Hovione
Sara Martins has an extensive background in pharmaceutical quality control and validation. Sara has experience working as a Quality Control Manager at Hovione, where Sara oversees teams responsible for analytical method validations and regulatory support for various pharmaceutical products. Sara has also held roles as a Validation Team Leader and Analytical Chemist. Sara's educational background includes a Postgraduate degree in Biopharmaceutical Sciences and a MSc in PharmD Pharmaceutical Sciences. Prior to their current role, Sara gained experience as a QC Trainee and Pharmacist Trainee at different pharmaceutical companies.
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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.