AbdiBio Quality Systems Engineer

Abdi İbrahim, founded in 1912, has the largest product portfolio in the sector and is the largest employer in the Turkish pharmaceutical industry with 5.500 employees. Abdi İbrahim has been the leader of Turkey’s pharmaceutical industry since 2002 with its powerful vision.Today, Abdi İbrahim operates in 17 countries outside Türkiye, exports to more than 70 countries ranging from Canada to European Union member states, from North Africa to Asia. As a corporate citizen working towards creating a better world and a better future, adhering to its mission in the sector and to the requirements of societal priorities, Abdi İbrahim focuses on sustainability in all its business processes. Its vision for 2025 - apart from maintaining its status as a wholly local company - is to become "one of the top 100 pharmaceutical companies in the world.We are looking for Quality Systems Engineer to join our Fill&Finish Team in Biotechnological Products Production Facility (AbdiBio) at Esenyurt campus.The requirements for the successful candidate are:Bachelor’s degree in Bioengineering , Chemical Engineering, Chemistry or Pharmacy.Knowledge of technical document writing within a GMP manufacturing facility.Knowledge of basic manufacturing operation related to Warehouse, Fill Finish and Packaging.Preferably with working experience in GMP Manufacturing Facility.Multitasking on quality management system documentation to ensure adherence of schedule.Preparation of Standard Operating Procedures, instructions logbook, and batch records, validation protocols effectively and competently.Strong problem-solving and analysis capabilitiesAbility to comprehend and converse in English to communicate effectively.The key duties of the successful candidate are:Planning and realization of Dispensing, Filling and packing within the scope of commercial production of products, coordination of the team and control of prepared documents.Involving in qualification activities by preparing document and executing activities.Working on continuous improvement programme for operational efficiency and better compliance.Coordinating with other departments for manufacturing activitiesResponsible of Quality management system such as Change control, Deviation, CAPA etc.Preparation of Equipment URSs related to Dispensing, Fill Finish and Packaging department.Preparation and control of the SOPs and Batch records of all steps of the production process.Working, ensuring and controlling to be worked in compliance with GMP and GLP rules.Provides data security for the preparation and storage of all data related to production, to develop the existing method.Responsible for data management and data integrity issues and ensures the continuity of systems in accordance with data integrity.Applicants with suitable qualifications are kindly invited to apply through LinkedIn. All applications will be acknowledged and treated confidentially.Candidates who will be invited to job interviews will be contacted primarily via phone.