Do you have experience in the pharma or CRO industry supporting regulatory bioanalysis of small moleculesence ? contact me : charlotte.dhont@cx.ausy.be

• Experience in the pharma or CRO industry supporting regulatory bioanalysis of small molecules
• Knowledge of LC-MS based method for small molecule quantification
• Knowledge of the latest regulatory standards required for GXP studies including international guidance’s published by regulatory agencies such as FDA, EMA
• Previous experience managing contract research organizations

We offer an attractive salary with extra-legal advantages :

• Group insurance
• Hospitalisation insurance
• Meal vouchers of 7 euros gross per working day
• Reimbursement km or company car
• Monthly allowance (50 euros net per month)
• A 13th month
• Training
• Etc

A rate as freelance is also possible

Our client is a global biopharmaceutical company focusing on creating value for people living with neurology and immunology conditions.

• Interact with bioanalytical project representatives to execute the bioanalytical strategy, including method transfer/validation and bioanalysis (small molecule PK) at key strategic vendors.
• Assures bioanalytical tasks are executed with good scientific quality, within the adequate quality system, and within the agreed upon timelines.
• Collaborate with multiple internal and external stakeholders to execute the bioanalytical strategy
• Participate in clinical study design and documentation (lab manual, protocol, SAP,…)
• Participate in harmonization of bioanalytical testing and reporting processes