Brian Keel, Mba

Brian Keel, Mba Email and Phone Number

Flight Test Analyst at Axient Corporation @ Axient
Brian Keel, Mba's Location
New Market, Alabama, United States, United States
Brian Keel, Mba's Contact Details

Brian Keel, Mba work email

Brian Keel, Mba personal email

n/a

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About Brian Keel, Mba

Brian Keel, Mba is a Flight Test Analyst at Axient Corporation at Axient. He possess expertise in gmp, pharmaceutical industry, sop, fda, 21 cfr part 11 and 21 more skills. Colleagues describe him as "Brian is a good team player. Easy to get along with. "

Brian Keel, Mba's Current Company Details
Axient

Axient

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Flight Test Analyst at Axient Corporation
Brian Keel, Mba Work Experience Details
  • Axient
    Flight Test Analyst
    Axient Aug 2021 - Present
    Huntsville, Alabama, United States
    • Assists the Mission Director, Mission Manager, Integrated Event Test Team (IETT), and Element Mission Managers in planning, coordinating, integrating, and executing all BMDS Test Concept of Operations (CONOPs) phases of testing.• Supports GMD component integration activities for flight test events• Supports the development of test plans, scheduling, test objectives, test execution documentation, procedures, requirements, infrastructure, and the development, coordination, integration, and conduct of test and evaluation events• Serves as the GM Contract Support Specialist (CSS) Lead for various flight tests.• Serves as the Task Management Point of Contact to review, collaborate, comment, and complete tasks assigned to the GMT organization.• Works closely with MDA, Navy, Army, Air Force, Space Force, and other DoD civilian and contract personnel across multiple levels to identify, manage, and verify dependencies between facility and system-level requirements to support deployment of BMDS flight test capabilities.• Gathers Objective Evidence from multiple sources to ensure that the Entrance Criteria, as defined by the GMD Test Plan, aligns with the needs of the GM Test Program and the BMDS CONOPS.• Supports technical reviews and cross-functional documentation reviews.• Reports to test management on progress and works with them to resolve any issues.
  • Millennium Engineering And Integration
    Flight Test Analyst, Missile Defense Agency
    Millennium Engineering And Integration Nov 2019 - Aug 2021
    Huntsville, Alabama, United States
    • Assisted the Mission Director, Mission Manager, Integrated Event Test Team (IETT), and Element Mission Managers in planning, coordinating, integrating, and executing all BMDS Test Concept of Operations (CONOPs) phases of testing.• Supported GMD component integration activities for flight test events• Supported the development of test plans, scheduling, test objectives, test execution documentation, procedures, requirements, infrastructure, and the development, coordination, integration, and conduct of test and evaluation events• Served as the GM Contract Support Specialist (CSS) Lead for various flight tests.• Served as the Task Management Point of Contact to review, collaborate, comment, and complete tasks assigned to the GMT organization.• Worked closely with MDA, Navy, Army, Air Force, Space Force, and other DoD civilian and contract personnel across multiple levels to identify, manage, and verify dependencies between facility and system-level requirements to support deployment of BMDS flight test capabilities.• Gathered Objective Evidence from multiple sources to ensure that the Entrance Criteria, as defined by the GMD Test Plan, aligns with the needs of the GM Test Program and the BMDS CONOPS.• Supported technical reviews and cross-functional documentation reviews.• Reported to test management on progress and worked with them to resolve any issues.
  • Millennium Engineering And Integration
    Mission Support & Integration Analyst, Missile Defense Agency
    Millennium Engineering And Integration Apr 2019 - Nov 2019
    Huntsville, Alabama Area
    • Prepared Program Requirements Documents (PRDs) and Operation Requirements Documents (ORs) for MDA/GM flight test missions in accordance with established Universal Documentation System (UDS) requirements.• Assisted in the development of test plans, test objectives, test execution documentation, procedures, requirements, infrastructure, and the development, coordination, integration, and conduct of test and evaluation events.• Coordinated with civilian federal employees, contractors, and support agencies to review, collaborate, and integrate support requirements for MDA/GM flight test missions.• Coordinated identified requirements with test ranges to include infrastructure, instrumentation, auxiliary sensors, and/or modifications to existing facilities.• Documented detailed requirements for test assets and instrumentation.• Supported GMD component integration for flight test activities.• Assisted in the management of the Flight Test Support calendar to capture the current operational tempo for daily Flight Test Support activities and to provide situational awareness to aid in efficient planning and meeting deconfliction.• Collaborated with federal civilian employees, contractors, and support agencies to establish, maintain, and distribute documentation status charts for upcoming flight test missions in support of on-time/on-readiness mission execution.
  • Par Pharmaceutical
    Manager, Dea Compliance - Distribution & Som
    Par Pharmaceutical Apr 2017 - Sep 2018
    Huntsville, Alabama
    • Responsible for overseeing the day-to-day operations of Par Pharmaceutical’s Distributor, Importer, and Exporter DEA registrations, including all responsibilities listed below under the DEA Compliance – Sr. DEA Compliance Specialist role.• Responsible for overseeing the day-to-day operations of Par Pharmaceutical’s Suspicious Order Monitoring (SOM) Program.• Responsible for directing and performing thorough investigations for orders of interest and ensuring timely completion of reviews and investigations.• Responsible for evaluating all new controlled substance customers and existing customers ordering controlled substances for the first time. This includes a detailed review of the registration as well as a site visit to the registered location to establish relationships and discuss our Suspicious Order Monitoring (SOM) programs and due diligence efforts.• Responsible for overseeing and managing the efforts of Suspicious Order Monitoring Analysts, providing guidance and performance feedback.• Responsible for managing and continually evaluating the company’s Suspicious Order Monitoring program and the established control limits.• Responsible for staying current on product and geographic abuse and diversion trends as well as industry trends, best practices, and DEA guidance.• Responsible for acting as a liaison, subject matter expert, and contact point for all things related to the company’s Distributor, Importer, and Exporter registrations as well as Suspicious Order Monitoring, including communication with each customer and account services executive as necessary.• Responsible for serving as the primary contact with the Drug Enforcement Administration and the Board of Pharmacy in the event of an audit.
