to assist their experienced regulatory affairs pharmacist team. You need at least TWO full years of regulatory at a similar level to a pharmacist. Assist the regulatory affairs pharmacist team with all aspects of
advantageous
Significant experience of regulatory drug development, manufacture, commercialisation or equivalent
/>Knowledge of regulatory procedures and legislation for drug development, product registration, line extension
/>Knowledge of regulatory procedures and legislation for drug development, product registration, line extension
advantageous Significant experience of regulatory drug development, manufacture, commercialisation or equivalent Knowledge of regulatory procedures and legislation for drug development, product registration, line extension Knowledge of regulatory procedures and legislation for drug development, product registration, line extension
advantageous Significant experience of regulatory drug development, manufacture, commercialisation or equivalent Knowledge of regulatory procedures and legislation for drug development, product registration, line extension Knowledge of regulatory procedures and legislation for drug development, product registration, line extension
advantageous Significant experience of regulatory drug development, manufacture, commercialisation or equivalent Knowledge of regulatory procedures and legislation for drug development, product registration, line extension Knowledge of regulatory procedures and legislation for drug development, product registration, line extension
advantageous Significant experience of regulatory drug development, manufacture, commercialisation or equivalent Knowledge of regulatory procedures and legislation for drug development, product registration, line extension Knowledge of regulatory procedures and legislation for drug development, product registration, line extension
for aggregate reports while undertaking a local review and ensure the submission of Periodic Safety Update for MAH, Support in the review of new/revised safety regulations (for drugs non-medicinal products & LSO/CSTL with CAPA implementation, procedural document review from Subject Matter Experts and Area leads - depending familiarity with industry principles of product vigilance, drug development and pharmacology proficiency in Medical
for aggregate reports while undertaking a local review and ensure the submission of Periodic Safety Update for MAH, Support in the review of new/revised safety regulations (for drugs non-medicinal products & LSO/CSTL with CAPA implementation, procedural document review from Subject Matter Experts and Area leads - depending familiarity with industry principles of product vigilance, drug development and pharmacology proficiency in Medical
to support and assist the Regulatory Affairs pharmacists with the day-to-day administrative RA tasks.
to support and assist the Regulatory Affairs pharmacists with the day-to-day administrative RA tasks.