Kerri Molitor

Quality Program Manager, Distribution

Role
Quality Program Manager, Distribution at Medtronic
Location
Minneapolis, MN, US
LinkedIn followers
500 followers

About Kerri Molitor

Knowledge of 21 CFR parts 11, 210, 211 and 820, ISO 13485 • Directly involved in a…

Experience

  1. Quality Program Manager, Distribution

    Medtronic

    Jul 2014 — Present

Education

  • Augsburg University

    BA Biology

Skills

  • Gamp
  • Standard Operating Procedure (Sop)
  • Medical Devices
  • Capa
  • Software Documentation
  • Manufacturing
  • U.s. Food and Drug Administration (Fda)
  • Change Control
  • Quality Management
  • Biopharmaceuticals
  • Fda Gmp
  • Lims
  • Quality Assurance
  • Validation
  • Trackwise
  • Quality System
  • V&V
  • Iso 13485
  • Biotechnology
  • Cross-Functional Team Leadership
  • Iso 14971
  • 21 Cfr Part 11
  • Regulatory Requirements
  • Pharmaceutical Industry
  • Sop
  • Fda
  • Contract Manufacturing
  • Glp
  • Computer System Validation
  • Technology Transfer
  • 21 Cfr
  • Sap
  • Gxp
  • Quality Auditing
  • Regulatory Affairs
  • Design Control
  • Quality Control
  • Gmp
  • Testing

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Kerri Molitor — Quality Program Manager, Distribution at Medtronic in Minneapolis, MN, US | Unifers