Regulatory Affairs Jobs in Taiwan

Work Flexibility: HybridHelp bring innovative medical technologies to patients by driving regulatory excellence across the product this role you will shape registration strategies navigate evolving regulatory landscapes and ensure compliant timely access to lifechanging devices. If you thrive in a...

Job DescriptionWHAT YOU WILL DO- Support Medical Affairs team in the execution of medical programs and initiatives.- Assist in the review and analysis of medical literature research findings and clinical data.- Help ensure compliance with regulatory standards and guidelines in all medical activities...

The Business Unit Director (BUD) will be the strategic and operational leader for AbbVie Taiwans assigned business unit. This role holds full P&L accountability responsible for shaping and executing a long-term growth strategy while ensuring short-term commercial excellence.As a key member of the Ta...

If youre interested in this role please apply in English and include an English version of your Resume/CV.The RoleJoining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. M...

About the roleThe Trade Compliance Analyst is responsible for data analysis operations management and/or system configuration of Trade Compliance activities. This can be at site or global level. Report directly to the Head of Global Trade Compliance.What you will doCollaborate with cross-functional...

Established in 1987 Air Liquide Far Eastern (ALFE) is a prominent joint-venture between Air Liquide Group a global leader in gases technologies and services for Industry and Health and Far Eastern New Century recent years ALFE has emerged as the top French company in terms of investment in Taiwans...

JOB SUMMARYRegulatory Affairs Specialist is responsible for the implementation of clinical trial application and product life-cycle management in compliance with local regulations and Company Standard Operating Procedures (SOPs).JOB RESPONSIBILITIESProduct life-cycle management & GMP maintenance- En...

Business IntroductionAt GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

JOB DESCRIPTION:Main Responsibilities:Responsible for managing new and variation registrations securing approvals at the earliest possible time and effectively allocating resources to support the achievement of Abbott Diagnostics Taiwans objectives. Oversee lifecycle activities such as renewals no...

JOB SUMMARYHub Labeling Associate is responsible for supporting Labeling Managers by maintaining documentation in labeling systems so that SOP requirements are fulfilled. Maintains workflow management tools and mailboxes and associated technical support.JOB RESPONSIBILITIES Supports Hub Labeling Man...

JOB SUMMARYSenior Regulatory Sciences Specialist is responsible for end-to-end regulatory strategic activities of product registration life-cycle management in compliance with local regulations and Company Standard Operating Procedures (SOPs).What You Will AchieveIn this role you will:- Provide stra...

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Primary Function of PositionThis role is responsible for supporting developing and implementing clinical strategies designing and executing clinical studies in the APAC across surgical specialties and various product platforms. This role will oversee and manages clinical protocols and other key stud...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.A Day in the LifeResponsibilities may include the following an...

JOB DESCRIPTION:KEY RESPONSIBILITIESRegulatory AffairsPrepare submit and obtain approvals for medical device licenses and other relevant permits from the Taiwan authorities for assigned products.Coordinate and maintain correspondence with Corporate Regulatory Affairs and Subject Matter Experts.Man...