Kevin Staffin

Associate Director, GMP QA at Nuvalent

Kevin Staffin has been working in the quality assurance field for over 10 years. Kevin started their career as a QA Engineer at ZOLL Medical Corporation before moving on to Shire HGT, where they eventually became a Supervisor in Quality Assurance. Kevin then spent a year as the QA Manager at Anika Therapeutics before taking on a role as Associate Director of QA Tech Transfer at Shire. In 2019, Kevin became the Head of MA Bio Ops QA New Product Introduction at Takeda. Kevin is currently working as the Associate Director of GMP QA at Nuvalent. Throughout their career, Kevin has demonstrated a commitment to ensuring that products meet high standards of quality and compliance with established guidelines. Kevin is constantly looking for ways to improve quality assurance practices and make efficient use of staff resources. Kevin is dedicated to their work and takes pride in ensuring that customers are satisfied with the products they receive.

Kevin Staffin has a Masters in Quality Assurance and Regulatory Affairs from Temple University as well as a Bachelors in Biology from Grove City College. Kevin also attended Faith Heritage School.

Some of their coworkers include Allison Magnan - Associate Director, GCP Quality Assurance, Morgan Maiola - Senior Associate, Quality Assurance. Their manager is Kristi Byrnes, Director, Quality Assurance.

Links

Previous companies

Anheuser-Busch InBev logo
Anika Therapeutics logo
Pfizer logo
Bristol-Myers Squibb logo
ZOLL Medical Corporation logo

Timeline

  • Associate Director, GMP QA

    Current role

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