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Pharmeng
Role & seniority: Quality Assurance Consultant (senior-level; 5+ years QA in pharma/healthcare)
Stack/tools: Quality Management System (QMS); GMP/GxP knowledge; Learning Management System (LMS); quality audits; CAPA; supplier qualification; GDP for warehousing/distribution; QA review of local product releases; PQR; deviation/change control processes
Implement, maintain, and oversee the local QMS, Quality Manual, Site Master File; manage QMS-related activities (risk, deviations, CAPA, audits, inspections)
Lead local quality risk management, complaint handling, change control assessment/closure, deviation management, CAPA generation, and inspection readiness
Oversee local product release (QP), GDP compliance for warehousing/distribution, supplier quality, training, recalls, and return/destruction processes
Strong knowledge of GxP regulations and quality standards
QA leadership, regulatory/compliance experience, audit and inspection management
Analytical, problem-solving, and communication skills; ability to work independently and cross-functionally
Proficiency with QMS and LMS
Experience with local repackaging/relabeling, transport/performance auditing, and recall management
Exposure to local warehousing, distribution quality controls, and GDP governance
Location & work type: Not specified in provided text; no explicit location or work-type details given.
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.