Todd Outwin

FAQ About Todd Outwin

• What is Todd Outwin's address?

  Todd Outwin is located at
  Princeton, New Jersey, United States

• What is Todd Outwin's job title?

  Todd Outwin is a
  Pharmaceutical professional with a strong process development and analytical background, as well as a proven track record in new systems introduction, seeking role supporting compliant computer systems in the Life Science industry. • In-depth experience with Software Development Life-Cycle Management and established subject matter expert in equipment/instrument qualification, Computer System Validation, Good Manufacturing Practices and 21 CFR Part 11 compliance. • Implement and provide technical support for wide range of pharma processes and information management systems in current good manufacturing practice (cGMP) production areas through instituting interdepartmental project plan, managing multiple projects, overseeing qualification / test script execution, and training user department personnel on new systems. • Successfully resolved various quality issues during equipment qualification and computer validation test script execution. • Document and communicate technical information clearly and concisely for internal management, external vendors, contractors and user department personnel by authoring qualification protocols and reports, traceability matrices, standard operating procedures (SOP), requirement specifications (URS/SRS), and other. Bristol Myers Squibb

• What industry does Todd Outwin currently work in?

  Todd Outwin currently works in the
  Bristol Myers Squibb

• What is Todd Outwin's area of expertise?

  Todd Outwin specializes in
  Pharmaceutical professional with a strong process development and analytical background, as well as a proven track record in new systems introduction, seeking role supporting compliant computer systems in the Life Science industry. • In-depth experience with Software Development Life-Cycle Management and established subject matter expert in equipment/instrument qualification, Computer System Validation, Good Manufacturing Practices and 21 CFR Part 11 compliance. • Implement and provide technical support for wide range of pharma processes and information management systems in current good manufacturing practice (cGMP) production areas through instituting interdepartmental project plan, managing multiple projects, overseeing qualification / test script execution, and training user department personnel on new systems. • Successfully resolved various quality issues during equipment qualification and computer validation test script execution. • Document and communicate technical information clearly and concisely for internal management, external vendors, contractors and user department personnel by authoring qualification protocols and reports, traceability matrices, standard operating procedures (SOP), requirement specifications (URS/SRS), and other.

• Which languages does Todd Outwin speak? 

  Todd Outwin speaks the following languages:
  No languages available.

• Which industries has Todd Outwin previously worked in?

  Todd Outwin has prior experience in the following industries:
  Bristol Myers Squibb , Bayer Pharmaceuticals , Akorn , Sun Pharma , Sun Pharma , Sun Pharma , Colgate Palmolive , Johnson And Johnson , Johnson And Johnson Prd , Teva Pharmaceuticals , Teva Pharmaceuticals , Ciba , Ciba

• What is Todd Outwin’s work experience?  

  Todd Outwin has the following professional experience:
  Bristol Myers Squibb , Bristol Myers Squibb , Bayer Pharmaceuticals , Akorn , Sun Pharma , Sun Pharma , Sun Pharma , Colgate Palmolive , Johnson And Johnson , Johnson And Johnson Prd , Teva Pharmaceuticals , Teva Pharmaceuticals , Ciba , Ciba .

• How can I find Todd Outwin on LinkedIn?  

  You can view Todd Outwin’s
  LinkedIn profile at LinkedIn URL.

• What are Todd Outwin’s work email addresses?  

  Todd Outwin’s work email addresses are
  [email protected] .

• What company does Todd Outwin work for?  

  Todd Outwin works at
  Bristol Myers Squibb