Qualified Person (QP) – Konsultuppdrag
On-site · Stockholm, Stockholm, Sweden
Job Summary
Qualified Person (QP) for GMP-regulated pharmaceutical development and quality in a long-term, part-time consulting role south of Stockholm. You will be a key part of the quality organization, contributing QP expertise to GMP-regulated activities, collaborating with quality, analytical, and process development teams, supporting regulatory compliance, inspections/audits, deviation investigations, change controls and CAPA, and advising on quality and regulatory questions. The role offers flexibility in engagement model (self-employed or employed by SallyQ) and emphasizes a varied, knowledge-intensive environment with opportunities to contribute to quality systems and processes.
Required Qualifications
- QP-behörighet enligt EU:s läkemedelslagstiftning
- Flerårig erfarenhet från GMP-reglerad verksamhet
- Erfarenhet från läkemedelsutveckling, tillverkning eller kvalitetsarbete
- God förståelse för europeiska GMP-krav
- God kommunikationsförmåga på svenska och engelska
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