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Quality Consultant

  • Quality Consultant job type Posted on: Nov 02, 2026
  • Quality Consultant experience level JCW Group
  • Quality Consultant employment type Bridgewater, New Jersey
  • Quality Consultant employment type Onsite
  • Quality Consultant salary Full-time

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Job Title :

Quality Consultant

Job Type :

Full-Time

Job Location :

Bridgewater New Jersey United States

Remote :

No

Jobcon Logo Job Description :

Contract SOP Writer – Pharma Distribution & Logistics | Warren, NJ (Hybrid)I’m hiring a contract Quality Consultant for a global pharmaceutical company in Warren, NJ. They need US distribution procedures written and inspection-ready ahead of upcoming regulatory inspections.Details6-month contractStart ASAPHybrid: 3 days onsite in Warren, NJWhat you’ll doWrite US-market SOPs from scratch and adapt existing global versions. Topics include 3PL oversight, product release and disposition, cold chain temperature excursions, recall, deviation/CAPA/change control, and state licensing verification.Build process flow maps in Visio, Word, or Excel that link to each SOPRoute SOPs for Quality and Supply Chain approvalMaintain version control of hard and electronic copies so they are ready for inspectionWork with Logistics, Quality, IT, and Finance teamsWhat you need7+ years in pharma quality or supply chain. Medical device experience is also considered.Proven experience authoring SOPs yourselfKnowledge of pharma distribution and 3PL operationsStrong Word and Excel formatting skillsVeeva or other eDMS experience is a plus but not required

Jobcon Logo Position Details

Posted:

Nov 02, 2026

Reference Number:

10440_4482560264

Employment:

Full-time

City:

Bridgewater

Job Origin:

APPCAST_CPC

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Contract SOP Writer – Pharma Distribution & Logistics | Warren, NJ (Hybrid)I’m hiring a contract Quality Consultant for a global pharmaceutical company in Warren, NJ. They need US distribution procedures written and inspection-ready ahead of upcoming regulatory inspections.Details6-month contractStart ASAPHybrid: 3 days onsite in Warren, NJWhat you’ll doWrite US-market SOPs from scratch and adapt existing global versions. Topics include 3PL oversight, product release and disposition, cold chain temperature excursions, recall, deviation/CAPA/change control, and state licensing verification.Build process flow maps in Visio, Word, or Excel that link to each SOPRoute SOPs for Quality and Supply Chain approvalMaintain version control of hard and electronic copies so they are ready for inspectionWork with Logistics, Quality, IT, and Finance teamsWhat you need7+ years in pharma quality or supply chain. Medical device experience is also considered.Proven experience authoring SOPs yourselfKnowledge of pharma distribution and 3PL operationsStrong Word and Excel formatting skillsVeeva or other eDMS experience is a plus but not required

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