  • Par Pharmaceutical
    Sr. Dea Compliance Specialist
    Par Pharmaceutical Feb 2016 - Apr 2017
    Huntsville, Alabama Area
    Responsible for:• ensuring compliance with the distribution reporting requirements of the DEA. This involves generating ARCOS reports for Distribution, inventory data to support the end of year or 1/31 letters or UN reporting, generating 106 forms for in-transit thefts/losses and participating in the review and/or reporting of suspicious orders.•reviewing state required distribution reports for accuracy and submit them to the appropriate State agency. I work with Distribution and IT to resolve any discrepancies. •Assisting with responding to subpoenas or other law enforcement inquiries for product or distribution reports. Informs management, Legal and Security of the request and the outcome.•Analyzing and spot checking Distribution cycle counts, end of year inventory and other accompanying data submitted to the DEA Compliance Group, to support the end of year report filing (1/31 letter). •Working closely with Distribution to gather data reflecting all shipments, receipts and destructions. Analyze the data for accuracy throughout the year and uses this information to generate ARCOS reports for periodic submission to DEA. •Interfacing with other departments such as Distribution, Customer Service, Sales, Security, Legal or IT to keep abreast of product, facility or process changes affecting the DEA compliance of our distribution facilities.•Completing DEA 106 theft/loss forms for in-transit theft/loss reporting to DEA. Partners with Security, Distribution and management as required to assist with investigative efforts and helps to monitor that any required corrective actions are implemented. •Completing DEA 222 order forms for signature by an authorized power of attorney, for the Distributor and Analytical DEA registrations. Record form information in the appropriate logbook for tracking purposes.•Interfacing with DEA as required on issues relating to reporting requirements and other miscellaneous requests.
  • Par Pharmaceutical
    Dea Compliance Specialist
    Par Pharmaceutical Oct 2015 - Feb 2016
    Huntsville, Alabama Area
    Responsible for:• ensuring compliance with the distribution reporting requirements of the DEA. This involves generating ARCOS reports for Distribution, inventory data to support the end of year or 1/31 letters or UN reporting, generating 106 forms for in-transit thefts/losses and participating in the review and/or reporting of suspicious orders.•reviewing state required distribution reports for accuracy and submit them to the appropriate State agency. I work with Distribution and IT to resolve any discrepancies. •Assisting with responding to subpoenas or other law enforcement inquiries for product or distribution reports. Informs management, Legal and Security of the request and the outcome.•Analyzing and spot checking Distribution cycle counts, end of year inventory and other accompanying data submitted to the DEA Compliance Group, to support the end of year report filing (1/31 letter). •Working closely with Distribution to gather data reflecting all shipments, receipts and destructions. Analyze the data for accuracy throughout the year and uses this information to generate ARCOS reports for periodic submission to DEA. •Interfacing with other departments such as Distribution, Customer Service, Sales, Security, Legal or IT to keep abreast of product, facility or process changes affecting the DEA compliance of our distribution facilities.•Completing DEA 106 theft/loss forms for in-transit theft/loss reporting to DEA. Partners with Security, Distribution and management as required to assist with investigative efforts and helps to monitor that any required corrective actions are implemented. •Completing DEA 222 order forms for signature by an authorized power of attorney, for the Distributor and Analytical DEA registrations. Record form information in the appropriate logbook for tracking purposes.•Interfacing with DEA as required on issues relating to reporting requirements and other miscellaneous requests.
  • Qualitest Pharmaceuticals
    Dea Compliance Specialist
    Qualitest Pharmaceuticals Jul 2013 - Oct 2015
    Huntsville, Alabama Area
    Responsible for:• ensuring compliance with the distribution reporting requirements of the DEA. This involves generating ARCOS reports for Distribution, inventory data to support the end of year or 1/31 letters or UN reporting, generating 106 forms for in-transit thefts/losses and participating in the review and/or reporting of suspicious orders.•reviewing state required distribution reports for accuracy and submit them to the appropriate State agency. I work with Distribution and IT to resolve any discrepancies. •Assisting with responding to subpoenas or other law enforcement inquiries for product or distribution reports. Informs management, Legal and Security of the request and the outcome.•Analyzing and spot checking Distribution cycle counts, end of year inventory and other accompanying data submitted to the DEA Compliance Group, to support the end of year report filing (1/31 letter). •Working closely with Distribution to gather data reflecting all shipments, receipts and destructions. Analyze the data for accuracy throughout the year and uses this information to generate ARCOS reports for periodic submission to DEA. •Interfacing with other departments such as Distribution, Customer Service, Sales, Security, Legal or IT to keep abreast of product, facility or process changes affecting the DEA compliance of our distribution facilities.•Completing DEA 106 theft/loss forms for in-transit theft/loss reporting to DEA. Partners with Security, Distribution and management as required to assist with investigative efforts and helps to monitor that any required corrective actions are implemented. •Completing DEA 222 order forms for signature by an authorized power of attorney, for the Distributor and Analytical DEA registrations. Record form information in the appropriate logbook for tracking purposes.•Interfacing with DEA as required on issues relating to reporting requirements and other miscellaneous requests.
  • Qualitest Pharmaceuticals
    Controlled Substance Coordinator
    Qualitest Pharmaceuticals Jul 2012 - Jul 2013
    Huntsville, Alabama Area
    •Responsible for following and upholding DEA regulations and educating coworkers to maintain compliance•Responsible for the monitoring of controlled substance processes to detect and deter potential diversion situations involving controlled substances•Responsible for all movement of controlled substances within the designated facilities. This involves the transport of product between Receiving, Vault or Cage, Production or Packaging, QC or R&D.•This position requires knowledge of DEA regulations and security requirements for controlled products, as well as knowledge of cGMP requirements. It requires a high level of honesty, integrity, and trustworthiness. It demands one to be extremely detail oriented, to maintain a high level of accuracy, and to be confident and assertive.

