Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off-patent drugs to market.Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites.Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for lifeResponsibilities Performs qualitative and quantitative analyses of compounds, including drug substances, drug product intermediates and drug product. Recommends the analytical characterization package (Chemical, physical, performance) and controls the quality and accuracy of the data in compliance with legislation and regulatory standards of Quality, HSE and cGMP policies. Promotes the scientific excellence and innovation in the Analytical area and contributes with technical expertise to expand the Intellectual Property, product and technology portfolios.- Follow procedures with clear instructions- Work follows an established pattern, with a requirement to run standard procedures, analysis, reports or tests- Able to prioritize own work - Rigorously, accurately, efficiently and professionally execute and record all analysis activities in accordance with the applicable requirements and guidelines at RD analytical development laboratories, quality operational standards/procedures and legal regulations and following instructions received from ascending colleagues.- Testing may be required for the following (non-exhaustive) sample types; in-process control, intermediates, raw materials, new supplier samples, stability (informal) and finished products in an RD analytical development environment- Strive for Right First Time and Productivity in all assigned tasks- Be an advocate for safe operating and high-quality performance, alerting peers and ascending colleagues to any potential risks and suggesting optimizations or improvements- Develop and accumulate strong analytical technical expertise - Display professionalism and support the induction and training of new colleagues- Organize and define daily priorities within their assigned tasks to accurately and promptly perform the allocated sample analysis to meet the requirements of the periodic laboratory plan and areaKPIs- Adhere to the laboratory testing schedule in order to achieve an efficient process in the analytical laboratory- Take responsibility for all data individually generated and ensure it is in accordance with all applicable requirements and HSE regulations, adhering to all relevant Operating Procedures and industry standards in conducting all analytical activities- To maintain all checklists, laboratory records and notebooks in which he/she is involved to an acceptable standard and in accordance with Hovione internal procedures- Maintain good hygiene and housekeeping within the laboratory- Perform routine calibration, verification and applicable preventive/corrective maintenance of designated laboratory instruments- Issue notifications for maintenance/repair to qualified areas, requesting consumables whenever needed- Comply with the high standards in the R&D Analytical Development Laboratories- Bring any discrepancies, deviations or non-conformance in testing or work practice to the attention of the laboratory responsible or N+1 in accordance with Hovione internal procedures and to collaborate on finding solutions for such events- Report incidents and unexpected results and contribute to their investigation- Ensure appropriate communication with other internal department in relation to analytical work by using the appropriate Hovione processes.- Participate, as required, in the induction and training of new Analysts across Hovione- Seek out additional information when one feels that the available information is not enough- Follow all periodic performance review requirements, including completion of the self-assessment.- Maintain an open communication with colleagues, identifying and reporting any production, HSE, quality or other issues to management according to the required processes- Suggest and participate in improvements in the area in which the team member is assigned- Undertake any additional tasks to support the laboratory activities as and when required- Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health & safety rules/procedures, regulations and codes of practice.Qualifications- Qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related or other science-related field (mandatory)- Proven practical pharmaceutical or related industry experience in a QC laboratory or in a R&D analytical environment (mandatory)Hovione is a proud Equal Opportunity EmployerInclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.#J-18808-Ljbffr