. Analyses and measures the effectiveness of existing business processes within own domain. Participates in design and implementation of re-engineering ...
Participate in the Process Validation (PV) and Process Robustness activities mainly on secondary manufacturing processes (i.e. immunostimulants, adsorption, ...
We are looking for a validation supervisor for Quality Improvement Plans for a pharmaceutical partner in Walloon Brabant.. Writing documentation for ...
• Participates in internal audits and inspections as well as in conducting follow-up to non-compliance issues.• Audits/inspections may include cGLP, ...
Vérifier la concordance entre les Critical Data d'un dossier d'enregistrement régulatoire et les documents utilisés dans les activités opérationnelles ...
Role purpose• Ensure energy excellence for the Belgian Borealis locations.• Responsible for the local implementation of the group wide strategy for ...
• Support manufacturing of clinical batches, stability batches and process validation batcheso Technical writing: protocols, reports, SOPs, manufacturing ...