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Pharmeng • Złoty Stok, Lower Silesian Voivodeship, Poland
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 regulations and quality standards; QA systems for CAPA, change control, deviations, audits, recalls, and supplier management.
Implement, maintain, and oversee the local QMS and related quality governance (QMS, Quality Manual, Site Master File).
Lead quality risk management, CAPA, deviations, changes, inspections, and self-audits; manage complaints and product recalls.
Oversee local product release (local QP), GDP for warehousing/distribution, supplier qualification/audits, and training oversight.
Bachelor’s degree in Quality Management, Life Sciences, or related field.
5+ years of QA experience in pharma/healthcare; strong GxP knowledge.
Analytical problem-solving, effective communication, and ability to work independently and in teams.
Proficiency with QMS and LMS; strong organizational and time-management skills.
Experience with audits (internal/external), CAPA closure, supplier quality management, and recalls.
Leadership/coordination skills for cross-functional teams; experience with repackaging/relabeling activities.
Location & work type: Local affiliates (on-site); full-time position.
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.