Tokyo Gilead Sciences

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description
Company Overview
At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Position Overview

  • May serve as a Core member of the cross-functional PDM Project Team (region specific).
  • Regional Regulatory Lead on Regulatory Project Teams.
  • Regional Lead and may lead cross-functional /cross- regional Regulatory Submission Teams.
  • Participates on other Subteams, as applicable.
  • Serves as contact with local Regulatory Authorities.
  • Some positions at this grade level may partially or wholly include oversight of computerized systems.

Job Responsibilities

  • Responsible for preparing and/or overseeing the preparation of technically complex regulatory CMC submissions which require extensive interaction with departments outside of Regulatory Affairs CMC for investigational and commercial products, in line with ICH requirements, regional requirements and scientific and company policies and procedures. Examples include supplements and license renewals to clinical trial applications and marketing authorizations, and CTNs for assigned territories.
  • Provides strategic regulatory CMC advice as appropriate.
  • Oversees preparation and maintenance of country specific labeling and product packaging (region specific).
  • Coordinate and facilitate development of regional Regulatory CMC strategy with affiliates for local meetings and interactions.
  • Ensures up-to-date knowledge of regulatory CMC. requirements and communicates relevant changes in regulatory information to project teams and senior management in a timely manner.
  • Initiates local process improvements and contributes to local and / or global process improvements, which have a significant impact for the Regulatory Affairs CMC Department or other departments.
  • Plans, schedules and arranges own activities and those of direct reports (if applicable).

Knowledge & Skills

  • Excellent organizational skills and ability to work on and/or oversee a number of projects with tight timelines.
  • Excellent verbal and written communication skills and interpersonal skills.
  • In-depth knowledge of regulatory requirements, including ICH requirements and regional requirements for assigned territories and have an in-depth understanding of current global and regional trends in Regulatory Affairs CMC.
  • Capable of developing and implementing regulatory strategy and of managing complex negotiations with Regulatory Authorities.
  • Capable of assuming leadership role in updating and preparing the Company for minor changes in legislation in assigned territories and of actively participating in a broader cross functional team for implementation of major changes (region specific).
  • Capable of leading a team in preparation of complex regulatory submissions and maintenance of licenses.
  • Work is performed under consultative direction towards corporate regulatory goals and objectives.
  • Is recognized as a knowledgeable resource for CMC Regulatory Advice in other departments.

Education & Experience

  • 10+ years of experience in Regulatory Affairs CMC or other relevant industry experience with advanced degree.
  • Degree in a scientific field is preferred.

For Current Gilead Employees And Contractors
Please apply via the Internal Career Opportunities portal in Workday.



  • Japan - Tokyo Gilead Sciences ¥5,000,000 - ¥10,000,000 per year

    This is an opportunity to join Gilead's Regulatory Affairs team as Associate Director for Regulatory Affairs CMC. As a key member of our team you will be responsible for preparing and overseeing regulatory submissions and providing strategic advice on regulatory matters. · Respon ...


  • Tokyo Gilead Sciences ¥5,000,000 - ¥15,000,000 per year

    At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the glob ...


  • Japan - Tokyo Amgen

    head of Japan regulatory strategy for oncology and rare disease responsible for developing executing regulatory strategies effective key regulatory agency interactions ensuring local labels are developed maintained line with local legislation amgen standards procedures supervisor ...


  • Shinjuku Cordis Full time¥5,000,000 - ¥10,000,000 per year

    This position will be responsible for leading all medical device Regulatory Affairs activities which include product submissions, develop regulatory strategies, change assessments, commercial supports, compliance related activities, systems/process improvements and other responsi ...


  • Tokyo APCO ¥10,000,000 - ¥30,000,000 per year

    APCO Worldwide—a global advisory and advocacy firm - is looking for a dynamic public affairs professional to drive APCO's Japan business with a broad range of international Technology/healthcare clients. · ...


  • Tokyo, Japan APCO Worldwide Holdings

    APCO Worldwide—a global advisory and advocacy firm—is looking for a dynamic public affairs professional to drive APCO's Japan business with international Technology/healthcare clients. · Drive APCO's Japan business with international Technology/healthcare clients. · Manage large ...


