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Regulatory Operations Quality Control; FDA

Job in High Point, Guilford County, North Carolina, 27264, USA
Listing for: Advanced Personnel Resources, Inc.
Full Time position
Listed on 2026-02-13
Job specializations:
  • Healthcare
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Regulatory Operations Quality Control (FDA)

Advanced Personnel Resources has an immediate contract opening for a Regulatory Operations Quality Control (FDA) professional in Greensboro, NC (onsite).

Our client is seeking a detail-oriented and motivated Regulatory Operations QC Specialist to join their Regulatory Operations team. This role will focus on regulatory operations, quality control of submissions, documentation, and regulatory research, not scientific study design or data generation. The assignment is indefinite
.

Schedule: Monday–Friday | 8:00 AM–5:00 PM

Employment Type: Indefinite Contract

Pay: $20-40

Benefits offered by APR: Medical, Dental, Term Life, Short-Term Disability, Holiday Pay, Service Bonus, Direct Deposit

The ideal candidate is a technically inclined administrative professional with regulatory experience who is comfortable researching FDA and state-level requirements, quality-checking submissions and narratives, and helping establish standardized business processes.

Key Responsibilities
  • Quality control (QC) of regulatory submissions, narratives, and supporting documentation
  • Research and interpret FDA guidelines and state-specific regulatory reporting requirements
  • Navigate FDA websites and regulatory resources to locate and interpret applicable requirements
  • Collect, organize, and manage regulatory documents and data
  • Support development, writing, and maintenance of SOPs and business processes
  • Ensure Regulatory Science team submissions align with applicable regulatory requirements
  • Assist with process improvements and workflow optimization within Regulatory Operations
Qualifications
  • Regulatory experience highly preferred (Regulatory Affairs, Regulatory Operations, Regulatory Science, or related)
  • Strong administrative and technical documentation skills
  • Experience QC’ing regulatory submissions or similar compliance documentation
  • Comfortable researching and interpreting regulatory guidelines
  • Detail-oriented with strong organizational and analytical skills
  • Team-oriented, professional communicator with tact and diplomacy
  • Self-starter with a “go-getter” mindset and willingness to learn
Education
  • Associate’s or Bachelor’s degree

Please attach your resume (MSWord if possible) to submission.

All inquiries are highly confidential and go directly to:

Misty Davis | Advanced Personnel Resources |

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