<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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Amino Chemicals

&lt;p&gt;&lt;strong&gt;A2W Pharma Limited&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;A2WPharma. is part of ABA Chemicals Corporation, Shanghai which provide custom manufacturing services to the pharmaceutical, biotechnological and agrochemical industries worldwide.&lt;/p&gt;
&lt;p&gt;A vacancy has arisen in the Quality Control Laboratory for the position of &lt;strong&gt;Quality Control Manager.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The ideal candidate should have a:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Degree in Chemistry, Pharmaceutical Sciences, Pharmacy, or a related scientific discipline.&lt;/li&gt;
&lt;li&gt;Minimum of 5 years&#039; experience in a pharmaceutical Quality Control laboratory, with at least 2 years in a supervisory or management role.&lt;/li&gt;
&lt;li&gt;Strong knowledge of EU GMP, ICH guidelines, and pharmacopoeial requirements.&lt;/li&gt;
&lt;li&gt;Experience with analytical techniques including HPLC, GC, UV, FTIR, and other laboratory instrumentation.&lt;/li&gt;
&lt;li&gt;Experience in OOS investigations, method validation, stability studies, and laboratory compliance&lt;/li&gt;
&lt;li&gt;Excellent leadership, organisational, and communication skills.&lt;/li&gt;
&lt;li&gt;Strong problem-solving abilities and attention to detail.&lt;/li&gt;
&lt;li&gt;Proficiency in laboratory software and Microsoft Office applications.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Main Tasks&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Reports to the QA Manager. Amongst other laboratory duties, the incumbent will be responsible to:&lt;/li&gt;
&lt;li&gt;Manage the day-to-day operations of the Quality Control laboratory.&lt;/li&gt;
&lt;li&gt;Ensure testing of raw materials, intermediates, packaging materials, and finished products is performed in accordance with approved specifications and GMP requirements.&lt;/li&gt;
&lt;li&gt;Review and approve laboratory data, analytical reports, specifications, protocols, and procedures.&lt;/li&gt;
&lt;li&gt;Oversee investigations relating to OOS, OOT, laboratory deviations, and CAPAs.&lt;/li&gt;
&lt;li&gt;Ensure laboratory equipment is qualified, calibrated, and maintained.&lt;/li&gt;
&lt;li&gt;Manage stability studies and environmental monitoring programmes where applicable.&lt;/li&gt;
&lt;li&gt;Coordinate method validation, verification, and analytical method transfers.&lt;/li&gt;
&lt;li&gt;Collaborate closely with Quality Assurance, Production, R&amp;amp;D, and Supply Chain departments. We are offering a full time position, with an attractive remuneration package for this position along with training and opportunities for professional growth.&lt;/li&gt;
&lt;/ul&gt;

Quality Control Manager

&lt;p&gt;&lt;strong&gt;Corporate Technical Services Manager&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Company: A2W Pharma Ltd&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;A2W Pharma Ltd is seeking to recruit a highly motivated and experienced Corporate Technical Services Manager to join our growing team.&lt;/p&gt;
&lt;p&gt;The successful candidate will be responsible for leading and coordinating the Company&#039;s Technical Services function, ensuring the efficient management of manufacturing processes, technology transfer activities, validation programmes, process optimisation, investigations, and continuous improvement initiatives, while maintaining full compliance with GMP requirements.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead and manage the Technical Services Department.&lt;/li&gt;
&lt;li&gt;Coordinate technology transfer projects from development through to commercial manufacturing.&lt;/li&gt;
&lt;li&gt;Oversee process validation, cleaning validation, equipment qualification and continued process verification activities.&lt;/li&gt;
&lt;li&gt;Provide technical support to Production, Engineering, Quality Assurance and other cross-functional departments.&lt;/li&gt;
&lt;li&gt;Lead investigations related to manufacturing processes, deviations, CAPAs and change controls.&lt;/li&gt;
&lt;li&gt;Identify and implement process improvements to enhance efficiency, quality and productivity.&lt;/li&gt;
&lt;li&gt;Prepare, review and approve technical documentation, protocols and reports.&lt;/li&gt;
&lt;li&gt;Support regulatory inspections, customer audits and internal audits.&lt;/li&gt;
&lt;li&gt;Ensure compliance with EU GMP guidelines, company procedures and applicable regulatory requirements.&lt;/li&gt;
&lt;li&gt;Manage departmental objectives, budgets and resource planning.&lt;/li&gt;
&lt;li&gt;Coach, mentor and develop members of the Technical Services team.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Requirements&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Degree in Chemical or Mechanical Engineering, Chemistry, or another related scientific discipline.&lt;/li&gt;
&lt;li&gt;Minimum of 5 years&#039;s experience within the pharmaceutical manufacturing industry, including experience in Technical Services or Process Engineering.&lt;/li&gt;
&lt;li&gt;Strong knowledge of EU GMP requirements and pharmaceutical manufacturing processes.&lt;/li&gt;
&lt;li&gt;Experience in process validation, technology transfer and continuous improvement projects.&lt;/li&gt;
&lt;li&gt;Excellent leadership, communication and organisational skills.&lt;/li&gt;
&lt;li&gt;Strong analytical and problem-solving abilities.&lt;/li&gt;
&lt;li&gt;Ability to work independently and collaboratively within a multidisciplinary environment.&lt;/li&gt;
&lt;li&gt;Excellent command of the English language, both written and spoken.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We Offer&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;An opportunity to join a dynamic and growing pharmaceutical company.&lt;/li&gt;
&lt;li&gt;A challenging role with opportunities for professional development.&lt;/li&gt;
&lt;li&gt;A competitive remuneration package commensurate with experience and qualifications.&lt;/li&gt;
&lt;li&gt;Health Insurance upon successful completion of the probation period.&lt;/li&gt;
&lt;li&gt;Other company benefits in line with company policies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;How to Apply&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Interested candidates are invited to send their CV and a covering letter. Applications will be treated in the strictest confidence.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Only shortlisted candidates will be contacted.&lt;/p&gt;

