ตัวอย่าง Resume นักวิเคราะห์ธุรกิจ (Business Analyst) ฉบับที่ 174
Resume Example Business Analyst #0174 ประมาณ 2453 คำ
เรซูเม่ฉบับนี้เป็นตัวอย่างสำหรับตำแหน่ง Business Analyst ระดับมืออาชีพ มีประสบการณ์รวมประมาณ 5 ปี เรานำมาวิเคราะห์เพื่อให้เห็นว่า โครงสร้างมีจุดเด่นอย่างไร และส่วนใดนำไปปรับใช้กับข้อมูลของคุณได้
จุดเด่นของฉบับนี้ แสดงประสบการณ์ทำงาน 9 ตำแหน่ง พร้อมหน้าที่และผลงานของแต่ละช่วงอย่างเป็นลำดับ
สิ่งที่ควรสังเกตในตัวอย่างนี้
- ประวัติงานต่อเนื่อง 5 ปี เห็นการเติบโตของตำแหน่งได้ชัด
- มีการกล่าวถึง Salesforce ซึ่งเป็นสิ่งที่ HR สายนักวิเคราะห์ธุรกิจ ให้ความสำคัญ
- ประสบการณ์ 9 ตำแหน่ง ไล่ระดับจาก Junior ขึ้นไปจนถึงตำแหน่งปัจจุบัน
- Professional Summary กระชับ ใช้คำที่สื่อความสามารถได้จริง
- มีทักษะแยกเป็นหมวด 39+ รายการ ให้ HR เห็นสเปกครบถ้วน
Professional Summary
Highly motivated Sales Associate with extensive customer service and sales experience. Outgoing sales professional with track record of driving increased sales, improving buying experience and elevating company profile with target market. Business Analysis
Experience
Business Analyst08/2021 - Current
LIMS, HP-QC, Track Wise Testing Tools Ambit Group
- Managed projects and served as primary liaison between client and multiple internal groups to clarify goals and meet standards and deadlines.
- Defined key data points and data sources to track against measurable performance indicators and produce useful reports. Involved in conducting Functionality testing. Integration testing, Regression testing and User.
- Responsible for gathering and analyzing Business and system functional requirements and for understanding and translating these needs into Business Requirement Specification (BRS), System Requirement Specification (SRS) documents, Client requirements document (CRD), and Functional specification document (FSD).
- Experience with AGILE Tool and methodology. Responsible for the full HIPAA compliance lifecycle from gap analysis, mapping, implementation and testing for Medicaid Claims.
- Studied business requirements and technical specifications to create test documentation in Agile
- Analyzed Business Requirements and segregated them into high level and low-level Use Cases, Activity Diagrams / State Chart Diagrams using Rational Rose according to UML methodology thus defining the Data Process Models.
- Conducted user interviews, gathered requirements, analyzed the requirements using Rational Rose requisite pro - RUP
- Designed and developed Use Cases, Activity Diagrams, Sequence Diagrams, OOD (Object oriented Design)
- Evaluated Business Requirements (BRS) for enterprise business applications integration and reviewed existing documentation for current systems to create AS-IS and TO-BE processes for GAP analysis.
Business Analyst / Responsibility03/2020 - Current
Ambit Group
- Understanding and analyzing Business requirements and design specification and determine the scope of testing.
- Steered requirements meetings during business requirements gathering sessions across multiple stakeholder groups (product owner, SMEs, and process owners).
- Created various documents like the Software Requirement Specifications (SRS), Business requirements document (BRD), Use Case Specifications, Functional Specifications (FSD), Systems Design Specification (SDS)
- Resolved the data mapping issues by working with the business stakeholders and development team.
- Performed "AS-IS" and "TO-BE" business process flow for clear translation of Functional to system requirement specification.
- Led multiple Agile teams on SAFe methodologies with knowledge of embedded SDLC process.
- Implemented Agile Scrum methodology guidelines to build artifacts in different sprints and phases of the application development process.
- Performed GAP analysis for data from various source systems & documenting Business, Functional and Non-Functional Requirements into Business Requirement Documents (BRDS) and Business System Document (BSDs).
- Maintained data mapping and data transformation documentation.
- Planned and defined system requirements to Wire Frame with Use Case, Use Case Scenario and Use Case Narrative using the UML (Unified Modeling Language) methodologies.
