대한민국.의 GSK 채용 정보

We are seeking a Senior Regulatory Affairs Specialist to join our team in Seoul. The successful candidate will be responsible for managing the registration and life cycle of existing products, including labelling updates and product license maintenance. · ...

The Senior Regulatory Affairs Specialist will be responsible for products registration and life cycle management of existing products. · ...

As Pharmacovigilance Specialist has overall responsibility for the day-to-day management of pharmacovigilance for marketed products and products in clinical trials. · ...

This position is responsible for providing Quality Assurance in enabling the GSK Quality requirements including all applicable local regulations. · The position holder is responsible in ensuring product launch and product supply to the market are safe, regulatory compliance and t ...

GSK is seeking an experienced and strategic Country Medical Director (CMD) to lead the Korea Medical organization and deliver medical solutions that improve patient outcomes. · ...

The Pharmacovigilance Specialist is responsible for the day-to-day management of pharmacovigilance for marketed products and products in clinical trials. · Bachelor's degree with a Medical science background. · Pharmacist (preferred). · More than 2 years of experience in Pharmaco ...

Products registration and life cycle management including timeline setup planning short- & long-term registration for NCE LE new indications establishment of strategy according to guideline amendments. · ...

This role supports the safe and effective use of GSK medicines by implementing aligned medical strategies generating actionable insights and facilitating cross-functional collaboration in the field of liver diseases. · ...

We are seeking an experienced Employee Relations & Industry Relations Manager/Professional to join our team in Korea. As a key member of our HR function, you will be responsible for developing and implementing employee relations policies and processes across the business. · Lead ...

The Senior Regulatory Affaist Specialist will lead registration planning for new products. · ...

This Regulatory Affairs Specialist role involves products registration management for existing products with timeline setup, · short & long-term registration planning for New Chemical Entities (NCE), Line Extensions, · Establishment of short- & long-term detailed registration pla ...

The Senior Regulatory Affaist Specialist will be responsible for managing regulatory issues related to existing products including registration planning and maintenance of product licenses. · ...

GSK is seeking an experienced and Senior Director External Partnerships Oncology (ASIA) that is reporting to the Head of Academic and Scientific Partnerships Oncology. · ...

This position provides Quality Assurance enabling GSK Quality requirements including all applicable local regulations but not limited embedded complied its own working operations executing areas product launch product supply market safe regulatory compliance timely manner. ...

This QA Specialist position at GSK involves providing quality assurance in enabling the company's quality requirements while ensuring product launch and supply are safe and timely. · Pharmacist, mandated by local regulation to certify product releaseAt least 3 years of working ex ...

You will support the brand team in Korea to plan and deliver customer-focused marketing activities. · ...

This position is responsible for providing Quality Assurance in enabling the GSK Quality requirements including all applicable local regulations. The position holder is responsible in ensuring product launch and product supply to the market are safe, regulatory compliance and tim ...

GSK is seeking a Senior Director to lead external partnerships in oncology across Asia. · Establish global team and operationalise new Global team with Asia-specific ways of working · Strategic planning and partnership leadership for high-impact partners in China and Japan · ...

To engage and build strong, credible, and long-term scientific partnerships with key external medical experts across GSK's Hepatology portfolio by delivering high-quality, · Serve as the primary field-based scientific expert representing GSK Medical and Hepatology medical strateg ...

This position is responsible for providing Quality Assurance in enabling the GSK Quality requirements including all applicable local regulations. · Review the batch release of Rx products. · Approve the pharma products release as Qualifed Person (QP). · ...