<p>Situated on the island of Malta, just south of Italy in the Mediterranean Sea, Amino Chemicals was founded 1992, and became part of Dipharma Group in 1999. Following consecutive GMP audits by both FDA and MMA (EMA’s competent authority in Malta), it is focused on the chemical process development and industrialization of new generic APIs. Its facilities, comprising a 56 m3 multipurpose plant over an area of nearly 7,800 square meters was almost doubled in the recent years, as part of an expansion project which was started in late 2006, having been allocated a second industrial plot by the Malta Industrial Parks. This permitted the inauguration and commissioning of a second bulk solvent storage facility as well as the installation of a state of the art Nitrogen gas production plant. Furthermore, in March 2013, Amino Chemicals celebrated the inauguration of the new headquarters building, a modern space to welcome international customers and to offer to the employees a work environment which promotes innovation and team work. In June 2017, ABA Chemicals Corporation, a leading API and CMO producer in China with headquarters in Jiangsu, announced that it has completed the acquisition of Amino Chemicals, a very important first step for ABACHEM's international expansion. Through Amino Chemicals, ABA Chemicals intends to become a truly global company over the coming years.</p>

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&lt;p&gt;Amino Chemicals Ltd. is part of ABA Chemicals Corporation, Shanghai which provide custom manufacturing services to the pharmaceutical, biotechnological and agrochemical industries worldwide. Amino Chemicals is an Active Pharmaceutical Ingredients manufacturer that has been developing innovative and proprietary processes since 1993.&lt;br&gt;&lt;br&gt;&lt;strong&gt;A vacancy has arisen in the Quality Control Laboratory for the position of: &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;QC LABORATORY ANALYST&lt;/strong&gt;&lt;br&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The ideal candidate should:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Preferably have a first degree in Pharmacy, Chemistry and Biology&lt;/li&gt;
&lt;li&gt;Be fluent in English &lt;/li&gt;
&lt;li&gt;Experience in a similar environment and with at least 2 to 3 years’ experience.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Main Tasks&lt;/strong&gt;&lt;br&gt;Reports to the QC Manager. &lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Amongst other laboratory duties, the incumbent will be responsible for:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;analysing raw materials, intermediates, in-process, finished products and stability samples according to established methods and procedures&lt;/li&gt;
&lt;li&gt;preparing retention samples and to upkeep the relevant documentation&lt;/li&gt;
&lt;li&gt;carrying out routine calibration of laboratory instruments&lt;/li&gt;
&lt;li&gt;following and ensuring strict safety procedures and safety checks using analytical techniques and instrumentation, such as HPLC and GC interpreting data and adhering to strict guidelines on documentation when recording data.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;We are offering an attractive remuneration package for this position along with training and opportunities for professional growth.&lt;/strong&gt;&lt;/p&gt;

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