Corporate Technical Services Manager

&lt;p&gt;Amino Chemicals Ltd. is part of Aba Chemicals Corporation, Shanghai who provides custom manufacturing services to the pharmaceutical, biotechnological and agrochemical&lt;/p&gt;
&lt;p&gt;industries worldwide. Amino Chemicals is an Active Pharmaceutical Ingredients manufacturer that has been developing innovative and proprietary processes since 1993.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;Due to the expansion of our operations, we require for immediate employment A &lt;strong&gt;HEALTH, SAFETY, SECURITY &amp;amp; ENVIRONMENTAL (HSSE) OFFICER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Purpose:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The ideal candidate will be assisting the HSE Manager in participating in the implementation of a companywide HSE management system in line with standard requirements, corporate guidelines and local regulations with the aim of achieving the company HSE objectives.&lt;/p&gt;
&lt;p&gt;Among other tasks, this role involves:&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;a. Auditing and Inspections&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Conduct regular HSE inspections across operational areas.&lt;/li&gt;
&lt;li&gt;Audit compliance with company policies, local regulations, and international standards (ISO 14001, ISO 45001).&lt;/li&gt;
&lt;li&gt;Identify hazards, unsafe practices, or environmental risks and recommend corrective actions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;b. Incident Reporting and Investigations&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Document all HSE incidents, near misses, and accidents.&lt;/li&gt;
&lt;li&gt;Lead investigations to determine root causes.&lt;/li&gt;
&lt;li&gt;Prepare reports with findings, lessons learned, and preventive measures.&lt;/li&gt;
&lt;li&gt;Follow up on implementation of corrective and preventive actions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;c. Risk Assessments&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Conduct risk assessments for operations, equipment, and chemical handling.&lt;/li&gt;
&lt;li&gt;Identify potential hazards and implement control measures.&lt;/li&gt;
&lt;li&gt;Maintain and periodically update risk assessment records.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;d. Environmental&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Monitor environmental aspects such as waste, water, emissions, and resource use.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;e. Occupational Hygiene&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Monitor workplace conditions to protect employee health (chemical exposure, noise, dust, etc.).&lt;/li&gt;
&lt;li&gt;Implement health surveillance programs.&lt;/li&gt;
&lt;li&gt;Recommend engineering controls or PPE to reduce risks.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;f. H&amp;amp;S Training&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Plan and conduct health and safety training for staff and contractors.&lt;/li&gt;
&lt;li&gt;Promote safe work practices, emergency procedures, and proper use of PPE.&lt;/li&gt;
&lt;li&gt;Raise awareness to foster a strong safety culture.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;g. Security Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Monitor and enforce site security protocols and access control procedures.&lt;/li&gt;
&lt;li&gt;Liaising with the security on duty and be the point of reference between our company and the security contractor&lt;/li&gt;
&lt;li&gt;Issuing of card access passes&lt;/li&gt;
&lt;li&gt;And any other security issues&lt;/li&gt;
&lt;/ul&gt;
&lt;p&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;Hold an MQF Level 6 (bachelor’s degree in safety or related fields)&lt;/li&gt;
&lt;li&gt;Experience: Minimum 3 years of work experience in Health &amp;amp; Safety, preferably in industrial or pharmaceutical environments.&lt;/li&gt;
&lt;li&gt;A sound scientific background with a minimum ‘A’ Level Chemistry&lt;/li&gt;
&lt;li&gt;Fluency in English&lt;/li&gt;
&lt;li&gt;Ability to conduct audits, risk assessments, and incident investigations&lt;/li&gt;
&lt;li&gt;Strong knowledge of occupational health, safety, environmental regulations,&lt;/li&gt;
&lt;li&gt;Knowledge of ISO14001 and ISO 45001International Standards&lt;/li&gt;
&lt;li&gt;Be fluent in the use of Microsoft Office Applications&lt;/li&gt;
&lt;/ul&gt;