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Quality Assurance Compliance Specialist

Job in Camden, Camden County, New Jersey, 08100, USA
Listing for: ClinLab Solutions Group
Full Time position
Listed on 2026-09-20
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Engineering
Salary/Wage Range or Industry Benchmark: 75000 - 110000 USD Yearly USD 75000.00 110000.00 YEAR
Job Description & How to Apply Below

Work Location: Mercer County, New Jersey

Summary

The QA Compliance Specialist is responsible for overseeing vendor and material qualification processes, ensuring compliance with regulatory standards, and supporting inspection readiness activities within a regulated manufacturing environment.

Responsibilities
  • Oversee the qualification of new vendors and materials, ensuring adherence to established procedures and regulatory requirements.
  • Maintain and update the Approved Vendor List, ensuring accuracy and compliance with site standards.
  • Track and complete periodic vendor reassessments to support ongoing compliance and supplier lifecycle management.
  • Manage documentation, schedules, and follow-ups related to vendor and material qualification, including change controls and supplier notifications.
  • Ensure all materials used in manufacturing have required BSE/TSE evaluations and initiate site documentation for supplier changes as needed.
  • Collaborate with internal and external quality teams, legal, and vendors to generate and route Quality Assurance Agreements and support vendor audits.
  • Provide support for inspection readiness, including preparation for regulatory inspections and participation in audit activities.
  • Continuously review and improve vendor management and qualification processes to enhance compliance and support day-to-day business needs.
Qualifications
  • Bachelor’s degree in Life Sciences, Chemistry, Biology, Engineering, Quality Assurance, Regulatory Affairs, or a related discipline, with at least two years of relevant experience.
  • Equivalent combination of education and relevant experience in a regulated pharmaceutical, biotechnology, or manufacturing environment may be considered.
  • Experience in Quality Assurance, Quality Compliance, Vendor Quality, Supplier Quality, or a related regulated environment.
  • Knowledge of vendor and material qualification, supplier change management, quality agreements, and change control processes.
  • Familiarity with inspection readiness activities and regulatory inspection support.
  • Strong skills in cross-functional collaboration, documentation, organization, and communication.
  • Ability to manage multiple priorities and support business needs in a fast-paced, regulated environment.
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