Regulatory Affairs Jobs in Thailand

Role Purpose The AMEA 3rd Party Supply Chain Operations Lead manages end-to-end P&S implementation of 3rd party projects across Asia-Pacific Middle East and Africa covering both purchase-for-resale (PfR) and active ingredient (AI) in-licensing deals with external partners. The role drives cross-func...

JOB DESCRIPTION:Main Purpose of the RoleThe Country Manager Thailand Cambodia Laos and Myanmar will take P&L responsibility for building an effective sales pipeline which will result in achieving strategic & financial goals in his or her region.This position is key in managing the sales marketing...

What you will doKOL Engagement and Relationship ManagementIdentify establish and maintain productive relationships with KOLs healthcare professionals and academic institutions within the assigned therapeutic area.Collaborate with KOLs to gather insights feedback and medical/ scientific information t...

ROLE SUMMARYLead medical to medical communications in the field. This role considered as field base medical activities.The Medical Science Liaison is responsible for the development ofKOLstakeholderstrategy execution ofexternal medicalengagementwith designated portfolio within ThailandThe Medical Sc...

Job SummaryAre you passionate in developing and growing sales portfolio for industry leading customers Do you aspire to be part of the team that drives big wins for a global organizationIFF is a global leader in flavors fragrances food ingredients and health & biosciences we deliver sustainable inno...

JOB DESCRIPTION:MAIN PURPOSE OF ROLEThe APAC senior regulatory manager supports the APAC RA Director in the daily activities related to product registration tracking and lifecycle maintenance.This position ensures that product registrations across APAC countries are progressing according to timeli...

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JOB DESCRIPTION:Primary Job Function: The APAC senior regulatory manager supports the APAC RA Director in the daily activities related to product registration tracking and lifecycle maintenance.This position ensures that product registrations across APAC countries are progressing according to time...

Job Overview: Under general supervision prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients. Provides regulatory support for assigned projects.Essential Functions:Acts as a Regulatory Te...

Job SummaryRegulatory Affairs Specialist will oversee the preparation and submission of regulatory dossiers ensuring compliance and timely approvals. This role is pivotal in managing activities pertaining to product lifecycle management quality management and pharmacovigilance including variations a...