Sheila S Bruschi

age ~43

from San Diego, CA

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Also known as:
  • Sheila Mariano Singson
  • Sheila M Singson
Phone and address:
2641 Lange Ave, San Diego, CA 92122
6502188928
Related to:
Connected to:

Sheila Bruschi Phones & Addresses

  • 2641 Lange Ave, San Diego, CA 92122 • 6502188928
  • Torrance, CA
  • Gardena, CA
  • Poway, CA
  • La Jolla, CA
  • 2641 Lange Ave, San Diego, CA 92122

Work

  • Company:
    Nuvasive, inc.
    Jul 2009
  • Position:
    Associate manager, regulatory affairs

Education

  • Degree:
    B.S.
  • School / High School:
    University of California, San Diego
    1999 to 2003
  • Specialities:
    Bioengineering

Skills

Medical Devices • Fda • Regulatory Affairs • Design Control • Iso 13485 • Biotechnology • Cross Functional Team Leadership • Capa • Biomedical Engineering • Quality System • Validation • Gmp • Life Sciences • Product Launch • Product Development • Clinical Trials • Commercialization • U.s. Food and Drug Administration • V&V • Gcp • Clinical Development • Pharmaceutical Industry • R&D • Lifesciences • Quality Auditing • Quality Assurance • Iso 14971 • Verification and Validation • Biomaterials • Orthopedic • Stem Cells • Regulatory Submissions • Biologics • Biocompatibility • Regulatory Requirements • Spine • Glp • Biopharmaceuticals • Research and Development • Orthopedics • Corrective and Preventive Action • Technology Transfer

Industries

Medical Devices

Resumes

Sheila Bruschi Photo 1

Director, Regulatory Affairs

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Location:
San Diego, CA
Industry:
Medical Devices
Work:
NuVasive, Inc. since Jul 2009
Associate Manager, Regulatory Affairs
Cytori Therapeutics Nov 2004 - Jul 2009
Regulatory Associate II
CTS Aug 2003 - Aug 2004
Quality Specialist
Education:
University of California, San Diego 1999 - 2003
B.S., Bioengineering
Skills:
Medical Devices
Fda
Regulatory Affairs
Design Control
Iso 13485
Biotechnology
Cross Functional Team Leadership
Capa
Biomedical Engineering
Quality System
Validation
Gmp
Life Sciences
Product Launch
Product Development
Clinical Trials
Commercialization
U.s. Food and Drug Administration
V&V
Gcp
Clinical Development
Pharmaceutical Industry
R&D
Lifesciences
Quality Auditing
Quality Assurance
Iso 14971
Verification and Validation
Biomaterials
Orthopedic
Stem Cells
Regulatory Submissions
Biologics
Biocompatibility
Regulatory Requirements
Spine
Glp
Biopharmaceuticals
Research and Development
Orthopedics
Corrective and Preventive Action
Technology Transfer
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