Jesse Reyes Financial Services Professional Email & Phone Number

Port Hueneme, CA, US

Long Beach, California, US

Prepare detailed documentation for submission to Government Agencies.Provide data entry and inventory management.Coordinate Plan Submissions to State Agencies: Lead the gathering, preparation and packaging of documents for purposes of completing a required submission to a state agency or regulator. This responsibility entails setting up a project plan for.

US

Review all financials including total maintenance/operational expenses and evaluate reserves and all income to ensure we are meeting and exceeding our budgets goals for Surfside III HOA. Participate and give feedback on spending cuts and spending increases to help balance the COA budget.

Educating and providing clients with a variety of financials services including life insurance, annuities, disability insurance, estate planning, property and casualty insurance, health insurance and much more. My goal is to help clients save money and make money and follow the company mission of no family left behind. My focus is middle class Americans.

Thousand Oaks, CA, US

• Spearhead data verification activities diligently to ensure swift and accurate responses to health authorities when requests for information are received.
• Ensure timely and appropriate workflows and procedures regarding document tracking, indexing, retrieving, and disseminating of regulatory agency submissions as defined by Regulatory Operation management.
• Ensure that regulatory documents comply with the relevant guidelines for content and format and that the content of the document is accurate and reflects the information / data in the source documentation.
• Aid in the creation of technical documents by providing templates for the similarity section of CTA’s and MA’s and preparing and filing NDA and BLA applications. Additionally, assist in the authoring of internal.
• Enforce quality control measures effectively for the review and finalization of documents.
• Actively collaborate with multidisciplinary teams to refine document processes and guarantee the accuracy, adequacy, and consistency of documents.

Franklin Lakes, New Jersey, US

• I ran the US region marketing MMS business unit with over 25 marketing managers to ensure timely submission of ad/promotional documents in Veeva PromoMats.
• Coordinate with the marketing team to handle documents, ensuring compliance with FDA regulations in Veeva Promo Mats workflow for MLR review/approval. Also, upload supporting reference documents.
• Routing ad/promotional material and internal training material for review/approval in Veeva Promo Mats.
• Create claim review records for medical, legal, and regulatory review. Generate Veeva reports for all document submissions and send reports to the Director of Operations and consolidating claim matrix spreadsheets for.
• Thoroughly review and proofread content, annotating and anchoring reference links to validate claims in documents. Edit using Adobe Creative Cloud Suite before uploading to Veeva.
• Keep the marketing team informed about document status in Veeva. Take necessary actions until documents are fully approved for distribution.

Franklin Lakes, New Jersey, US

Supporting the Marketing Communications Team @ BD with document workflow in Veeva PromoMats and routing the documents to medical, legal and regulatory reviewers and approvers. Additionally support the customer relationship management database (Salesforce). Other projects as assigned.

Thousand Oaks, CA, US

• Independently edited, proofread, formatted, and/or wrote SOPs or Work Instructions based on process maps or discussions with Subject Matter Experts (SMEs) and Process Leads.
• Provided Quality Assurance standards by quality checking/revising existing documentation according to SOPs and Guidance documents.
• Served as a "scribe" during meetings with subject matter experts, writing documents according to templates/style guides.
• Led a team of subject matter experts to facilitate discussions and reviews of processes and documentation. Depending on experience, may have acted as a project manager for sub-projects representing R&D Quality processes.
• Acted as a liaison between Quality group members (e.g., Business Process Modelers) and the business (e.g., Business Process Owner, Document Owner, Authors, Subject Matter Experts).
• Managed documents through the established R&D Document Review process using the electronic document repository (Veeva-CDOCs) and eCTD for regulatory submissions.

Waltham, MA, US

• Oversaw documents including redline documents and document change orders.
• Collaborate with product development teams to process document change orders at Thermo Fisher Scientific.
• Handle document change orders for GTS/Clinical Program Management.
• Manage design history files in Agile PLM.
• Update document trackers using SharePoint.
• Send weekly reminders for document review and approval via Agile PLM workflow.

Thousand Oaks, CA, US

• Assist Research and Development with implementing electronic document management strategy and transitioning to RIM.
• Experienced in Regulatory Submissions (IND, NDA, CTA, JNDA) for Nonclinical and/or Clinical Modules across multiple countries.
• Manage regulated electronic documents from creation to archival following procedures and guidance documents.
• Daily tasks: create drafts, check document quality/formatting, proofread, route for review/approval, and provide system support to users.
• Manage document templates, create electronic metadata records, and clean up legacy documents.
• Provide project management support for various activities and limited projects.

Santa Monica, California, US

• My function was steward documents through Veeva Vault including change requests for CMC protocol documents and converting them to executed protocol documents.
• Diligently support the CMC site by preparing, circulating, and handling all standard operating procedures (SOPs) and associated forms, along with other necessary documents as needed.
• Establish and consistently maintain a Deviation, CAPA, EV, and Change Control Management System in compliance with regulatory, quality, and company requirements using GXP systems.
• Expertly provide guidance and advice on methods, procedures, standardization, and requirements associated with this system, including computer system validation.
• Thoroughly establish the process and procedures for identifying, collecting, distributing, and filing controlled documents for the site. This includes writing and maintaining document control procedures and actively.
• Efficiently manage the lifecycle of SOPs and other document types utilizing a Controlled Document Management System.

San Francisco, CA, US

Personal shopper for customers delivering groceries at requested time and location.

Minneapolis, MN, US

Analyzes proposed changes of product design to determine effect on overall product and system @ Medtronic. Coordinates modification records for management control. Establishes change orders and prepares for change authorization and documentation by company and subcontractor. Prepares reports of change effect on overall product. Reviews and analyzes.

Thousand Oaks, CA, US

Management of process documentation per required process (e.g. Standard Operating Procedure [SOP] on SOPs) in accordance with agreed timelines and in adherence with format, content and style guidelines, giving consideration to usability and ensuring accuracy, consistency and quality @ Amgen. Development and facilitation of the creation and/or revision of.

Thousand Oaks, CA, US

Building strong relationships by training agency/supplier partners to efficiently and effectively submit digital assets for archive into Zinc @ AmgenEnsuring a regulatory release date of digital projects before archivingWorking with IS team to develop SOW for the implementation of new DAM system Created workflow for the archive process for implementation.

Thousand Oaks, CA, US

Processing (formatting) Standard Operating Procedures (SOP's) and other vital documents to ensure that the documents follow company policy and guidelines for Amgen. Scanning documents into company scanning software for retrieval and or archival at a later time. Indexing and importing documents into the company software for easy access and retrieval..

Master Of Business Administration (M.B.A.)

Liberal Arts

Bachelor Of Science (B.S.), Business Administration And Management, General

Master Of Business Administration - Mba, Business Administration And Management, General