- Worked with MS Visio to create workflow models and process flow models after reviewing URS and FRS.
- Liaison between Clinical staff, Claims Operations, IT developers, Project Managers and stakeholders providing coordination, support and facilitating projects
- Collected data from patient examinations; prepare medical records for sponsor's clinical report forms.
- Involved in preparing documentation of the computer system validation lifecycle, in accordance with FDA regulations (21 CFR 11, 820,210 & 211).
- Coordinated product complaints through Trackwise. Initiated investigation and identification of root cause for defects returned from the field under FDA and GMP guidelines using CAPA Trackwise.
- Reviewed and updated IQ/OQ/PQ Summary Reports, Validation Final Reports and Go Live memos.
- Developed Validation Test Plan in conjunction with FDA regulations.
- Was responsible for reviewing Installation Qualification (IQ)/Operational Qualification (OQ)/Performance Qualification (PQ) test scripts.
- Developed test cases/scripts (IQ, OQ) for verification against specifications to ensure fitness for intended use of the Spread sheets.
- Helped with Data Mapping between the data mart and the Source Systems.
- Utilized defect tracking tool JIRA for reporting bugs/defects in functionality. Conducted weekly status meeting with development teams for defect resolution. Utilized SQL for querying database tables during testing.
- Used HP ALM for Bug tracking and involved in developing and implementing the test strategy.
- Actively involved in analyzing the business requirements to develop test plans, test cases and test scripts.
- Supported the testing team with Defect Management, Requirement Analysis and SQL development for back-end and regression testing and maintained the HP Quality Center with the latest updates on the defects.
- Involved in conducting Functionality testing, Integration testing. Regression testing and User.
- Coordinated with development team for all the issues related to deployment and defect tracking in HP Quality Center.
Business Analyst / Responsibility01/2017 - 03/2020
Ambit Group
- Gathered business Re-designed and Implemented defect management processes, Created Defect Matrices, generating defect reports on weekly basis requirements by driving user-group meetings and working with various global, cross-functional and virtual teams
- Gathered and document Business Requirements document (BRD), Functional and Non-Functional Requirements (FRD)
- Followed and applied Agile (Scrum) methodology in defining problem, gathering requirements, business
- modeling and communicating with the technical team for development of the system.
- Used PTC Windchill RV&S (former Integrity, as an Application Lifecycle Management [ALM] system) to track development progress, tasks, issues, user stories, sprints, etc.
- Worked in different types of Projects such as CTMS Clinical Trial Management System and CDC Clinical Document Control - Data Analysis for yearly forecasting, LMS usage and other reporting needs
- Work collaboratively with business owners to identify areas where improvements are needed and to develop and monitor appropriate action plans to ensure a consistent focus on priority issues. General knowledge of key performance indicators (KPIs) and metrics
- Develop a strategy to design SQL queries using the Clinical Data Warehouse (Confidential) query tool
- Assess and analyzed database query reports to search for potential research candidates in Confidential Clinical Data Warehouse
- Administered Salesforce CRM applications for Sales, Marketing and Support Departments.
- Involved in designing business requirement collection approach based on the Agile SCRUM SDLC Methodology
- Access to Windchill and was responsible to route documentation by creating ECR(Enterprise Change Request), CO(Change orders) & CA(Change Activity).
- Extensive Training Experience Content Management SharePoint CTMS Power User Manager/Supervisor of Staff
- Participated in business process modeling sessions with Business Owners, SMEs, Product Manager to carve out the As-Is and To-Be process flow.
- Involved in writing Use Cases and Functional Requirement Documents as well as for creating Use Case diagrams, Activity diagrams, State diagrams based on UML Methodology and business object modeling flow diagrams using MS Visio/Rational Rose.
- Performed data analysis for the existing data warehouse and changed the internal schema for performance
- Understands systems integration and applications in the Avaya environment
- Prepared Business Process Models that includes modeling of all the activities of the business from the conceptual to procedural level. Followed top down, leveled technique for building Business Process Models
- Analyzed the sources and targets, transforming the data, mapping the data and populating the data into targets by using Workflow Manager, and Workflow Monitor
- Conducted GAP Analysis in order to be in compliance with 21 CFR Part 11.
