Sobre o nosso cliente Our client is an international pharmaceutical company.
Descrição Plan, prepare and conduct external suppliers onsite audits for ensuring consistent high quality of the pharmaceutical goods and services to be purchased;Generate audit reports and approve Corrective and Preventive Actions plans provided by the suppliers;Ensure that critical findings observed during on-site audits are eliminated within a timely manner by performing a stringent follow-up of the respective CAPA;Perform paper-based and remote audits for less critical materials and services;Negotiate quality contracts with our suppliers and service providers;Participate in supplier monitoring and supplier management programs;Investigate and escalate supplier quality incidents;Participate in supplier relationship management initiatives and forums;Follow up, investigate, evaluate and close supplier quality complaints.Perfil ideal University degree, preferably in Chemistry, Pharmacy, or Engineering and have gained relevant practical experience in production or quality management;Experience in auditing of at least 2 of the following topics: Non-Sterile APIs, Excipients, Non-sterile Finished Drug Forms, Contract packaging organisations, Chemical substances, Medical Devices, Packaging Materials, Warehouses, Services;Knowledge of international authority regulations (e.g. PICs, ICH, and FDA) including applicable ISO norms;Structured, result-oriented work, reliability and discretion are just as important for you as high motivation, a self-assured manner, and excellent multi-cultural, negotiation and communication skills;These international tasks involve travelling (around 40%);Speak and write fluent English.Vantagens Excellent opportunity for your professional development.
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