... manufacturing of recombinant protein Active Pharmaceutical Ingredients (API) according to pre approved SOPs. Perform routine cell culture activities. Assist where required in the commissioning, validation and re-validation of equipment. Maintain cGxP ...
... manufacturing of recombinant protein Active Pharmaceutical Ingredients (API) according to pre approved SOPs. Perform routine cell culture activities. Assist where required in the commissioning, validation and re-validation of equipment. Maintain cGxP ...
... Analytics, Engineering, Quality, Technical Transfer, Validation, Research & Development and Regulatory Affairs. ... in Process Engineering within a pharmaceutical manufacturing operation or in a pharmaceutical operationFunctional knowledge of cGMPs and ...
... Analytics, Engineering, Quality, Technical Transfer, Validation, Research & Development and Regulatory Affairs. ... in Process Engineering within a pharmaceutical manufacturing operation or in a pharmaceutical operationFunctional knowledge of cGMPs and ...
... Analytics, Engineering, Quality, Technical Transfer, Validation, Research & Development and Regulatory Affairs. ... in Process Engineering within a pharmaceutical manufacturing operation or in a pharmaceutical operationFunctional knowledge of cGMPs and ...
... applicable to secondary manufacturingKnowledge of validation technology, production and management processes within and external to the pharmaceutical industryHow to applyApply now for ...
... manufacturing of recombinant protein Active Pharmaceutical Ingredients (API) according to pre approved SOPs.Perform routine cell culture activities.Assist where required in the commissioning, validation and re-validation of equipment.Maintain cGxP ...
... evaluation of submissions to the Pharmaceutical Benefits Advisory Committee (PBAC) requesting listing of pharmaceuticals on the Pharmaceutical Benefits Scheme (PBS), as well ...
... in leading changes Knowledge of validation technology, production and management processes within and external to the pharmaceutical industry Demonstrated understanding of cGMP, ...
... initial development through validation Experience in recipe and workflow authoring and experience configuring master data and equipment in MES Experience in process automation, MES and batch manufacturing industry standards Pharmaceutical experience and a ...