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Quality Systems Consultant

  • ... Posted on: Mar 08, 2026
  • ... JCW Group
  • ... Bridgewater, Vermont
  • ... Salary: Not Available
  • ... Full-time

Quality Systems Consultant   

Job Title :

Quality Systems Consultant

Job Type :

Full-time

Job Location :

Bridgewater Vermont United States

Remote :

No

Jobcon Logo Job Description :

Senior Manager, Quality Systems Compliance ( 6+ month Contract) — Hybrid | Bridgewater NJ areaWe’re supporting a life sciences client seeking a Senior Manager, Quality Systems Compliance to drive inspection readiness, internal audits, and QMS support. This is a hands-on contract role with strong visibility and impact.Key Responsibilities: Support FDA inspection readiness (BIMO and PAI)Contribute to internal audit program and remediation activitiesMonitor and report quality metricsProvide hands-on QMS support (CAPA, deviations, change control)Partner cross-functionally to strengthen compliance processesRequired Background/Experience: 7+ years in QA/QMS within pharma, biotech, or medical deviceStrong knowledge of cGMP and FDA regulationsExperience supporting or leading regulatory inspectionsFamiliarity with QMS platforms (Veeva, TrackWise, or similar)Able to work independently in a fast-paced environment

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Jobcon Logo Position Details

Posted:

Mar 08, 2026

Reference Number:

10440_4375277390

Employment:

Full-time

Salary:

Not Available

City:

Bridgewater

Job Origin:

APPCAST_CPC

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Senior Manager, Quality Systems Compliance ( 6+ month Contract) — Hybrid | Bridgewater NJ areaWe’re supporting a life sciences client seeking a Senior Manager, Quality Systems Compliance to drive inspection readiness, internal audits, and QMS support. This is a hands-on contract role with strong visibility and impact.Key Responsibilities: Support FDA inspection readiness (BIMO and PAI)Contribute to internal audit program and remediation activitiesMonitor and report quality metricsProvide hands-on QMS support (CAPA, deviations, change control)Partner cross-functionally to strengthen compliance processesRequired Background/Experience: 7+ years in QA/QMS within pharma, biotech, or medical deviceStrong knowledge of cGMP and FDA regulationsExperience supporting or leading regulatory inspectionsFamiliarity with QMS platforms (Veeva, TrackWise, or similar)Able to work independently in a fast-paced environment

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