Linda Nevins

Director, Global Quality Auditing and Due Dilligence Services at Teva Pharmaceuticals

Role
Global Quality and Compliance Director at Teva Pharmaceuticals
Location
Caldwell, NJ, US
LinkedIn followers
500 followers
Manufacturing & ProductionView LinkedIn profile

About Linda Nevins

Highly motivated Quality professional who strives to dilligently protect the consumer through implementation and assurance of quality systems and compliance to health regulations globally in the workplace and in Third Party Organizations/External Contractors.

Experience

  1. Global Quality and Compliance Director

    Teva Pharmaceuticals

    Jan 2014 — Present · Parsippany, NJ, US

    Name change: Actavis became Allergan post acquisition.

Education

  • Fairleigh Dickinson University

    MBA, International Business/Trade/Commerce

    1995 — 1999

  • Lakeland Regional High School

    Diploma

  • Temple University

    Certified, Pharmaceutical Studies-QA/RA

    2007 — 2010

  • Montclair State University

    B.S., Human Ecology/Nutrition

Skills

  • Gmp
  • Standard Operating Procedure (Sop)
  • Change Control
  • Compliance Operations
  • Capa
  • U.s. Title 21 Cfr Part 11 Regulation
  • Trackwise
  • Pharmaceutical Industry
  • Sop
  • Fda
  • 21 Cfr Part 11
  • Stability Studies
  • Consent Decree
  • Computer System Validation
  • Biopharmaceuticals
  • Gxp
  • Quality Auditing
  • Aseptic Processing
  • Cleaning Validation
  • Pharmaceutics
  • Validation
  • U.s. Food and Drug Administration (Fda)
  • Quality System
  • Regulatory Guidelines
  • Quality Assurance
  • Quality Management
  • Gamp

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Linda Nevins — Global Quality and Compliance Director at Teva Pharmaceuticals in Caldwell, NJ, US | Unifers