Brian Keel, Mba Skills

Gmp Pharmaceutical Industry Sop Fda 21 Cfr Part 11 Dea Quality Assurance Quality Control Regulatory Requirements Pharmaceutics Quality System Leadership Process Improvement Cross Functional Team Leadership Management Software Documentation Document Management Investigative Research Distribution Center Operations Security Drug Development Microsoft Office Training Team Building Manufacturing Internal Audit

Brian Keel, Mba Education Details

Frequently Asked Questions about Brian Keel, Mba

What company does Brian Keel, Mba work for?

Brian Keel, Mba works for Axient

What is Brian Keel, Mba's role at the current company?

Brian Keel, Mba's current role is Flight Test Analyst at Axient Corporation.

What is Brian Keel, Mba's email address?

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What is Brian Keel, Mba's direct phone number?

Brian Keel, Mba's direct phone number is +125624*****

What schools did Brian Keel, Mba attend?

Brian Keel, Mba attended Florida Institute Of Technology, Athens State University, Northeast Alabama Community College.

What skills is Brian Keel, Mba known for?

Brian Keel, Mba has skills like Gmp, Pharmaceutical Industry, Sop, Fda, 21 Cfr Part 11, Dea, Quality Assurance, Quality Control, Regulatory Requirements, Pharmaceutics, Quality System, Leadership.

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