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Sr. QC Systems Specialist

Job in Social Circle, Walton County, Georgia, 30279, USA
Listing for: Stellent IT LLC
Full Time position
Listed on 2026-07-04
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Engineering, Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below
Location: Social Circle

Sr. Quality Control Systems Specialist.

100% ONSITE in Social Circle, GA.

Job Description Senior Quality Control Specialist

Onsite - 100%

Summary of the Role:

This position functions as the technical and quality systems leader within QC Operations Support, responsible for:

  • Perform Compendial Assessments
  • Author and Review Technical Documents
  • Design and Coordinate Analytical Method Onboarding Activities
  • Lead Qualification of Critical Materials, Instruments, and Equipment
  • Oversee Change Control Management
  • Manage Corrective and Preventive Actions (CAPAs)
  • Serve as Subject Matter Expert (SME)
  • Collaborate Across Departments
  • Drive Continuous Improvement Initiatives
  • Conduct Data Trending and Analysis
  • Represent QC on Global and Local Projects
  • Perform Other Duties Assigned by Leadership
Education and Experience Requirements:
  • Requires bachelor's degree in science, engineering or other related technical field. 4+ years of related experience in pharmaceutical or similar regulated industry.
  • Strong QC Microbiology experience preferred (testing, sampling, processes)
Key Skills, Abilities, and

Competencies:
  • Must know quality laboratory operations and government regulations pertaining to pharmaceutical and medical device manufacturing labs.
  • Must have the ability to manage multiple tasks and responsibilities for the QC Lab.
  • Must have the ability of managing complex projects and resolving complex lab issues.
  • Must possess excellent technical and interpersonal skills, and be able to communicate with all level personnel and regulatory authorities.
  • Should have advanced knowledge in Statistical Analysis and cGMP standards. Strong leadership, project and people management skills, and ability to make critical decisions.
  • Strong understanding of business and/or industry.
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