Richard J Maloney, PMP

Director at Daiichi Sankyo, Inc.
  • Claim this Profile
Contact Information
us****@****om
(386) 825-5501
Location
JE

Topline Score

Topline score feature will be out soon.

Bio

Generated by
Topline AI

You need to have a working account to view this content.
You need to have a working account to view this content.

Experience

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Director
      • Sep 2013 - Present

      Understand business demands, identify opportunities and deliver informatics solutions to address near and long term needs for business functions in the US, EU, and Japan. Establish and build collaborative relationships with stakeholders, strategic vendors and software providers. Understand business demands, identify opportunities and deliver informatics solutions to address near and long term needs for business functions in the US, EU, and Japan. Establish and build collaborative relationships with stakeholders, strategic vendors and software providers.

    • Switzerland
    • Biotechnology Research
    • 700 & Above Employee
    • Project Manager/ IT Analyst
      • Sep 2003 - Aug 2013

      Performed project and data management functions to plan, organize and manage resources for successful completion of Non-Clinical Safety (NCS) and R&D projects. Supported the day-to-day operation of various computer systems including global safety data system, Watson, PathData and eSirius. Performed project and data management functions to plan, organize and manage resources for successful completion of Non-Clinical Safety (NCS) and R&D projects. Supported the day-to-day operation of various computer systems including global safety data system, Watson, PathData and eSirius.

    • United States
    • Pharmaceutical Manufacturing
    • 400 - 500 Employee
    • Applications Specialist
      • Feb 2001 - Sep 2003

      Responsible for all phases of IT support for the Drug Safety department, including CSV, 21 CFR Part 11 compliance, system life cycle development and applications support and maintenance. Responsible for all phases of IT support for the Drug Safety department, including CSV, 21 CFR Part 11 compliance, system life cycle development and applications support and maintenance.

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • System Manager/ Chemist
      • Sep 1995 - Feb 2001

      Responsible for support and validation of computer systems within a GMP environment. Performed analytical testing of pre-marketed and marketed pharmaceutical products using standard laboratory equipment. Responsible for support and validation of computer systems within a GMP environment. Performed analytical testing of pre-marketed and marketed pharmaceutical products using standard laboratory equipment.

Education

  • Long Island University
    Master's degree, Computer Science
    1998 - 2000
  • NUI Galway
    Bachelor of Science (BSc), Science
    1989 - 1992
  • George Washington University
    Master's Certificate in IT Project Management
  • Liverpool John Moores University
    Bachelor's degree, Applied Chemistry

Community

You need to have a working account to view this content. Click here to join now