Rebecca Connors

Vice President, Quality at Particle Dynamics
  • Claim this Profile
Contact Information
us****@****om
(386) 825-5501
Location
Bloomington, Indiana, United States, IN
Skills

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

Credentials

  • Preventative Controls Qualified Individual (PCQI)
    Food Safety Preventive Controls Alliance (FSPCA)

Experience

  • Particle Dynamics
    • United States
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Vice President, Quality
      • May 2016 - Present

      Vice President of Quality in a cGMP manufacturing organization. Responsible for all Quality related activities in two facilities (Seymour, IN and St. Louis, MO). Vice President of Quality in a cGMP manufacturing organization. Responsible for all Quality related activities in two facilities (Seymour, IN and St. Louis, MO).

  • Cook Pharmica
    • United States
    • Biotechnology Research
    • 1 - 100 Employee
    • QC Chemistry Manager
      • Jun 2011 - Apr 2016

      QC Manager in a cGMP, GLP compliant laboratory atmosphere supporting drug substance and drug product production. Responsible for, and manage, four QC departments (In-Process, Finished Product, Stability, and Method Validation/Transfer). QC Manager in a cGMP, GLP compliant laboratory atmosphere supporting drug substance and drug product production. Responsible for, and manage, four QC departments (In-Process, Finished Product, Stability, and Method Validation/Transfer).

  • Baxter International Inc.
    • United States
    • Medical Equipment Manufacturing
    • 700 & Above Employee
    • QC Laboratory Supervisor
      • Jul 2002 - Jun 2011

      QC Supervisor in a cGMP, GLP compliant pharmaceutical laboratory serving over 150 active clients. Responsible for releasing raw material, in-process, finished product and stability drug substance to ensure purity and compliance with FDA requirements. QC Supervisor in a cGMP, GLP compliant pharmaceutical laboratory serving over 150 active clients. Responsible for releasing raw material, in-process, finished product and stability drug substance to ensure purity and compliance with FDA requirements.

Education

  • Indiana University
    BS, Biology, Chemistry
    1997 - 2001

Community

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