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Quality Systems Consultant

  • ... Posted on: Mar 12, 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 area We’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 activities Monitor and report quality metrics Partner cross‑functionally to strengthen compliance processes Required Background/Experience: 7+ years in QA/QMS within pharma, biotech, or medical device Strong knowledge of cGMP and FDA regulations Experience supporting or leading regulatory inspections Familiarity with QMS platforms (Veeva, TrackWise, or similar) Able to work independently in a fast‑paced environment #J-18808-Ljbffr

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Jobcon Logo Position Details

Posted:

Mar 12, 2026

Reference Number:

14660_770329E2071D23D5E38F04A412662E6A

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 area We’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 activities Monitor and report quality metrics Partner cross‑functionally to strengthen compliance processes Required Background/Experience: 7+ years in QA/QMS within pharma, biotech, or medical device Strong knowledge of cGMP and FDA regulations Experience supporting or leading regulatory inspections Familiarity with QMS platforms (Veeva, TrackWise, or similar) Able to work independently in a fast‑paced environment #J-18808-Ljbffr

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