Allison (Withers) Gecik, RAC has a diverse work experience in the field of regulatory affairs and quality management. Allison began their career as a Physical Therapy Aide at Orthopedic Care Physical Therapy Center in 2003 and worked there until 2011. In 2011, they joined Zimmer Trabecular Metal Technology as a Regulatory Affairs Associate and later became a Senior Regulatory Associate in 2014. Allison then worked as a Regulatory Affairs Project Manager at Zimmer Biomet - Trabecular Metal Technology from 2017 to 2018. Since 2018, they have been working at b-ONE Ortho, Corp. where they started as a Regulatory Affairs Manager and was promoted to Associate Director Regulatory Affairs in 2020. Currently, they hold the position of Director, Quality and Regulatory.
Allison (Withers) Gecik, RAC completed their Bachelor of Science (B.S.) degree in Biomedical/Medical Engineering from Rutgers University, where they studied from 1999 to 2003. Allison further pursued their education by obtaining multiple certifications in regulatory affairs. In December 2014, they completed the Regulatory Affairs Certification Program's RAC-US certification. Additionally, they obtained the Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professionals Society (RAPS) in December 2014 and again in November 2017.
March, 2022 - present
March, 2020
January, 2018
Director-Quality and Regulatory at SigTuple
Director, Quality and Regulatory Affairs at QMENTA
Director Quality And Regulatory Compliance at Cancer Research And Biostatistics (CRAB)
Director - Quality And Regulatory Affairs at Piramal Pharma Solutions
Director Quality And Regulatory at Rarity Bioscience