×
Register Here to Apply for Jobs or Post Jobs. X

Senior Quality Specialist

Job in Raritan, Somerset County, New Jersey, 08869, USA
Listing for: JobDiva, Inc.
Full Time position
Listed on 2026-10-03
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Engineering, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 110000 - 150000 USD Yearly USD 110000.00 150000.00 YEAR
Job Description & How to Apply Below

Summary :

We are seeking a Senior Quality Specialist with 10+ years of experience in Quality Assurance and Quality Systems within regulated environments. The ideal candidate will have strong expertise in GMP, supplier quality, external/contract manufacturing, CMO oversight, audits, CAPA, deviation management, risk assessment, and change control. This role will provide Quality oversight of suppliers and third-party manufacturers while ensuring compliance with applicable Quality Management Systems and regulatory requirements.

The candidate will collaborate closely with Supply Chain, Procurement, Manufacturing, Regulatory, and Quality teams to manage supplier performance, quality issues, audits, technical agreements, and continuous improvement initiatives.

Roles & Responsibilities :
  • Provide Quality oversight for External Manufacturing, Contract Manufacturing Organizations (CMOs), and third-party manufacturers to ensure compliance with GMP, Quality Agreements, and company quality standards.
  • Manage supplier qualification, approval, monitoring, and ongoing supplier performance through risk-based assessments, audits, quality metrics, and corrective actions.
  • Plan, coordinate, and execute supplier/CMO audits, including audit preparation, execution, reporting, observations, and CAPA follow-up to closure.
  • Lead and support deviation investigations, root cause analysis, CAPA development, implementation, and effectiveness checks.
  • Perform quality risk assessments related to suppliers, manufacturing processes, materials, changes, deviations, and quality events.
  • Develop, review, and maintain Technical Agreements, Quality Agreements, SOPs, specifications, and other GMP quality documentation.
Education & Experience:
  • Bachelor's degree in engineering, Life Sciences, Natural Sciences, or related field
  • 10+ years of Quality Assurance and/or Quality Systems experience in regulated environments
  • Experience supporting External Manufacturing and Contract Manufacturing Organizations (CMOs)
  • GMP/Good Manufacturing Practices expertise
  • Supplier Qualification and Supplier Management experience
  • Audit Planning, Execution, Reporting, and CAPA Follow-Up
  • Deviation Investigation and CAPA Management experience
  • Risk Assessment experience
  • Technical Agreements and Quality Documentation experience
  • Change Control Management experience
  • Strong cross-functional collaboration with Supply Chain, Procurement, and Manufacturing teams
  • Quality Systems experience (GMP, ISO, HACCP)
Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary