Chandresh Patel

FAQ About Chandresh Patel

• What is Chandresh Patel's address?

  Chandresh Patel is located at
  Somerset, New Jersey, United States

• What is Chandresh Patel's job title?

  Chandresh Patel is a
  • More than twenty five years of combined experience in pharmaceutical, oncology and biotechnology operations. Network leadership role. Responsible for rollout of global Readily Apparent Assignable Cause (RAAC) LIR workflow in gQTS (TrackWise). Excellent communication and problem solving skills. • QA and QC Responsibilities: Global Change Management, Quality Metrics Reporting, Managing Lab operations, Investigations, Effective CAPA implementation, Audits, Technical Reports, SOPs and LAB documents. Review compendia changes and corporate policies and/or quality standards affecting site documents. Inspection Readiness. • Collaborate with applicable team members or other department/division in a cross-functional meeting to resolve scientific and technical investigation related issues and implement effective CAPA and thereby reducing number of investigations. • Provide quality support during numerous BOHs inspections, corporate audits: Inclusive of Pre-approval inspection for ANDA pharmaceuticals, oncology (NDA) and vaccine products (NDA), General GMP Audits/Inspection and post-marketing commitments. Bristol Myers Squibb

• What industry does Chandresh Patel currently work in?

  Chandresh Patel currently works in the
  Bristol Myers Squibb

• What is Chandresh Patel's area of expertise?

  Chandresh Patel specializes in
  • More than twenty five years of combined experience in pharmaceutical, oncology and biotechnology operations. Network leadership role. Responsible for rollout of global Readily Apparent Assignable Cause (RAAC) LIR workflow in gQTS (TrackWise). Excellent communication and problem solving skills. • QA and QC Responsibilities: Global Change Management, Quality Metrics Reporting, Managing Lab operations, Investigations, Effective CAPA implementation, Audits, Technical Reports, SOPs and LAB documents. Review compendia changes and corporate policies and/or quality standards affecting site documents. Inspection Readiness. • Collaborate with applicable team members or other department/division in a cross-functional meeting to resolve scientific and technical investigation related issues and implement effective CAPA and thereby reducing number of investigations. • Provide quality support during numerous BOHs inspections, corporate audits: Inclusive of Pre-approval inspection for ANDA pharmaceuticals, oncology (NDA) and vaccine products (NDA), General GMP Audits/Inspection and post-marketing commitments.

• Which languages does Chandresh Patel speak? 

  Chandresh Patel speaks the following languages:
  No languages available.

• Which industries has Chandresh Patel previously worked in?   

  Chandresh Patel has prior experience in the following industries:
  Silarx Pharmaceuticals

• What is Chandresh Patel’s work experience?  

  Chandresh Patel has the following professional experience:
  Bristol Myers Squibb , Pfizer , Pfizers Global Manufacturing Specialtybiotechnology Operating Unit , Silarx Pharmaceuticals .

• How can I find Chandresh Patel on LinkedIn?  

  You can view Chandresh Patel’s
  LinkedIn profile at LinkedIn URL.

• What are Chandresh Patel’s work email addresses?  

  Chandresh Patel’s work email addresses are
  [email protected] .

• What company does Chandresh Patel work for?  

  Chandresh Patel works at
  Bristol Myers Squibb