Associate Principal Quality Partner, Shop Floor

AbbVie

Quick summary

Work type
On-site
Location
Branchburg, NJ
Posted
8 days ago
Closes
Jun 19, 2126
Nearby
99+ roles within 25 mi

Market check

Salary context

How this pay compares to similar roles

Similar $172k
$127k most similar roles pay here $217k

This listing doesn't post a salary. Most similar roles pay $136,075–$208,353.

Based on 239 similar postings.

Employer

About AbbVie

AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines and solutions in immunology, oncology, neuroscience, and eye care. Its products include Humira, Skyrizi, and Rinvoq.

AbbVie currently has 36 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 5 roles with salary data.

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At a glance

TL;DR · Associate Principal Quality Partner, Shop Floor

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The Associate Principal Quality Partner role at AbbVie in Branchburg, NJ, involves providing senior-level quality oversight and leadership within Operations. This position focuses on ensuring compliance with cGMP requirements and regulatory standards while driving continuous improvement initiatives. Day-to-day responsibilities include conducting impact assessments for nonconformances, approving SOPs and NCRs, and leading corrective action strategies. The role requires strong communication skills and experience in pharmaceutical or biologics manufacturing environments. Candidates should have a background in physical sciences, pharmacy, engineering, or a related field, along with at least 8 years of combined experience in Manufacturing, QA, R&D. Familiarity with electronic document management systems and quality governance is preferred, as well as the ability to influence cross-functional teams and lead strategic initiatives.

Skills

cGMP GxP ISO standards Quality Management Systems Electronic Document Management Systems Lab Information Management Systems Root Cause Analysis Risk Assessment Corrective and Preventive Action (CAPA) Compliance Oversight Cross-Functional Leadership Quality Issue Resolution Audit Readiness Regulatory Compliance

What you'll do

  • Provide strategic quality oversight for critical phases of Operations and Manufacturing.
  • Complete impact assessments for nonconformances with robust risk evaluation.
  • Act as senior QA approver for SOPs, compliance records, NCRs, CAPA plans.
  • Lead site projects and compliance initiatives to embed quality requirements early.
  • Partner with leadership to identify systemic risks and influence corrective actions.
  • Ensure documentation is complete, accurate, compliant, and aligned with procedures.
  • Provide senior-level support for quality incident investigations and root cause analysis.

What we're looking for

  • Bachelor’s Degree in Physical or Life Sciences, Pharmacy, or Engineering required.
  • 8+ years of combined experience in Manufacturing, QA, R&D in pharmaceutical/biologics industry.
  • Deep GxP/cGMP quality assurance experience on shop floor with focus on issue resolution and governance.
  • Strong communication skills, both oral and written.
  • Experience supporting quality issue resolution, compliance oversight, and cross-functional leadership.

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