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Blackbull International
GMP, regulatory submissions, production validation – in pharma, documentation and compliance matter as much as the product itself. We source interim managers who are at home in this environment.
Head of Quality, Qualified Person, Head of Regulatory Affairs, production management, Head of Supply Chain and project leads for site qualifications. Profiles in our network bring experience from pharma manufacturers, CMOs and biotech companies.
Production validation, deviation management, CAPA, audit preparation – GMP is the foundation of pharmaceutical manufacturing. We source interim managers who have built quality systems and successfully guided companies through FDA and EMA inspections.
CTD dossiers, variations, renewals, national and centralised approval procedures – Regulatory Affairs demands precision and deadline discipline. Through our network, we find interim managers who have led approval processes for originator and generic products.
Sterile manufacturing, packaging, serialisation, supply chain security – pharma production is heavily regulated and capital-intensive. Our network includes interim managers who have run production sites and managed pharma supply chains.

Whether a vacancy, project or transformation – tell us what you need and we will find the right solution. Fast, confidential and free of charge.