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Vendor Surveillance Inspector Jobs in Raleigh, NC

Maintains surveillance by monitoring cameras and taking routine walks through the facility ... Conducts inspection of personal belongings or packages being carried into and out of the facility ...

Unarmed Security Lieutenant

Cary, NC

$15 - $17.75/hr

Visitor and vendor check-in procedures * Contractor verification * Vehicle and delivery inspections ... Coordinate investigations into internal or external security incidents. 4. Patrol & Surveillance ...

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Vendor Surveillance Inspector information

What is a vendor surveillance inspector?

Vendor Surveillance Inspectors are professionals responsible for monitoring and assessing vendors or suppliers to ensure they meet contractual, regulatory, and quality requirements. They conduct inspections, audits, and reviews of vendor facilities, processes, and products to verify compliance with industry standards and client specifications. Their work helps maintain product quality, reduce risks, and ensure timely delivery of goods or services. Vendor Surveillance Inspectors play a crucial role in industries such as manufacturing, construction, and energy, where supplier performance directly affects project success.

What are the key skills and qualifications needed to thrive as a vendor surveillance inspector, and why are they important?

To thrive as a Vendor Surveillance Inspector, you need a solid understanding of quality assurance, inspection protocols, and industry-specific standards, often supported by relevant technical degrees or certifications. Familiarity with inspection tools, non-destructive testing (NDT) methods, and reporting systems like ISO 9001 is typically required. Strong attention to detail, effective communication, and problem-solving abilities help inspectors work efficiently with vendors and ensure compliance. These skills are crucial for maintaining product quality, safety, and adherence to contractual and regulatory requirements.

What are some common challenges faced by vendor surveillance inspectors when monitoring supplier compliance, and how can these be addressed?

Vendor Surveillance Inspectors often encounter challenges such as inconsistent supplier documentation, varying quality standards across vendors, and communication barriers due to geographic or language differences. Addressing these issues typically involves establishing clear inspection protocols, maintaining regular communication with suppliers, and utilizing standardized checklists and reporting tools. Proactive relationship-building and ongoing training also help ensure that vendors understand compliance expectations and are prepared for inspections.

What is the difference between Vendor Surveillance Inspector vs Quality Control Inspector?

AspectVendor Surveillance InspectorQuality Control Inspector
CertificationsOften requires certifications like ASQ CQI, ISO auditorMay require certifications like ASQ CQI, ISO auditor
Work EnvironmentPerforms inspections at supplier sites and manufacturing facilitiesWorks mainly within manufacturing or production facilities
Industry UsageCommonly used in supply chain and procurement processesUsed across various manufacturing sectors for product quality

Both roles require similar certifications and often overlap in work environment and industry usage. However, Vendor Surveillance Inspectors focus on monitoring supplier compliance and quality at external sites, while Quality Control Inspectors typically perform inspections within manufacturing facilities to ensure product standards.

What are popular job titles related to Vendor Surveillance Inspector jobs in Raleigh, NC?

For Vendor Surveillance Inspector jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Vendor Surveillance Inspector jobs in Raleigh, NC look for?

The top searched job categories for Vendor Surveillance Inspector jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Vendor Surveillance Inspector jobs?

Cities near Raleigh, NC with the most Vendor Surveillance Inspector job openings:

Associate Clinical Safety Surveillance Director

Scorpion Therapeutics

Chapel Hill, NC โ€ข On-site

$180 - $240/hr

Other

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Job description

Associate Clinical Safety Surveillance DirectorResponsibilities
  • Oversee management of SAEs and events of special interest across UT sponsored clinical trials; provide strategic direction to team and vendors to improve efficiency, quality, and compliance.
  • Support safety governance, inspection readiness, and sustained regulatory compliance for the UT Sponsored Clinical Trial portfolio.
  • Evaluate and execute process changes in response to regulatory updates for end-to-end SAE and AESI handling.
  • Maintain and monitor unified SAE/AESI handling operating procedures (e.g., Safety Management Plan); ensure processing/submission per UT SOPs and industry standards.
  • Provide strategic guidance for developmental PV case management and reporting of ICSSRs.
  • Serve as main point of contact for day-to-day questions and issue escalation on SAE/AESI handling; manage GPS clinical trial oversight team metrics.
  • Develop and deliver training/materials for SAE/AESI handling; lead direct reports (training, performance, coaching/mentoring, career development, recruitment support as needed).
  • Lead inspection/audit readiness; perform root cause analysis and ensure CAPA; review/approve deviations/CAPAs.
  • Develop and implement new/revised SOPs; update procedural documents for SAE/AESI case handling.
  • Stay current on global/local GCP and GVP regulations supporting clinical trials in PV.
Minimum Requirements
  • BS in related field or BSN with 12+ years, or MS with 10+ years, or PharmD/PhD/MD/DO (or international equivalent) with 7+ years in pharmacovigilance end-to-end ICSR case processing.
  • 5+ years vendor management and/or CT oversight; 5+ years clinical trial or product development.
  • 3+ years people management.
  • Argus experience (preferred) and/or other safety databases.
  • End-to-end case processing (data entry, QC, medical review, regulatory submissions).
  • Project management; drug development and registration safety knowledge; global regulations/guidelines; MedDRA coding; strong written/verbal and analytical skills; cross-functional effectiveness; ability to challenge current state; adaptable in ambiguity.
  • Prior clinical PV management experience.
Job Location/Work Schedule
  • Durham, NC office with hybrid schedule (at least 3 days in office each week).
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