- Initiated investigation and identification of root cause for defects returned from the field under FDA and GMP guidelines using CAPA
Trackwise.
- Analyzed software's to ensure compliance with 21 CFR PART 11 respect to Audit Trails, Data Integrity and Data Security of the application.
- Prepared documentation for all the aspects of Validation in accordance with 21 CFR Part 11 regulations.
- Managed the overall execution of IQ/OQ/PQ, including resource management, scheduling, Incident management and status reporting.
- Involved in creating test bed to check the Installation and Operational Qualification (IQ/OQ) for the application.
- Reviewed Validation Deliverables from the QA perspective, using pharmaceutical GxP practices and imported scanned all the documents in Documentum d2 for QA manager approval.
- Involved in preparation and documentation for all aspects of the computer system validation to ensure compliance in accordance with cGXP (cGMP, cGLP and CGCP) and FDA rules and regulations.
- Performed Validation Activities as per GAMP 5, CSV, Annex 11, FDA 21 CFR Part 11, FDA 21 CFR Part 820 and GXP (GCP/GMP/GLP) standards strategy, procedures, and techniques
- Prepared a Data Migration Summary Report stating the data migration activities taken place while loading the static data in the LIMS application.
- Tested system against the FDA, GXP Compliance Risk, 21 CFR regulations 210, 211
- Involved in defining the source to target data mappings, business rules, and data definitions.
- Performed Data mapping, logical data modeling, created class diagrams and ER diagrams and used SQL queries to filter data
- Provide Avaya systems programming services as needed
- Performed complex detail/summary filtering, SQL querying and Adhoc analysis
- Utilized defect tracking tool JIRA for reporting bugs/defects in functionality. Conducted weekly status meeting with development teams for defect resolution. Utilized SQL for querying database tables during testing.
- Reviewed test cases for QA and provided assistance while testing. And performed User Acceptance Testing to improve the User Experience of the application.
- Assisted development team with designing the application to meet end user business needs.
- Worked with the UAT and QA teams to conduct an assessment and determine how effective UAT and QA guidelines can help the company achieve timely completion of projects
Business Analyst / Responsibility05/2013-01/2017
American Heart Association
- Gathered business Re-designed and Implemented defect management processes, Created Defect Matrices, generating defect reports on
- weekly basis requirements by driving user-group meetings and working with various global, cross-functional and virtual teams
- Gathered and document Business Requirements document (BRD), Functional and Non- Functional Requirements (FRD)
- Followed and applied Agile (Scrum) methodology in defining problem, gathering requirements, business
- modeling and communicating with the technical team for development of the system.
- Used PTC Windchill RV&S (former Integrity, as an Application Lifecycle Management [ALM] system) to track development progress, tasks, issues, user stories, sprints, etc.
- Worked in different types of Projects such as CTMS Clinical Trial Management System and CDC Clinical Document Control
- Data Analysis for yearly forecasting, LMS usage and other reporting needs
- Work collaboratively with business owners to identify areas where improvements are needed and to develop and monitor appropriate action
- plans to ensure a consistent focus on priority issues. General knowledge of key performance indicators (KPIs) and metrics
- Develop a strategy to design SQL queries using the Clinical Data Warehouse (Confidential) query tool
- Assess and analyzed database query reports to search for potential research candidates in Confidential Clinical Data Warehouse
- Administered Salesforce CRM applications for Sales, Marketing and Support Departments.
- Involved in designing business requirement collection approach based on the Agile SCRUM SDLC Methodology
- Access to Windchill and was responsible to route documentation by creating ECR(Enterprise Change Request), CO(Change orders) &
CA(Change Activity).
- Extensive Training Experience Content Management SharePoint CTMS Power User Manager/Supervisor of Staff
- Participated in business process modeling sessions with Business Owners, SMEs, Product Manager to carve out the As-Is and To-Be process flow.
- Involved in writing Use Cases and Functional Requirement Documents as well as for creating Use Case diagrams, Activity diagrams, State diagrams based on UML Methodology and business object modeling flow diagrams using MS Visio/Rational Rose.
- Performed data analysis for the existing data warehouse and changed the internal schema for performance
- Understands systems integration and applications in the Avaya environment
- Prepared Business Process Models that includes modeling of all the activities of the business from the conceptual to procedural level.
