QA Officer

• Assist in developing, maintaining and updating the Animal care Quality Management System for medicines, medical devices, feed supplements and skin care products to comply with current regulations.
• To coordinate quality assurance activities relating to Animal care licensed veterinary medicinal products.

• Support in the development, maintenance and update of the corporate QMS;
• Audit: execute and follow-up of internal and external audits;
• Initiation and/or assessment of deviations and complaints;
• Initiation, assessment and management of change controls and CAPA plans;
• Plan, collaborate and check qualifications and validations;
• Writing management, quality related or technical reports;
• Perform and keep overview of quality-related tasks e.g. (mock)-recall, return goods/counterfeit product management, follow up of manufacturing activities, stability studies and Product Quality Reviews (PQRs), etc.
• Supervise the correct completion of work documents;
• To keep up to date the qualification/approval status of Ecuphar suppliers;
• To keep up to date the Ecuphar customers qualification for the proper distribution according the law;
• Plan, coordinate, perform and keep overview of the training of (new) employees;
• Transfer to sellable stock of product received from suppliers against respective Certificates of Analysis and approved packaging;
• To prepare and manage QTA’s (e.g. suppliers, distributors, warehouses, etc.);
• To attend audits performed by third parties or Health Authorities;
• To assure a Quality oversight of manufacturing, storage and transport activities;
• Perform work in accordance with regulation and permits;
• Support in budget control of expenses;
• Support in various operational issues customer service and supply chain

Have a good understanding of regulatory and GxP requirements. Propagate and defend the quality policy within the organisation.

• Good Technical Skills
• A logical and investigative mind
• A methodical approach to work
• Availability to travel for Audit purposes
• Interpersonal skills
• Writing and communication skills
• Quality and customer orientated

Minimum of 2 years pharmaceutical industry experience in area of Quality, Regulatory and operational GMP and/or GDP.