Director Quality Assurance

Overview

A pharmaceutical company in Massachusetts is currently seeking an experienced professional to join their growing team as their new Associate Director, Quality Assurance Operations. In this role, the Associate Director, Quality Assurance Operations will be responsible for the Quality oversite for a manufacturing area (such as Drug Substance) as well as provide “on the floor” oversite of downstream purification manufacturing activities.

This is an onsite contract role in Bedford, MA

Responsibilities

• Provide on the floor quality operations support for all areas and own the master batch record lifecycle processes including final review and approval
• Provide technical quality guidance as part of teams conducting investigations for complex manufacturing events
• Review and approve complex deviations and / or Investigations that are site specific
• Actively support and / or lead preparation activities for pre-approval Inspections and / or responses to observations
• Work with product release teams to support issuance of drug substance Certificates of Conformance and any other disposition required activities.
• Manage CAPA records and may be required to function as a CAPA manager for minor or major CAPA as needed
• Serve as QA Reviewer or impact assessor for downstream purification change control records
• Support and / or review various reports from quality systems and ensure quality mindset is strong
• Own various Quality procedures and ensure the systems / processes are deployed effectively

Qualifications

Desired Skills

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