Manage, process and conduct investigations into product complaints and shipping incidents,Manage, process and conduct CAPA, supplier qualifications, and audits of GLP/GMP service providers.Provide guidance and training to staff regarding batch review/disposition process as well as other quality processes.Review and approve GMP production batch records for the release of clinical and/or commercialproducts.Facilitate the change control process, and oversee and manage change controls for changes made to development, validated and commercial products.Write SOPs for the creation, development or improvement of processes related to quality systems.Other essential duties as assigned.

- Designing the production of veterinary pharmaceutical drugs - Participation in Research and Development- Issuing of Quality Certifications- Management of Employees- Keeping contact with laboratories

- Participation in Research and Development- Issuing of Quality Certifications- Management of Employees- Keeping contact with laboratories- Designing the production of veterinary pharmaceutical drugs

- preparation of analytical samples- instrumental analysis of products (HPLC-MS)- preparative purification of products, development and elaboration of analytical methods- handling of analytical instruments- documentation

- sampling in practice- analytical preparation of the sample in practice- making analytical measurements with classical and with instrumental methods- getting acquainted with the usage of measuring instruments (HPLC,MS), evaluating the results- active participation in the planning, making and evaluation of analytic method-validation