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Pharmeng • Stockholm, Sweden
Role & seniority: Quality Assurance Consultant; mid-to-senior level with 5+ years QA experience in pharma/healthcare
Stack/tools: Quality Management System (QMS); Learning Management System (LMS); GxP regulatory framework; QA processes (CAPA, change control, deviations, complaints, recalls, audits)
Implement, maintain, and oversee the local QMS and related quality records (Quality Manual, Site Master File)
Manage quality risk, complaints, deviations, CAPA, inspections, self-inspections, and local product release
Oversee GDP for local warehousing/distribution, supplier quality, recalls, and return/destruction activities
Bachelor’s degree in Quality Management, Life Sciences, or related field
5+ years QA experience in pharmaceutical/healthcare
Strong GxP knowledge; analytical, problem-solving, and communication skills
Proficiency with QMS and LMS; ability to work independently and cross-functionally
Experience with audits (internal/external), supplier qualification, and CAPA closure
Repackaging/relabeling change management; product recalls and return workflows
Leadership or coordination of cross-site quality activities
Location & work type: Location not specified; work type likely full-time and local-affiliate oriented (global scope).
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.