<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

Health insurance

Flexible working hours

Employee discounts

Wellness programs

&lt;p&gt;CuraTeQ Biologics (Malta) Ltd. is a fully owned subsidiary of CuraTeQ Biologics Pvt. Ltd., which, in turn, forms part of the Aurobindo Pharma Limited group of companies – one of the largest pharmaceutical families globally.&lt;/p&gt;
&lt;p&gt;CuraTeQ Biologics Pvt. Ltd. is a fully integrated biosimilar company which was founded in 2016 and headquartered in Hyderabad, Telangana, India. The company combines cutting-edge technology with robust manufacturing capabilities to deliver safe, effective and affordable biosimilars to patients worldwide. CuraTeQ Biologics (Malta) Ltd. acts as the European centralised Marketing Authorization Holder (MAH) for the biosimilar products manufactured at CuraTeQ Biologics Pvt. Ltd. The company currently holds 14 biosimilar programmes in the pipeline, and currently possesses 4 (four) Marketing Authorizations in the EU and UK, and aims to receive approvals for new biosimilar products in the coming years.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Job Descirption &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Follow company procedures to ensure the full traceability of all commercial transactions from sourcing to procurement, sales and invoicing.&lt;/li&gt;
&lt;li&gt;To remain impartial during all business transactions, thus protecting the best interest of the company at all times and to liaise with the Quality unit on all matters relating to purchasing of materials and services directly effecting quality.&lt;/li&gt;
&lt;li&gt;Ensuring that all goods acceptance of all incoming materials is in line with supporting documentations i.e.: Invoices/ Delivery Notes and/ or Packing lists.&lt;/li&gt;
&lt;li&gt;Goods receipt/export of all incoming materials on ERP systems and the generation of corresponding documentation.&lt;/li&gt;
&lt;li&gt;Generation of sales orders, purchase orders and invoices on ERP systems.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Requirments &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;3–4 years of relevant experience within a pharmaceutical environment or a similar industry.&lt;/li&gt;
&lt;li&gt;Good command of the English language, both written and verbal.&lt;/li&gt;
&lt;li&gt;Proficiency in Microsoft Windows and common Windows-based applications.&lt;/li&gt;
&lt;li&gt;Strong organisational and multitasking skills, with the ability to manage multiple priorities effectively.&lt;/li&gt;
&lt;li&gt;Ability to work independently, while also contributing effectively within a team environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;

English

Maltese

CuraTeQ Malta - Logistics Officer

Subsidized meals

&lt;h2&gt;About the job&lt;/h2&gt;
&lt;p&gt;&lt;strong&gt;Company Description&lt;/strong&gt; Aurobindo Pharma (Malta) Limited is a fully owned subsidiary of Aurobindo Pharma Pvt Ltd, Asia’s largest generic pharmaceutical and API manufacturer. As a key part of a major vertically integrated pharmaceutical group, the Malta entity serves as the gateway for Aurobindo’s pharmaceutical products in Europe, supporting exports to over 125 countries. Established in 2008, the Malta operations provide analytical services, batch release, warehousing, and pan-European logistics. Team members collaborate with international colleagues and support high-quality, affordable medicines for markets across Europe and beyond.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About the Role&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking an experienced Quality Assurance Specialist / Auditor to focus primarily on Quality Technical Agreements (QTAs) and GMP audits across suppliers, CMOs, and partners. The role will ensure agreements are maintained, audits are planned and followed up effectively, and key compliance risks are managed in line with EU GMP and internal quality requirements.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Quality Technical Agreements (QTA): Draft, review, negotiate, implement, and maintain QTAs with suppliers, CMOs, and partners, ensuring clear GMP responsibilities and compliance expectations.&lt;/li&gt;
&lt;li&gt;Audits: Plan, conduct, report, and follow up GMP audits of suppliers, CMOs, and service providers, including tracking observations through timely closure.&lt;/li&gt;
&lt;li&gt;Supplier/CMO oversight: Support supplier qualification, risk assessment, documentation review, and ongoing performance monitoring.&lt;/li&gt;
&lt;li&gt;QMS, documents, and EU guidance: Review and approve key quality documents, contribute to QMS activities as needed, and assess relevant EU GMP/EMA guideline updates for compliance impact.&lt;/li&gt;
&lt;li&gt;Cross-functional collaboration: Work with internal teams and affiliates to support quality and compliance objectives.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Strong Quality Assurance and Quality Management skills, including experience implementing and maintaining pharmaceutical quality systems.&lt;/li&gt;
&lt;li&gt;In-depth understanding of Good Manufacturing Practice (GMP) and EU regulatory guidelines relevant to medicinal products.&lt;/li&gt;
&lt;li&gt;Experience in Quality Auditing, including participation in or execution of internal and external audits.&lt;/li&gt;
&lt;li&gt;Bachelor’s degree (or equivalent) in Pharmacy, Chemistry, Life Sciences, or a related discipline; advanced qualifications are an asset.&lt;/li&gt;
&lt;li&gt;At least 5 years of experience in a GMP-regulated pharmaceutical environment, ideally within EU regulation.&lt;/li&gt;
&lt;li&gt;Strong analytical, problem-solving, and documentation skills, with attention to detail and a structured approach to quality-related tasks.&lt;/li&gt;
&lt;li&gt;Effective communication, negotiation and teamwork abilities, with proficiency in English.&lt;/li&gt;
&lt;/ul&gt;

EU Quality Assurance Specialist & Auditor

&lt;p&gt;We require a self-motivated individual who is dynamic, resilient and flexible. You also need to be a team player and possess the ability to work proactively and above all, have a ‘can do’ attitude and a commitment to learning and development.&lt;/p&gt;
&lt;p&gt;The Quality Engineering Coordinator forms part of the Engineering department is mainly responsible from the efficient planning of all laboratory equipment Qualifications and Maintenance in coordination with various service providers.&lt;/p&gt;
&lt;p&gt;Also, supporting the engineering team to maintain the laboratory equipment in a functional state.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The position requires:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Diploma in Science or Engineering&lt;/li&gt;
&lt;li&gt;Knowledge of lab equipment usage&lt;/li&gt;
&lt;li&gt;Preferably 2 years of laboratory experience&lt;/li&gt;
&lt;li&gt;Confidence in communicating in English (written and spoken)&lt;/li&gt;
&lt;li&gt;Good IT skills e.g. Microsoft Office (Word, Excel and Outlook)&lt;/li&gt;
&lt;/ul&gt;

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