🚀 Interim Quality Director

Hiring now — limited positions available!

Mantell Associates

💰 Earn $90.000 – $110.000 / year
  • 📍 Location: Torino
  • 📅 Posted: Oct 21, 2025

Mantell Associates is partnered with a well-established Pharmaceutical company, seeking an experienced Interim Quality Director to lead QA operations over an 18-month project.

This remote, full-time contract role starts mid-October, focusing on managing teams, ensuring GMP compliance, and working with contractors and vendors.

Interim Quality Director - Responsibilities

  • Lead and oversee the Quality Assurance department, managing in-house QA staff and external vendors/contractors to uphold GMP standards across manufacturing operations
  • Develop, review, and enforce quality systems, policies, and procedures to ensure product quality, regulatory compliance, and continuous improvement
  • Oversee deviation, non-conformance, CAPA, change control and quality assurance investigations; drive root cause analysis and ensure timely corrective and preventive actions
  • Conduct vendor qualification and oversight: assess contractor performance, audit suppliers and ensure contracted quality obligations are met
  • Manage audits and inspections readiness, including regulatory authority inspections, internal audits, and external audits, ensuring documentation is inspection-ready
  • Collaborate with cross-functional teams (Manufacturing, Regulatory, Supply Chain, Technical / Engineering) to align quality expectations and resolve quality-related issues impacting operations
  • Monitor quality metrics, performance KPIs, and report to senior leadership on QA status, risk areas, and compliance health

Interim Quality Director - Requirements

  • Extensive experience in pharmaceutical Quality Assurance within a GMP manufacturing environment
  • Previous leadership experience managing QA teams and working closely with external vendors and contractors
  • Proven track record of driving quality compliance and audit readiness in similar senior quality roles
  • Strong knowledge of European GMP regulatory frameworks; experience with Italian regulatory expectations is an advantage
  • Excellent communication, leadership, and stakeholder management skills; able to lead remotely and ensure high performance across geographies
  • Available to start mid-October; committed full-time (5 days / week) for the full 18-month contract duration

Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information on this opportunity, contact us at +44 (0) .

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