Qc Associate

4 semanas atrás

Lisboa, Lisboa, Portugal Hovione Tempo inteiro

.Join a Market LeaderHovione 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 life.You will be responsible to:Define and implement quality control techniques to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements.Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.Rigorously manage, execute and support all assigned projects in accordance with applicable GMP, quality operational standards/procedures and legal regulations, escalating as appropriate.Guide less experienced colleagues in undertaking assigned project tasks.Propose new methodologies considering project demands and requirements.Execute project-specific analytical tasks and act as a stakeholder liaison.Provide an example of professionalism and lead the induction and training of new colleagues within the area.Ensure that all analytical tasks, including method development, method creation, method transfer, method validation, protocol preparation, and report preparation, are well managed and delivered on time, safely, efficiently, reliably, and cost-effectively.Solve analytical problems relating to assigned projects by providing collaborative and timely support to all areas and departments.Ensure effective and proactive flow of information between the Analytical team and internal/external stakeholders.Review work generated by the team ensuring all procedures are followed.Create, investigate, and evaluate CAPAs, incidents, and deviations.Perform equipment maintenance, internal calibrations, and internal qualifications on designated laboratory instruments.Accurately use and maintain all laboratory information systems.Maintain good hygiene and housekeeping within the laboratory.Maintain all laboratory records, project and general logbooks and notebooks to an acceptable GLP standard.Fulfill and promote all applicable GMP requirements and HSE regulations.Be a leading advocate for safe operating and high-quality performance

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