![How One Brand Solved the Marketing Attribution Puzzle [Video]](https://contentmarketinginstitute.com/wp-content/uploads/2025/03/marketing-attribution-model-600x338.png?#)
![Building A Digital PR Strategy: 10 Essential Steps for Beginners [With Examples]](https://buzzsumo.com/wp-content/uploads/2023/09/Building-A-Digital-PR-Strategy-10-Essential-Steps-for-Beginners-With-Examples-bblog-masthead.jpg)
![How to Use GA4 to Track Social Media Traffic: 6 Questions, Answers and Insights [VIDEO]](https://www.orbitmedia.com/wp-content/uploads/2023/06/ab-testing.png)
![[HYBRID] ?? Graphic Designer](https://a5.behance.net/cbf14bc4db9a71317196ed0ed346987c1adde3bb/img/site/generic-share.png)
North Carolina Licensed Safety Specialist
A company is looking for a Safety Specialist / Quality and Training Specialist (QTS). Key Responsibilities Support management with the maintenance and review of quality documents and ensure team training on client SOPs Design and implement training programs, conduct onboarding sessions, and monitor employee quality performance Oversee quality assurance, compliance, and audit support activities, ensuring adherence to industry regulations Required Qualifications Bachelor's or master's degree in Pharmacy or Life Sciences 7+ years of relevant work experience in pharmacovigilance 5+ years in a quality role within the pharmaceutical or biotechnology industry Strong knowledge of worldwide GPV regulations and experience with audits and inspections Advanced knowledge of quality management systems and electronic systems in regulated environments
A company is looking for a Safety Specialist / Quality and Training Specialist (QTS).
Key Responsibilities
Support management with the maintenance and review of quality documents and ensure team training on client SOPs
Design and implement training programs, conduct onboarding sessions, and monitor employee quality performance
Oversee quality assurance, compliance, and audit support activities, ensuring adherence to industry regulations
Required Qualifications
Bachelor's or master's degree in Pharmacy or Life Sciences
7+ years of relevant work experience in pharmacovigilance
5+ years in a quality role within the pharmaceutical or biotechnology industry
Strong knowledge of worldwide GPV regulations and experience with audits and inspections
Advanced knowledge of quality management systems and electronic systems in regulated environments