Santen
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Manage integrated, cross-functional project timelines and budgets in collaboration with the Project Manager to drive efficient delivery. Collaborate cross-functionally to collect key insights related to project status, assess actual performance against planned, and prepare reports to inform on potential risks to delivery. Proactively identify, escalate, and manage project risks and issues. Manage meeting logistics, including scheduling, documentation of minutes, ADI logs, etc. Ensure all projects comply with Santen project management policies and standards.
Manage global GxP audit function and develop the organization to implement standardized GxP audit procedures. Build consensus and collaborate with cross-regional quality functions. Establish quality systems, SOPs, and procedures for GxP audit compliance.
Responsible for timely registration of new products, regulatory submissions, development of registration strategies, and monitoring changes in local regulations. Requires over 5 years of experience in local regulatory affairs with in-depth knowledge of legislation and registration procedures.
Managing statistical analysis for clinical trials and research studies, contributing to study planning and communication, and collaborating with stakeholders in the pharmaceutical industry.
Develop and implement sales strategies, analyze market trends, set sales targets, lead sales team, build relationships with key customers, identify new business opportunities, collaborate with marketing team, manage sales budget effectively.
The Process Engineer position at Santen involves providing engineering support to manufacturing production, driving process improvement activities, and implementing lean manufacturing principles to enhance operations.