Search the 14 jobs at Santen

Lead the strategy, planning, and execution of safety vigilance activities to ensure product quality and compliance. Responsible for risk management related to investigational and post-marketing products, including signal assessment, risk mitigation, and development of safety documents. Collaborate with cross-functional teams and contribute to R&D projects.

The Sales Representative at Santen is responsible for proposing sales targets, visiting customers for product promotion, overcoming sales objections, coordinating with team members on sales activities, and attending training and meetings related to their products.

The Senior Sales Executive at Santen develops and maintains relationships with healthcare professionals to achieve sales targets in both government and private sectors. The role involves actively promoting Santen products, collecting market insights, managing key accounts, and ensuring customer satisfaction while supporting marketing initiatives through various events.

The Manager, Market Access for the Iberia region will assess the local and regional market access landscape, develop strategic market access plans, support HTA submissions, manage pricing strategies, and build relationships with healthcare institutions to enhance access for Santen products.

The Marketing Administrative Assistant supports marketing and sales teams by coordinating marketing activities, managing travel arrangements, and providing administrative support. Responsibilities include documentation for project approvals, maintaining records, and ensuring compliance with regulations and policies.

The Senior Manager Global Pricing will implement global pricing strategies for therapeutic assets, overseeing pricing initiatives and collaborating with internal functions. Responsibilities include developing pricing frameworks, managing pricing post-exclusivity loss, and ensuring alignment across teams. The role also involves stakeholder management and communications with external pricing authorities.

Specialist position responsible for conducting patent searches, providing patent information, and acquiring patent rights to secure Freedom-to-Operate (FTO) for developing/commercial products at Santen. Requires more than 3 years of experience in patent practice/search, patent prosecution, search and dispute, and more than 5 years of experience in research/science. Must have language skills to communicate in English with internal and external stakeholders.

Lead the group accounting and financial reporting activities for Santen Group, focusing on IFRS principles and tax accounting. Manage team responsibilities, provide recommendations to superiors, utilize external resources efficiently, and contribute to financial operations and projects.

眼科医療に関する知識を活かし、マクロ環境調査、マーケティング戦略の立案から評価までを担当。市場分析に基づくKPI設定や営業ラインへの推進、関係構築も求められます。

The role involves developing and executing brand and medical plans, engaging with external medical experts, collecting insights for product evaluation, communicating drug information, participating in cross-departmental projects, and enhancing collaboration with other departments.

The Risk Management Manager in the Japanese Pharmacoe Epidemiology Team at Santen is responsible for overseeing risk management strategies and ensuring compliance with regulatory standards in the pharmaceutical industry. This role involves collaborating with various departments to implement effective risk mitigation measures and enhance patient safety.

The Analytical Sciences & Technology Manager supports analytical testing and product release for pharmaceutical products. Responsibilities include product manufacturing support, qualification and validation of analytical methods, improving testing methods, and managing compliance with international guidelines. The role involves collaboration with internal and external teams to ensure timely product release and adherence to quality standards.

The Senior Manager, Quality Management System will lead the development and implementation of the EMEA Quality Governance Structure and Quality Management System (QMS). Responsibilities include overseeing quality audits, deploying risk management processes, ensuring compliance with EU regulations, and supporting the operational tasks related to QMS in collaboration with leaders across the EMEA region.

生産技術職として医薬品製造ラインの新規開設、一貫した製品供給と品質向上に向けて技術移転や文書作成を行い、製造方法の設計と実行を担当します。