  • Tokyo Talisman Corporation

    The company is a leading firm for rare diseases. · Quality professional with strong subject knowledge, both in depth and breadth. · ...


  • Tokyo IFF ¥60,000 - ¥120,000 per year

    Are you passionate about advancing health and wellness through innovative bioscience solutions? · Channeling our passion for nature and bioscience into sustainable, life-enhancing technologies that power innovative solutions across healthcare, food, consumer and industrial market ...


  • Tokyo Regeneron Pharmaceuticals ¥5,000,000 - ¥10,000,000 per year

    We are Regeneron: A leader in medical innovation driven by a commitment to improving lives. Join our Medical Affairs team as an Associate Director in Field Medical Affairs and make a meaningful impact in oncology. · ...


  • Tokyo Talisman Corporation ¥5,000,000 - ¥15,000,000 per year

    The Director of Global Regulatory Chemistry, Manufacturing, · & Controls (GRA-CMC) will be responsible for developing and implementing global · CNC regulatory strategy leading to successful registration and life-cycle management. · May lead individual teams (people manager).Lead ...


  • Tokyo Organon Full time¥150,000 - ¥250,000 per year

    We are seeking an Associate Director to join our Japan Regulatory Affairs team. The successful candidate will be responsible for developing new drug regulatory strategy for Japan and collaborating with commercial and local stakeholders to align regional regulatory strategy with c ...


  • Tokyo APCO ¥1,200,000 - ¥1,600,000 per year

    APCO Worldwide—a global advisory and advocacy firm—is looking for a dynamic public affairs professional to drive APCO's Japan business with international Technology/healthcare clients. · ...


  • Japan - Tokyo Gilead Sciences ¥4,000,000 - ¥6,000,000 per year

    We're creating a healthier world for all people at Gilead. We tackle diseases like HIV and cancer – developing therapies that help improve lives. · This position reports to the Therapeutic Area Lead. · Collaborate closely with other teams to execute medical activities. · ...


  • Tokyo Gilead Sciences ¥6,000,000 - ¥12,000,000 per year

    We believe every employee deserves a great leader. · This position reports to the Therapeutic Area (TA) Lead for HIV & COVID-19 · ...


  • Hino GE HealthCare ¥6,000,000 - ¥12,000,000 per year

    Provides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations and postmarket compliance. · ...


  • Hino GE HealthCare Full time¥6,000,000 - ¥12,000,000 per year

    Provides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations and postmarket compliance, working closely with healthcare regulatory bodies globally. Impacts quality of own w ...


  • Hino, Tokyo GE HealthCare ¥4,000,000 - ¥8,000,000 per year

    Provides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations and postmarket compliance, working closely with healthcare regulatory bodies globally. Impacts quality of own w ...


  • Yokohama GE HealthCare ¥6,000,000 - ¥12,000,000 per year

    Provides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations and postmarket compliance, working closely with healthcare regulatory bodies globally. · Provides regulatory in ...

  • RA Manager

    4日前


    Tokyo Barrington James

    · 新薬・後発品(ジェネリック)の導入・維持管理を薬事の立場から担当 · 日本を含むグローバルのプロジェクトチームと連携し、薬事戦略の立案・進行管理を行う · ...


  • Tokyo, Tokyo Planet Pharma ¥4,000,000 - ¥8,000,000 per year

    The Senior Regulatory Affairs – CMC Specialist will be responsible for leading and supporting Chemistry, Manufacturing, and Controls (CMC) regulatory activities related to product development, registration, and lifecycle management for the Japanese market. · Author, review, and m ...


  • Tokyo, Tokyo Ipsen ¥5,000,000 - ¥10,000,000 per year

    The CMC Regulatory Strategy Manager will coordinate the CMC regulatory strategy activities for assigned projects, manage the CMC Regulatory relationship with Global CMC, and execute CMC Module finalization of J-NDA. The role will also lead the development of CMC regulatory strate ...