Beckie Ellis

Senior Vice President, Global Regulatory Affairs & Quality Assurance

Beckie Ellis is Senior Vice President, Global Regulatory Affairs and Quality Assurance and has global responsibility for plant Quality Assurance, global Quality Systems’ development, Regulatory Compliance, Certifications, Submissions and Approvals.

Beckie is an internationally experienced RAQA professional with diversified knowledge and skills that cover more than 25 years of Quality Systems, Process Improvement, Sterilization Validation and New Product Development experience in both the medical device and pharmaceutical industries. She has worked for such companies as NeoRx, Fuller Laboratories/Parke-Davis, International Isotopes, Medical Incorporated, St. Jude Medical, and OsteoMed before joining the Argon team. These organizations cross a variety of product platforms including kidney dialysis, brachytherapy products, radiopharmaceuticals, heart valves, vascular grafts, arterial and cardiotomy blood filters, breast implants and orthopedic implants.

During her career Ms. Ellis has worked overseas where she oversaw the relocation of a mini-assembly plant in Rio de Janeiro, Brazil and served as Operations Manager for a heart valve manufacturing facility in Perth, Australia.

She holds a B.S. in Microbiology as well as an M.B.A. in Operations Management from the University of Minnesota, and has achieved a Master’s Certificate in Organizational Leadership from Villanova. She has her RAC from RAPS and is certified as a CQA, CSSGB, CQE, CQIA and CQM/OE from the American Society for Quality.

On a personal note, Ms. Ellis has held volunteer leadership positions for the ASQ Biomedical Division and Dallas Section of ASQ and currently serves as the ASQ representative to the FDA/Medical Device Industry Coalition in Dallas, TX. She also served two years as a site examiner with Quality Texas for the Texas Quality Award.

Beckie Ellis
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