<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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English

Amino Chemicals

&lt;p&gt;&lt;strong&gt;Roles and responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;- Manage the work of small documentation team&lt;/p&gt;
&lt;p&gt;- Set up priorities&lt;/p&gt;
&lt;p&gt;- Follow the effectiveness of the work of her/his team&lt;/p&gt;
&lt;p&gt;- Create new regulations (Standard Operation Procedure, Operative Instruction)&lt;/p&gt;
&lt;p&gt;- Keep up to date the in-force regulations (related to the department)&lt;/p&gt;
&lt;p&gt;- Create and update production batch records&lt;/p&gt;
&lt;p&gt;- Follow up the production program and keep the plan up-to-date&lt;/p&gt;
&lt;p&gt;- Manage Change Controls, Deviations and follow-up Corrective and Preventive Actions&lt;/p&gt;
&lt;p&gt;- To follow the production operations in the ERP system&lt;/p&gt;
&lt;p&gt;- Keep the databases up-to-date&lt;/p&gt;
&lt;p&gt;- Use MS Office in upper intermediate level (Outlook, Excel, Word)&lt;/p&gt;
&lt;p&gt;- Keep the contact with other departments as (Quality Assurance, Warehouse, Quality Control, R&amp;amp;amp;D)&lt;/p&gt;
&lt;p&gt;- Follow and report KPIs&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Experience and Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;- Bachelor Qualification in Industrial Engineering or similar (preferably in Chemical Engineering) with 5 years in similar position or at least 10 years in similar positions (preferably in chemical industry) &lt;/p&gt;
&lt;p&gt;- Experience in planning and understanding of production processes and principles&lt;/p&gt;
&lt;p&gt;- Familiar with ERP systems&lt;/p&gt;
&lt;p&gt;- Excellent communication and interpersonal skills&lt;/p&gt;
&lt;p&gt;- High attention to details and accuracy&lt;/p&gt;
&lt;p&gt;- Experience in risk analysis and investigations are considered an asset&lt;/p&gt;
&lt;p&gt;- Italian language knowledge is a strong advantage&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Competencies&lt;/strong&gt;:&lt;/p&gt;
&lt;p&gt;- Manage small group&lt;/p&gt;
&lt;p&gt;- Manage digital systems&lt;/p&gt;
&lt;p&gt;- Ability to work multi-tasking under time pressure&lt;/p&gt;
&lt;p&gt;- Analytical thinking and problem solving&lt;/p&gt;
&lt;p&gt;- Prioritization&lt;/p&gt;
&lt;p&gt;- Accuracy, attention to details&lt;/p&gt;
&lt;p&gt;- Drive for results&lt;/p&gt;
&lt;p&gt;- Quality orientation&lt;/p&gt;
&lt;p&gt;- Teamwork&lt;/p&gt;

Italian

Production Documentation Coordinator

&lt;p&gt;&lt;strong&gt;CORPORATE SENIOR MECHANICAL MAINTENANCE TECHNICIAN&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Technical Services Manager, the ideal candidate should preferably have&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A Maintenance or Mechanical Engineering background&lt;/li&gt;
&lt;li&gt;Conversant with standard mechanical workshop techniques and tools&lt;/li&gt;
&lt;li&gt;Minimum 5+ years experience in maintenance or related industries, ideally in a senior capacity&lt;/li&gt;
&lt;li&gt;Be fluent in English&lt;/li&gt;
&lt;li&gt;Be able to work on his/her own initiative and is pro-active whereby his/her recommendations&lt;/li&gt;
&lt;li&gt;Be able to work in a team, mentor junior technicians, and promote permanent solutions for continuous improvement&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;MAIN TASKS&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Routine Preventive Maintenance, Fault Finding and Repair on plant equipment including reactors, centrifuges, dryers, mills, micronizers and sievers.&lt;/li&gt;
&lt;li&gt;Maintenance of transfer pumps, pipelines, valves, vacuum pumps, and solvent tanks.&lt;/li&gt;
&lt;li&gt;Servicing of HVAC and chiller systems, cooling towers, boilers, scrubbers, air compressors and fire systems.&lt;/li&gt;
&lt;li&gt;Support of cleanroom facilities, water systems, and filtration equipment to required standards.&lt;/li&gt;
&lt;li&gt;Planning and conducting maintenance and servicing of plant, machinery and equipment to the required standards, including coordination of shutdowns and turnarounds.&lt;/li&gt;
&lt;li&gt;Support in the design, procurement, installation, and commissioning of new plant, machinery and equipment.&lt;/li&gt;
&lt;li&gt;Experience and knowledge of piping systems, rotating equipment, and pressure vessels is considered an asset.&lt;/li&gt;
&lt;li&gt;Experience in the pharmaceutical sector, FDF and/or API is considered a plus.&lt;/li&gt;
&lt;/ul&gt;

CORPORATE SENIOR MECHANICAL MAINTENANCE TECHNICIAN

&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;

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