QVR recruits talent in these key skill disciplines:

Quality

  • CAPA / Root Cause
  • 483 / Consent
  • Deviation Management
  • Process Improvement
  • eQMS implementation
  • SOP / Documentation Generation
  • Batch / Deviation Review

Validation

  • IQ/OQ/PQ for Process Validation
  • IQ/OQ/PQ for Cleaning Validation
  • URS Requirements
  • Aseptic
  • Equipment Packaging
  • Protocol Writing
  • CQV / FAT

Regulatory

  • Submission Management (IND/NDA)
  • Dossier Compilation
  • Compliance Remediation
  • Regulatory Strategy
  • Regulatory Labeling
  • EU MDR Upgrades
  • Post Approval Maintenance

Why choose QVR?

Flexibility

Project outsourcing. Consulting. Contract staffing. We provide resources in a manner that best matches each client’s distinct needs. That means we give our clients greater project control, less risk and a better cost structure than traditional outsourcing or staffing solutions.

Domain Expertise

QVR offers national consulting support. We are experts in the Quality, Validation and Regulatory fields and have successfully completed engagements with over 200 different pharmaceutical clients.

Speed

Because of the talent we have on staff and in our network, we are able to provide technical resources faster in our core areas…typically in 24 to 48 hours.


Delivery Models


Project Staffing

SHORT AND LONG-TERM CONSULTANTS.

We provide talent to supplement your team, and support your organization’s clinical trials research and rescue projects.


Life Sciences Recruiting

CONTRACT-TO-HIRE AND DIRECT HIRE RECRUITING.

QVR will shorten your search for top performing Life Sciences professionals and directly recruit talent from places you can’t recruit.


Project & FSP Solutions

CLINICAL TRIALS CONSULTING AND OUTSOURCING.

Through our sister division, Vita Data Sciences, we provide end-to-end data management and biometric services, strategic consulting, and our unique Functional Service Provider model.