Karen Mullin

Associate Director, Quality Assurance at Avidity Biosciences, Inc.

Role
Associate Director, Quality Assurance at Avidity Biosciences, Inc.
Location
Boston, MA, US
LinkedIn followers
500 followers
Information TechnologyView LinkedIn profile

About Karen Mullin

I have more than 20 years of industry experience with 18 years supporting cGMP operations from both a Quality Assurance/Compliance and a Validation perspective. My experiences in industry have encompassed a broad range of evolving opportunities to develop and build on my skill set. My strengths and passions are focused on working with and organizing cross-functional teams to develop and ensure the highest levels of compliance and efficiency in developing quality systems.In Regulatory Affairs, I hold a Dual Certificate, Pharmaceuticals and Medical Devices from RAPS Online University.

Experience

  1. Associate Director, Quality Assurance

    Avidity Biosciences, Inc.

    Aug 2022 — Present · San Diego, CA, US

Education

  • Oakland University

    Master of Science (MS), Analytical Chemistry

    2000 — 2002

  • Oakland University

    B.S; B.S, Chemistry; Chemistry; organic and analytical chemistry

    1995 — 1999

Skills

  • Biotechnology
  • Change Control
  • Quality Control
  • Gmp
  • Technology Transfer
  • Glp
  • Software Documentation
  • Capa
  • Quality Assurance
  • Pharmaceutical Industry
  • Sop
  • Fda
  • Chromatography
  • Compliance
  • Analytical Chemistry
  • Regulatory Affairs
  • Regulatory Submissions
  • V&V
  • Hplc
  • Good Laboratory Practice (Glp)
  • Cgmp
  • Standard Operating Procedure (Sop)
  • Validation

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Karen Mullin — Associate Director, Quality Assurance at Avidity Biosciences, Inc. in Boston, MA, US | Unifers