QA Compliance Lead Auditor
San Diego, CA 
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Job Description
Job Overview:

Labcorp Drug Development is seeking candidates for a QA Compliance Lead Auditor. The QA Compliance Lead Auditor will be remotely located (home-based) anywhere within the United Sates.

  • Conduct work as identified on the audit activity table (listing on table is not all inclusive but a representative sample)
  • Takes lead in generation of global QA policies on interpretation/ application of regulations
  • Provide subject matter expertise and leads/influences the ED/CS/CDS/CLS organization by providing guidance and client/authority facing support on specific niche regulatory topics
  • Hosts (i.e. for cause inspection, non-standard authority inspections, country-specific or scope of inspection) external audits/inspections e.g. regulatory inspections, strategic clients.
  • Facilities and reviews responses to the audit.
  • Leads the reporting of quality metrics and implementation of necessary corrective actions and/or process improvements via appropriate forum (e.g. Monthly Reports, Site Quality Review, Liaison meetings).
  • Manage (for own area of expertise) / participate (for multi-regulatory topics) in broad scope global Quality initiative(s) aimed at improving compliance and/or efficiency of the QA organization
  • Acts as a backup for QA Manager; provides monthly report of activities to QA Manager; performs other related duties as assigned
  • Ensure Regulatory Compliance and Quality Assurance (RC&QA) responsibilities, as indicated in applicable controlled documents, are followed
  • Other duties as assigned by management.
  • Regional travel essential with respect to adhering to pandemic restrictions.

Education/Qualifications:
  • A minimum of a Bachelor's Degree in a Pharmacy, Chemistry or Biology related discipline.
  • Postgraduate degree (MSC or equivalent) in science or management related discipline, preferable.
  • Experience may be substituted for education.
Experience:
  • 8 years in regulatory environment (experience in GXP roles).
  • GCP Phase II/IV experience: investigator site audits, vendors, project, process audits.
  • Regulatory expertise - detailed knowledge of specific regulation/ multiple regulations.
  • Experienced Lead Auditor.
  • Strategic communication with clients.
  • Experience leading process improvement initiatives.

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Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us.

 

Job Summary
Start Date
As soon as possible
Employment Term and Type
Regular, Full Time
Required Education
Bachelor's Degree
Required Experience
8+ years
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