PRINCIPAL, QA

Technical Resources International, Inc

• $120K — $145K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in a relevant field
  • Strong knowledge of current GCP regulations
  • Experience with regulatory authority inspections
  • Experience working with Quality Systems for CROs
  • Experience conducting GCP clinical site audits
  • Excellent written and verbal communication skills
  • Proficiency in MS Office

Responsibilities

  • Verify GCP compliance with SOPs and regulations
  • Conduct audits of clinical sites and vendors
  • Provide support to the Quality Management System
  • Lead external audits at clinical and vendor sites
  • Drive process improvement activities and CAPA investigations
  • Review clinical quality management plans and offer consultative support
  • Train junior staff on regulations and quality processes
  • Support regulatory authority inspections and business development activities

Benefits

  • Fully remote option for DMV area residents
  • Opportunity to lead process improvement initiatives
  • Engagement with regulatory authority inspections
  • Support for professional development through training
  • Involvement in business development activities
Full Job Description
Job Title

PRINCIPAL, QA

Location

Bethesda, MD 20817 US (Primary)

Category

Quality Assurance

Job Type

Full-Time

Salary Range

$120,000-$145,000

Education

Bachelor's Degree

Travel

Up to 25%

Job Description

  • Verifies GCP compliance to applicable Standard Operating Procedures (SOPs) and regulations
  • Conducts audits of clinical sites and vendors/suppliers
  • Provides full support to the Quality Management System
  • Conduct external audits at clinical sites and vendor sites
  • Leads process improvement activities and CAPA investigations
  • Reviews clinical quality management plans and provides consultative support to clinical sites (as applicable.
  • Trains junior staff on regulations and quality processes
  • Supports regulatory authority inspections
  • Supports business development activities, as requested


Job Requirements

  • Strong knowledge of current GCP regulations
  • Experience with regulatory authority inspections
  • Experience working with Quality Systems for CROs
  • Experience conducting GCP clinical site audits
  • Excellent written/verbal communication skills
  • Proficiency in MS Office
  • This role is fully remote for those living in the DMV area.


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