Suhail Abdullah

Regulatory Affairs Specialist | Master of Business and Science

Role
Senior Principal Regulatory Affairs Specialist at New World Medical
Location
Fontana, CA, US
LinkedIn followers
500 followers
Manufacturing & ProductionView LinkedIn profile

About Suhail Abdullah

Key Strengths • Versatile, motivated, and proactive problem solver with a comprehensive understanding of medical device strategy and product development. Known for leading new initiatives, risk taking, strategy, deal making, planning, project management, and making innovative contributions. • Accomplished team oriented professional and independent thinker with strong leadership experience serving as a resource to multiple functions. • Successful oversight of product development and launch efforts Core Competencies • Technology scouting, business strategy, business development, competitive analysis, project management, regulatory affairs and submissions, product development and launch, test method development, design requirements and specification, risk management and FMEA, pre-clinical studies, clinical/medical affairs, medical education, IFU writing, publications, KOL management, grant writing, SOP writing, glaucoma surgical devices, detail oriented, strong writing and presentation skills.

Experience

  1. Senior Principal Regulatory Affairs Specialist

    New World Medical

    Jan 2023 — Present · CA, US

Education

  • Keck Graduate Institute

    Master of Business and Science

    2003 — 2005

  • University of California, Los Angeles

    Bachelors

    1998 — 2002

Skills

  • Product Management
  • Commercialization
  • Market Development
  • Cross-Functional Team Leadership
  • Fda
  • R&D
  • Project Management
  • Lifesciences
  • Biotechnology
  • Iso 13485
  • Regulatory Affairs
  • Product Development
  • Ce Marking
  • U.s. Food and Drug Administration (Fda)
  • Ophthalmology
  • Design Control
  • Life Sciences
  • Product Launch
  • Qsr 820
  • Pharmaceutical Industry
  • Process Improvement
  • Testing
  • Technical File, Dmr and Preparing Sops, Work Instructions
  • Cad (Autodesk Inventor)
  • Medicine
  • Medical Devices
  • Research and Development (R&D)
  • Risk Management Iso 14971
  • Medical Device Design Controls

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