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Pharmeng • Brussels, Brussels-Capital, Belgium
Role & seniority: Senior Quality Assurance Consultant (QA/Quality Management focus) with 5+ years in QA within pharma/healthcare.
Stack/tools: Quality Management System (QMS); Learning Management System (LMS); GxP regulatory framework; QA documentation (Quality Manual, Site Master File); GDP/LMD requirements; CAPA/Change Control/Deviation systems.
Lead QMS implementation, maintenance, and oversight at local affiliates; manage local quality manual, site master file, and GxP surveillance.
Oversee quality risk management, CAPA from deviations/audits/self-inspections, and manage complaints, change control, deviations, product recalls, and recalls/return processes.
Manage local product release (local QP), inspections, supplier quality activities, training programs, and GDP compliance for warehousing/distribution.
5+ years in Quality Assurance in pharma/healthcare
Strong knowledge of GxP regulations and quality standards
Analytical/problem-solving, and clear communication
Ability to work independently and with teams
Proficiency with QMS and LMS
Experience with GDP, supplier quality audits, and recall management
Leadership/people management capabilities
Experience with audit planning, CAPA closure, and change-control processes
Location: Local affiliates (onsite)
Work type: Full-time (onsite with possible travel for inspections/audits)
Job Summary: The Quality Assurance Consultant is responsible for the implementation, maintenance, and oversight of the Quality Management System (QMS) in local affiliates. This role ensures compliance with regulatory requirements, quality standards, and company policies. The Quality Assurance Consultant will manage quality risk, complaints, change controls, deviations, CAPA, authority inspections, self-inspections, GxP surveillance, product quality reviews, training, local product release, and oversight of GDP requirements for local warehousing and distribution.