<p>Aurobindo Pharma (Malta) Limited is a fully owned subsidiary of Aurobindo Pharma Pvt Ltd from Andhra Pradesh India, and is Asia’s largest generic pharmaceutical and API manufacturer, and among the major ‘vertically integrated’ pharmaceutical companies in India, exporting to over 125 countries across the globe.<br>Aurobindo Pharma (Malta) Limited is the gateway for Aurobindo’s pharmaceutical products in Europe. The Malta operations commenced in 2008 offering Analytical Services, Batch Release, Warehousing including Logistics at a pan European level.</p>

Aurobindo Pharma Malta

Relocation support

Visa assistance

Work permit costs

Professional training

Subsidized meals

Health insurance

Flexible working hours

Employee discounts

Wellness programs

&lt;p&gt;&lt;strong&gt;Objectives&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;· Ensure timely, effective and efficient day-to-day operation and management of the Quality Management System, in accordance with EU GMP and GDP and prevailing legislation, for assigned tasks.&lt;/p&gt;
&lt;p&gt;· Ensures regulatory compliance, data integrity and quality risk management principles are implemented and adhered to.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Tasks and Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;· Management of QMS documentation, inclusive of update and maintenance of such documents, their registers, and records arising from such documentation.&lt;/p&gt;
&lt;p&gt;· Participation in the self-inspection program, both as an auditor and as an auditee.&lt;/p&gt;
&lt;p&gt;· Receive and deliver training on specified GMP/Quality topics for Company personnel&lt;/p&gt;
&lt;p&gt;· Maintain the Company systems for handling personnel training and other administration matters for all Company employees.&lt;/p&gt;
&lt;p&gt;· Take part in the management of investigations, including those arising from complaints, inspections/audits, deviations, etc..&lt;/p&gt;
&lt;p&gt;· Review of a variety of periodical documents and reports received from third parties (e.g. product quality reviews, external audit reports, third party licenses, etc.).&lt;/p&gt;
&lt;p&gt;· Assist in the maintenance of the Company license, site master file and related policies.&lt;/p&gt;
&lt;p&gt;· Take part in continuous improvement initiatives, both within the scope of a team and individually.&lt;/p&gt;
&lt;p&gt;· Upkeep and maintenance of Quality Technical Agreements and ancillary documents.&lt;/p&gt;
&lt;p&gt;· Review and maintenance of (Item) Master Data in Oracle.&lt;/p&gt;
&lt;p&gt;· Verification and maintenance of suppliers/ customers certifications and licensing status, and maintenance of supplier audits and qualification system.&lt;/p&gt;
&lt;p&gt;· Review CAPA implementation to ensure all actions are satisfactory and effective.&lt;/p&gt;
&lt;p&gt;· Takes part in the change control program, including in the preparation, review and processing of internal change requests and those arising from suppliers and clients.&lt;/p&gt;
&lt;p&gt;· To liaise effectively with other departments to ensure assigned projects and exercises are conducted in a timely manner and in compliance with GMP.&lt;/p&gt;
&lt;p&gt;· Assists Company representatives during regulatory and customer audits.&lt;/p&gt;
&lt;p&gt;· Support the batch management process, Item master management process and ERP troubleshooting and activities in liaison with SC EU Eugia Subsidiary, EU Aurobindo Subsidiaries and Eugia Pharma Specialties&lt;/p&gt;
&lt;p&gt;· Carry out other duties as may reasonably be required.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;

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Maltese

EUGIA PHARMA MALTA - Quality Assurance Specialist

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