth is a Pharma company which was now merged with Pfizer
  • It had 2 key applications GDMS and WCH-EDMS in R&D and Consumer Health Care domain respectively
  • GDMS is an application based on Documentum Content Server 5.3 SP2 and Documentum Compliance Manager (DCM)
  • The DCM product provides controlled document capabilities to support secure workflow, including electronic signatures for approval
  • Custom components have been developed to provide additional functionality to support key business processes such as document issuing and regulatory publishing
  • EDMS is a solution for multiple document content study reports, clinical protocols, submission documentation, test standards, manufacturing directions, labeling documentation, and master batch records
  • WCH-EDMS (Wyeth Consumer Healthcare Electronic Document Management System) was implemented in 1997 to support Scientific Affairs document processes related to Regulatory and Pharmaceutical Research & Development (PR&D) activities
  • Responsibilities
  • Analysis and creation of preliminary detailed design documents
  • Providing estimates for implementation
  • Configuration, coding and testing
  • Preparation of IQ, Build files to perform the deployments in test, QA and production environments
  • Updating System Design Specification (SDS)
  • Weekly Status reporting to Wyeth Management
  • Project #10, Tools EMC Documentum, Webtop 5.3 Sp2
  • Team Size 1

Role Senior Developer

AstraZeneca
03.2007 - 08.2007
  • Is large pharmaceutical company
  • EDossier is a professional information request (PIR) received from medical organizations
  • Once eDossier request is received from organizations, medical sales representatives forward that to the client's Troy application
  • There are 4 phases of process namely i) Request of eDossier, ii) Generation of eDossier, iii) Review of eDossier and iv) Fulfillment of eDossier
  • Responsibilities
  • Installation of Documentum products
  • Participation in requirements gathering and requirements analysis
  • Creation of requirements documents, technical design document and peer review
  • Creation of new DocApps and defining Object models using DAB
  • Customization of Webtop, Creating register tables
  • Preparation and review of unit test cases
  • Conducted technical and functional knowledge transfer sessions to team
  • Report status to onsite solutions manager
  • Discuss technical issues, including enhancements feasibility, estimates for changes with onsite solutions manager
  • Project #11:
  • Title ASSIMS (Asset Inventory Management System)
  • Client Accenture Internal
  • Tools EMC Documentum
  • Team Size 2

Role Developer

Location
08.2006 - 04.2007
  • Asset Inventory Management System is an application for storing, managing and sharing the assets created by the Portal and Content Management (PCM) capability
  • This is web based application which acts as a centralized repository system for PCM capability to store all assets like content management software like Documentum, Vignette, Bea weblogic portal, training materials ,training calendar, current resources list, client visit details, PCM town hall events
  • Responsibilities
  • Gathering requirements and Design
  • Development of application ASSIMS (Asset Inventory and Management System) independently
  • Installation of Content Server, configuring docbase, installation of Webtop, WDK
  • Coding and Deployment of application
  • Creation of Groups, permissions (ACLs) and providing access
  • Running of Documentum jobs for taking the latest logs on users operations on this application
  • 12:
  • Title SAS (Sales And Service)

Role Developer

Auto Club Group, ACG
04.2005 - 10.2006
  • XSLT-FO
  • Team Size 11, The ACG is a USA based property & casualty insurance company with its major business in the Michigan state
  • The main objective of the project is towards improving the business effectiveness through better underwriting and claim systems
  • I was involved in the development of i) quote and policies creation, ii) integration with third party tools for quote and policies creation and iii) modifications to policy
  • Key Responsibilities
  • Design and Implementation
  • Refining the requirements and discussions with client functionality team
  • Coding as per standards
  • Writing test scripts, testing the functionality
  • Interacting with client for functionality clarification and reporting status
  • Project #13:
  • Title PCM (Portal and Content Management)
  • Client Accenture
  • Tools EMC Documentum 5.3
  • Team Size 4

Role Developer

01.2005 - 03.2005
  • Portal and Content Management (PCM) center of excellence in IDC which is working on Assets creation, Development of POCs (Proof of Concepts) and trainings in Documentum
  • Key Responsibilities
  • Developing Proof of concepts in Documentum
  • Gaining expertise in Documentum products
  • Acquiring skills in other Content Management tool Vignette through internal training conducted by PCM Capability
  • Preparation of reports on comparison between different Content Management tools
  • Conducting knowledge transfer sessions to new joiners
  • Project #14:
  • Title TALON2.NET
  • Project Type Testing
  • Client Harley Davidson
  • Tools .NET
  • Team Size 17

Role Tester

Location
09.2004 - 12.2004
  • Harley Davidson is a well-known motor bikes company in USA
  • Talon.NET project creates a software package functionally to client which mainly deals with the activities of the dealer like Admin, Inventory, Point of Sale, Services and Vehicle Sales
  • Key Responsibilities
  • Testing of all Modules
  • Helping new resources in understanding the functionality

Education

Master of Science - Computer Applications Development

Achaya Nagarjuna University
07-2003

Skills

  • Operations management
  • Human resources management
  • Effective communication
  • Excellent oral and written communication
  • Relationship building and management
  • Client service
  • Onboarding and training
  • Strategic planning
  • Project management
  • Budgeting and forecasting
  • Presentation skills
  • Data analytics
  • Professional rapport

Certification

  • Project Management Professional (PMP) - Project Management Institute.

Timeline

Business Operator

Amgen
04.2024 - Current

Developer, Specialist

Cognizant Technology Solutions, Amgen
04.2024 - Current

Technical Lead

Cognizant Technology Solutions, Veeva
05.2023 - 03.2024

Lead

Cognizant Technology Solutions, Allergan
08.2022 - 05.2023

Role Technical Lead

Allergan
02.2017 - 08.2022

Operations Lead

Cognizant Technology Solutions, Title EDM COE, Amgen Inc
04.2015 - 11.2016

Onite Project Lead

Amgen, Pfizer Pharmaceuticals
07.2013 - 04.2015

Infra Lead

Pfizer
01.2012 - 06.2013

Role Project Lead

Location Blue Bell
11.2009 - 12.2011

Role Consultant

08.2009 - 10.2009

Role Senior Developer

AstraZeneca
08.2007 - 08.2009

Role Senior Developer

AstraZeneca
03.2007 - 08.2007

Role Developer

Location
08.2006 - 04.2007

Role Developer

Auto Club Group, ACG
04.2005 - 10.2006

Role Developer

01.2005 - 03.2005

Role Tester

Location
09.2004 - 12.2004

Master of Science - Computer Applications Development

Achaya Nagarjuna University

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