- Followed top down, leveled technique for building Business Process Models
- Analyzed the sources and targets, transforming the data, mapping the data and populating the data into targets by using Workflow Manager
and Workflow Monitor
- Conducted GAP Analysis in order to be in compliance with 21 CFR Part 11.
- Initiated investigation and identification of root cause for defects returned from the field under FDA and GMP guidelines using CAPA
Trackwise.
- Analyzed software's to ensure compliance with 21 CFR PART 11 respect to Audit Trails, Data Integrity and Data Security of the application.
- Prepared documentation for all the aspects of Validation in accordance with 21 CFR Part 11 regulations.
- Managed the overall execution of IQ/OQ/PQ, including resource management, scheduling, Incident management and status reporting.
- Involved in creating test bed to check the Installation and Operational Qualification (IQ/OQ) for the application.
- Reviewed Validation Deliverables from the QA perspective, using pharmaceutical GxP practices and imported scanned all the documents in Documentum d2 for QA manager approval.
- Involved in preparation and documentation for all aspects of the computer system validation to ensure compliance in accordance with cGXP (cGMP, cGLP and CGCP) and FDA rules and regulations.
- Performed Validation Activities as per GAMP 5, CSV, Annex 11, FDA 21 CFR Part 11, FDA 21 CFR Part 820 and GXP (GCP/GMP/GLP)
- standards strategy, procedures, and techniques
- Prepared a Data Migration Summary Report stating the data migration activities taken place while loading the static data in the LIMS application.
- Tested system against the FDA, GXP Compliance Risk, 21 CFR regulations 210, 211
- Involved in defining the source to target data mappings, business rules, and data definitions.
- Performed Data mapping, logical data modeling, created class diagrams and ER diagrams and used SQL queries to filter data
- Provide Avaya systems programming services as needed
- Performed complex detail/summary filtering, SQL querying and Adhoc analysis
- Utilized defect tracking tool JIRA for reporting bugs/defects in functionality. Conducted weekly status meeting with development teams for defect resolution. Utilized SQL for querying database tables during testing.
- Reviewed test cases for QA and provided assistance while testing. And performed User Acceptance Testing to improve the User Experience of the application.
- Assisted development team with designing the application to meet end user business needs.
- Worked with the UAT and QA teams to conduct an assessment and determine how effective UAT and QA guidelines can help the company
- achieve timely completion of projects
- Associate in Education: Science Education, 05/2019
Position
Virginia Commonwealth University
- Associate of Science: Biology, 06/2013 Nova Community College - Annandale, VA
Skills
IQ/OQ/PQLIMSAudit trailsTest PlanURSFRSSOP'sCAPAValidation planRTMRequirement Analysisdetail designBusiness RulesData flow Diagramsdata definition tabledata modelingFDA Quality system regulationsSOXMaster ControlGXPs (GMPGLPGCP) MethodologiesAgileWaterfall ModelPrototypingKanbanScrumban SAFe Skills:HP ALM/Quality CenterTFSJIRA DatabaseMySQLOracleSQL ServerSQL Business ToolsVeeva CRMVeeva VaultSalesforce.comSiebelHP Quality Center.
สรุปว่าจะได้อะไรจากตัวอย่างนี้
ตัวอย่างนี้ช่วยให้เห็นแนวทางการเขียนเรซูเม่สำหรับตำแหน่ง Business Analyst ประสบการณ์ 5 ปี โดยเปิดด้วยบทสรุปที่บอกจุดเด่นของผู้สมัคร ตามด้วยประสบการณ์ทำงาน 9 ตำแหน่ง พร้อมทักษะที่เกี่ยวข้องกับงาน คุณสามารถนำลำดับและวิธีนำเสนอไปปรับใช้ โดยเปลี่ยนรายละเอียดให้ตรงกับประสบการณ์จริงของคุณ
อย่างไรก็ตาม เรซูเม่ที่ชนะต้องเขียนให้ตรงตำแหน่งที่คุณสมัครโดยเฉพาะ ตัวอย่างนี้คือต้นแบบ ไม่ใช่สำเนา ทีมเรซูเม่ของเรารับเขียน Resume และ Cover Letter ภาษาอังกฤษให้โดดเด่นจากคู่แข่ง ส่งงานใน 2 วัน รับประกันความพึงพอใจ