A team of professionals for the production of medicinal products according to the latest technologies and international quality standards invites a LIMS quality engineer. Main duties and tasks:< /strong> data of ERP information systems (LIMS, 1C, SAP);Responsible for the introduction of new software modules and their harmonization with other modules used in the enterprise;Systematically analyze and provide appropriate reporting on the status of current tasks;Ensure the provision and maintenance 
 A team of professionals for the production of medicinal products according to the latest technologies and international quality standards invites a LIMS quality engineer.
 Main duties and tasks:< /strong>
 data of ERP information systems (LIMS, 1C, SAP);
Responsible for the introduction of new software modules and their harmonization with other modules used in the enterprise;Systematically analyze and provide appropriate reporting on the status of current tasks;Ensure the provision and maintenance of appropriate levels of software user access determined by the manager;Ensure synchronization of the software of various information systems; Develop and update work instructions for users in accordance with their access rights for working with the relevant software;Interact with other performers and structural units both by establishing systematic, effective verbal communication and by actively using business communication;< /li>Develop documentation within the framework of ensuring the functioning of analytical equipment;Work in electronic document management systems;Ensure proper circulation, storage and archiving of documentation according to your line of work. li> You can try yourself for this role if you have:
- Higher education (chemical , chemical-technological, biological, pharmaceutical, biotechnological);
 - Experience of working in the field of quality control at a pharmaceutical enterprise from 1 year is an advantage;
 - Experience of working with a laboratory information management system (LIMS ) is an advantage;
 - Knowledge of GMP/GLP, orientation in finding the necessary information on quality control (DFU/EP/USP);
 - Ability to analyze information and provide reasoned proposals for further actions; 
 - Understanding the main components and the principle of functioning of the pharmaceutical quality system;
 - A confident PC user (MS Office);
 - English at a level no lower than Intermediate
  
 We offer:
- Decent pay level and working conditions.
 - Guarantees according to KZpP of Ukraine.
 - Medical and accident insurance.
 - Corporate gym.
 - Opportunities for development and training.
 
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