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Pharmeng • Oslo, Norway
Role & seniority
Stack/tools
Quality Management Systems (QMS)
Learning Management Systems (LMS)
GxP regulatory framework (pharma/healthcare)
CAPA, deviations, change control, complaints, recalls
Audits (internal/external), self-inspections
Product quality review (PQR), supplier QA, GDP for warehousing/distribution
Top 3 responsibilities
Implement, maintain, and oversee the Quality Management System at local affiliates; manage local QMS documentation (Quality Manual, Site Master File)
Lead quality risk management, deviation/ CAPA processes, change control, complaints, inspections, and self-inspections
Oversee local product release, GDP compliance for warehousing/distribution, product recalls, supplier qualifications, audits, and QP responsibilities
Must-have skills
Bachelor’s degree in Quality Management, Life Sciences, or related field
≥5 years in Quality Assurance within pharma/healthcare
Strong knowledge of GxP regulations and quality standards
Analytical, problem-solving, and communication skills
Ability to work independently and collaboratively; proficient with QMS and LMS
Nice-to-haves
Leadership or team management experience
Regulatory inspection experience; experience with external audits and CAPA closure
Experience with repackaging/relabeling change management
Location & work type
Location: Local affiliates (global scope); specific site not stated
Work type: Not specified
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.