日本のPlanet Pharmaの求人

The Medical Advisor serves as an internal scientific authority for a designated product or therapeutic area. · Develop and implement the annual Medical Plan · ...

A global clinical research organisation is seeking experienced Clinical Research Associates to support clinical trial delivery across Japan. · ...

A leading global pharmaceutical manufacturer is seeking an experienced Automation Architect (Lead) to support a major greenfield OSD manufacturing facility project in Japan. · ...

Medical Science Liaisons (MSLs) are field-based members of the Medical Education function and act as scientific ambassadors for the organization. · ...

A global clinical research organisation is seeking an experienced Associate Director / Director of Clinical Monitoring to lead and scale its Clinical Monitoring function in Japan. · ...

A regulated pharmaceutical organisation is seeking a Pharmacovigilance (PV) Associate to support its drug safety and pharmacovigilance operations in Japan. · ...

A life sciences organisation is seeking a Regulatory Affairs Associate to provide hands-on administrative and documentation support to the Regulatory Affairs function in Japan. This role plays a key supporting role in regulatory project coordination, documentation quality, and su ...

A global pharmaceutical manufacturing organisation is seeking a senior Automation Engineer to support the delivery of a large-scale greenfield OSD facility in Japan. · ...

An established pharmaceutical manufacturing organisation is seeking an experienced Electrical Engineer to support operations within a sterile manufacturing environment. · Design, implement, and maintain electrical systems within the manufacturing facility · Provide technical expe ...

A global clinical research organisation seeks an experienced Regulatory Submissions Manager to support clinical trial start-up and regulatory submission activities in Japan. · Lead and execute regulatory start-up activities for global and local clinical studies · Perform quality ...

The Clinical Trial Manager is responsible for supporting and/or leading the planning, set-up, · and execution of assigned clinical trials.The role works closely with cross-functional internal teams and external vendors to ensure trials are executed efficiently, · compliantly,and ...

The Project Scheduler is responsible for preparing and maintaining both high-level and detailed CPM schedules across design, procurement, construction, commissioning, · and integrated Design-Build / EPCM projects.Bachelor's degree in Construction, Engineering, · or a related fiel ...

The Planet Group of Companies is seeking a Senior Process Lead to support greenfield pharmaceutical manufacturing facility projects in Japan. The ideal candidate will have extensive experience in Oral Solid Dosage (OSD) production environments and a strong background in GMP compl ...