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Pharmeng • Madrid, Community of Madrid, Spain
Role & seniority: Quality Assurance Consultant; mid-to-senior level with 5+ years QA experience in pharmaceutical/healthcare; capable of independent and collaborative work; leadership in QA processes.
Stack/tools: Quality Management System (QMS); Learning Management System (LMS); GxP/compliance frameworks; CAPA, change control, deviation, complaints, audits/inspections; GDP, local product release (QP), supplier audits, recalls, training management.
Lead QMS implementation, maintenance, and oversight for local affiliates (including Quality Manual and Site Master File).
Manage quality risk, deviations, CAPA, complaints, inspections (authority/self-inspections), and GxP surveillance.
Oversee local product release (QP), GDP-compliant warehousing/distribution, recalls, training, and supplier quality activities.
Bachelor’s degree in Quality Management, Life Sciences, or related field
5+ years QA experience in pharma/healthcare
Strong knowledge of GxP and quality standards
Analytical, problem-solving, and strong communication skills
Ability to work independently and in a team; proficient with QMS and LMS
Experience with GDP, local repackaging/relabeling, and recalls
Experience with supplier audits, CAPA lifecycle, and training program management
Location & work type: Location not specified; role appears to be full-time.
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.