Sara Soroush Tiedemann +45 26116630
Sara Soroush Tiedemann +45 26116630

A specialized consulting partner for regulated life‑science industries.

Expert consultants who strengthen your pharma, biotech, and medical device operations and Projects.

Flexible engagement: projects, interim roles, or advisory support

Senior pharmaceutical leader with 20+ years of experience in GMP manufacturing (Drug Substance & Drug Product), Quality, and Aseptic Production across global organizations, including Novo Nordisk, Fujifilm Biotechnologies, Xellia Pharmaceuticals, and LEO Pharma.
Extensive international experience across diverse regulatory environments. Proven track record in building organizations, establishing manufacturing operations, enhancing quality systems, and preparing sites for inspections and commercial readiness.
Known for building high-performing teams, fostering cross-functional collaboration, and delivering robust, compliant processes that enable sustainable operational excellence.
Strategy & Business Development | Lead Auditor | Board Governance Certified.
+45 26116630,

Senior pharmaceutical engineering and quality professional with 20+ years of experience in GMP manufacturing, utilities, API production, sterile and non‑sterile operations, and large‑scale project environments across leading organizations including Novo Nordisk, Bavarian Nordic, Xellia Pharmaceuticals, LEO Pharma and NNE.
Extensive expertise in qualification & validation (FAT, SAT, IQ, OQ, PQ), quality leadership in technical projects, compliance oversight, change management, and driving risk‑based, practical solutions that support both production and engineering organizations. Recognized for strong cross‑functional collaboration, hands‑on problem solving, and implementing robust, compliant processes that withstand audits and inspections.
Quality Leadership | Qualification & Validation | GMP Compliance | Technical Projects | Risk & Change Management | Process Optimization.
+45 60469648,
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