In chemicals, pharmaceuticals and life sciences, GMP-related processes, approval requirements and operational excellence are decisive for market success and security of supply. We fill critical roles discreetly and precisely — with a clear understanding of regulated environments, technical interfaces and the requirements of quality, safety and documentation.
- GMP / GxP / GDP: Good Manufacturing Practice / Good Practice / Good Distribution Practice
- Quality Assurance & Quality Control: QA / QC
- Regulatory Affairs & Marketing Authorisation: Regulatory Affairs, Authorisation
- Pharmacovigilance: PV
- Clinical Operations & Clinical Trials: Clinical Operations, Clinical Trials
- Validation & Cleanroom: Validation, CSV (Computerised System Validation), Cleanroom
- Occupational Health & Safety: EHS / HSE
- Hazardous Substances Management: REACH / CLP
Is a key position vacant, or do you need reliable short-term expertise in Quality, Regulatory Affairs or Operations? Get in touch with us — we identify and attract the right specialists and executives for your organisation.