We need your talent, knowledge and dedication to better our world with biology. · Support fresh dairy application test (e.g. making yogurt from fresh milk) · Support test result analysis (e.g. cell count, sensory test) · Assist basic lab chores (e.g cleaning lab and equipment, mi ...

Project Engineer responsible for determining project scope, developing preliminary plans, and communicating with clients to promote and explain services. · ...

Deliver product demonstrations of GCM to customers, respond to inquiries, and effectively communicate the value of the service. Gather and understand customer needs, and proactively provide feedback to the GCM project team to contribute to service quality improvements and ongoing ...

Join our dynamic lab at the RIKEN Center for Brain Science, where we unravel the regulatory mechanisms of neuron specification and differentiation - key processes that build the nervous system and, when disrupted, lead to neurodevelopmental disorders and age-related degeneration. ...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and profess ...

Deliver product demonstrations of GCM to customers, respond to inquiries, and effectively communicate the value of the service. · Provide product demonstrations to customers, respond to inquiries, and communicate the value of the service. · Understand the basic logic behind prici ...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and profess ...

This is a key middle management role with both local and global impact at Ferring Pharmaceuticals, offering a unique opportunity to contribute to both local GQP/QA operations and global Quality Management System (QMS) initiatives and the operations. · Influence both local and glo ...

The Clinical Research Associate II will be responsible for site management, conducting site monitoring responsibilities, and preparing project plans related to clinical monitoring. The ideal candidate will have a thorough understanding of ICH GCP Guidelines and local regulatory r ...

Toyota is seeking a Regulation & Certification Assistant Manager to support internal developers in terms of legal and regulatory compliance and acquiring certificates from governments. The successful candidate will define policies and processes to investigate regulatory requireme ...

We are seeking a Regulation & Certification Assistant Manager to support our compliance and internal assessment of novel services for use in the city. The successful candidate will define policies and processes to investigate regulatory requirements, guide engineering teams to sa ...

Join our dynamic team as a CMC (chemistry, manufacturing, and controls) Expert, where you will play a pivotal role in shaping regulatory strategies and ensuring high-quality submissions to authorities like PMDA/MHLW. Leverage your expertise to collaborate with global teams, shari ...

Toxicology expert responsible for assessing preclinical toxicology data, ensuring safety of volunteers and patients in clinical trials, and preparing toxicology documentation. · ...

We are hiring for a CAR-T Cell Collection Technician/Supervisor to be located in Japan and reporting to the manager in APAC region. This individual will support the establishment and implementation for apheresis and cryopreservation operations. · This role fully accountable to es ...

We are hiring for a CAR-T Cell Collection Supervisor, CAR-T Regional Supply Chain, Manufacturing and Supply Div. The role is responsible for managing contracts and communication with third-party suppliers in APAC countries. This individual will support the establishment and imple ...

Join our dynamic team as a CMC Expert, where you will play a pivotal role in shaping regulatory strategies and ensuring high-quality submissions to authorities like PMDA/MHLW. · Prepare high-quality J-QOS documents, application sheets, and responses to inquiries from PMDA/MHLW in ...

Lead, Local Trial Manager is a senior trial management role with at least 4 years of clinical trial management experience or more than 6 years of clinical monitoring experience. This role is responsible for local management of a clinical trial (or Medical Affairs data generation ...

A Senior, Local Trial Manager is a mid-level trial management role with typically at least 2 years of clinical trial management or 3-5 years for clinical monitoring experience. This role is responsible for local management of a clinical trial (or Medical Affairs data generation a ...

We are currently recruiting for an External Manufacturer Quality Lead. · ...

+A Project Engineer at Underwriters Laboratories is responsible for determining project scope, developing preliminary plans, and coordinating laboratory activities. · +Determines project scope and develops preliminary plans. · Coordinates laboratory activities by preparing data s ...

Join our dynamic lab at the RIKEN Center for Brain Science, where we unravel the regulatory mechanisms of neuron specification and differentiation - key processes that build the nervous system and, when disrupted, lead to neurodevelopmental disorders and age-related degeneration. ...