Hovione
Ana Rita Pereira is a Senior QC Technical Specialist with extensive experience in quality control within the pharmaceutical industry. Ana Rita has held various leadership positions, overseeing teams responsible for the validation of analytical methods in process chemistry development and drug product development. Ana Rita also has experience as an Analytical Chemist, contributing to method validation and data review. Ana Rita's expertise includes QC improvement, developing procedures, coordinating training sessions, and ensuring compliance with cGMP standards.Ana Rita's dedication to high quality levels and continuous improvement is evident throughout their career.
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Hovione
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Hovione is an international company with over 60 years of experience in pharmaceutical development and manufacturing operations. As a Contract Development and Manufacturing Organization (CDMO) with a fully integrated offering of services for drug substances, drug product intermediates and drug products. The company has four FDA inspected sites in the USA, Portugal, Ireland and China and development laboratories in Lisbon, Portugal and New Jersey, USA. Hovione provides pharmaceutical customers services for the development and compliant manufacture of innovative drugs, including highly potent compounds, and customized product solutions across the entire drug life cycle. In the inhalation area, Hovione offers a complete range of services, from API, formulation development and devices. Hovione´s culture is based on innovation, quality and dependability. Hovione was the first Chemical/ Pharmaceutical Company to become a Certified B Corp, is a member of Rx-360, EFCG and participates actively in industry quality improvement initiatives to lead new global industry standards.