Mitchell Cyran

About Mitchell Cyran

Dedicated pharmaceutical professional with 10 years of experience in a cGMP environment managing large and small molecule stability projects with 3 years of leadership experience. Skilled in directing stability studies through all stages of development with a strong focus on process improvement, staff training, and collaboration. Proven ability to work independently and as part of a team. Known for adaptability, reliability, and being detail oriented.

Experience

1. Qc Technical Resources and Compliance Specialist

   Novartis

   Jan 2025 — Present · Durham, NC, US

   Authors QC investigations and meets all targets for timely closure and CAPA completion.Coordinate with Quality to ensure compliance and continuous improvement in the QC labs.Plans and executes change control for method related changes.Performs technical review of QC assays as needed for cGMP release and characterization testing, including but not limited to cell-based methods (potency, AA), PCR (ddPCR, qPCR), Immunoassays (ELISA), chromatography (HPLC-UV, HPLC-ELSD, HPLC-MS), AUC, compendial assays (Bioburden, pH) and electrophoresis (CE, Western Blot).Authors technical documents such as Protocols / ReportsSupports regulatory inspections

Education

• Mercer County Community College

  Pre-Pharmacy Studies

  2007 — 2008

• Palm Beach Atlantic University

  B.S., Medicinal & Biological Chemistry

  2008 — 2010

• The College of New Jersey

  Psychology

  2006 — 2007

Skills

• Gmp
• Uv/Vis
• Hplc
• Titration
• Centrifugation
• Gas Chromatography
• Word
• Ph Meter
• Pharmaceutics
• Chemistry
• Microsoft Word
• Good Laboratory Practice (Glp)
• U.s. Food and Drug Administration (Fda)
• Wet Chemistry
• Powerpoint
• Microsoft Excel
• Distillation
• Pharmaceutical Industry
• Sop
• Laboratory
• Excel
• Gc/Ms
• Analytical Chemistry
• Lims