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Pharmeng • Helsinki, Uusimaa, Finland
Role & seniority: Quality Assurance Consultant; mid-level to senior QA professional
Stack/tools: GxP regulations; Quality Management System (QMS); Quality Manual; Site Master File; CAPA; deviation/change control; audits (internal/external/self-inspections); local product release (QP); GDP for warehousing/distribution; Training Management System (LMS)
Implement, maintain, and oversee the QMS at local affiliates; manage quality risk, complaints, deviations, CAPA, and inspections
Lead local complaint coordination, change control assessment, deviation management, self- and authority inspections, and GxP surveillance
Oversee local product release, GDP compliance for warehousing/distribution, training management, and supplier quality activities
Bachelor’s in Quality Management, Life Sciences, or related field
≥5 years QA experience in pharmaceutical/healthcare
Strong GxP knowledge; analytical and problem-solving abilities
Excellent communication; ability to work independently and in teams
Proficiency with QMS and LMS
Experience with GDP, supplier qualification and audits, recalls, and local repackaging/relabeling
Training program design/management and CAPA closure processes
Location & work type: Local affiliates (global scope); work type not specified in provided information
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.