Regulatory Submission Management Lead

Job Title: Associate Director, Regulatory Submission ManagementAbout the Role:We are seeking an experienced Associate Director to lead our Regulatory Submission Management team. As a key member of our Global Regulatory Affairs team, you will be responsible for planning, managing, and tracking regulatory submissions across multiple programs.Key...

Job Title: Principal Regulatory Affairs SpecialistWe are seeking an experienced Principal Regulatory Affairs Specialist to play a key role in supporting regulatory strategies and ensuring the success of our diagnostic products in the global market.Key Responsibilities:Regulatory Submissions and Documentation: Prepare and manage regulatory submissions,...

We are seeking an Associate Director, Global Regulatory Affairs to lead our global regulatory strategy in Cambridge, MA.Takeda Development Center Americas, Inc. is a leading pharmaceutical company that prides itself on innovation and excellence in the field of immunology and inflammation therapeutic franchise.The ideal candidate will have a Master's degree...

Unlock Your Potential in Global Regulatory AffairsTakeda is a patient-focused company that transforms patient care through novel specialty pharmaceuticals and best-in-class patient support programs.As an Associate Director, Global Regulatory Project Management and Strategic Planning - GI2 TAU, you will be part of our Global Regulatory Affairs organization,...

About the RoleWe are seeking a highly skilled Global Regulatory Lead to join our team at Takeda Pharmaceutical. As a key member of our organization, you will play a critical role in defining and executing global regulatory strategies to drive business success.Job DescriptionThis is a hybrid position that requires collaboration with cross-functional teams to...

As a key member of the Global Regulatory Team at Takeda Pharmaceutical, you will play a critical role in defining and leading global strategies for regulatory success. With your expertise in pharmaceutical industry experience and regulatory affairs, you will ensure compliance with applicable requirements, lead cross-functional initiatives, and contribute to...

Regulatory Affairs ConsultantCapgemini is seeking a highly skilled Regulatory Affairs Consultant to manage and optimize our regulatory information management processes using the Veeva Vault RIM platform. The ideal candidate will have a strong background in regulatory affairs, experience with Veeva solutions, and a deep understanding of compliance...

About the PositionWe are seeking a seasoned Global Regulatory Project Manager to join our team in Massachusetts, USA. As a key member of our Global Regulatory Affairs organization, you will be responsible for managing global regulatory projects from late stage filings.Key ResponsibilitiesPartner with the Global Regulatory Lead to ensure seamless execution of...

Transformative Therapies for a Brighter FutureWe are Takeda, a forward-thinking global R&D organization dedicated to unlocking innovation and delivering life-changing therapies to patients worldwide.About the Role:We invite you to join our team as a Senior Director, GRA CMC Pharmaceuticals Development Portfolio Lead. In this pivotal position, you will...

At Best Buy Health, we're committed to enriching and saving lives through technology and meaningful connections.We're seeking a seasoned Regulatory Affairs Manager to join our team in Boston, MA. This is a full-time position that offers a competitive salary of $120,000 per year.Job Description:Develop and implement comprehensive global regulatory strategies...

About the Role: We are seeking a seasoned Technical Regulatory Advisor to lead our pharmaceutical innovations team. As a key member of our global regulatory affairs department, you will be responsible for defining and implementing an external engagement strategy, governance, and associated capabilities in line with Takeda's patient-centric values.Key...

About the RoleWe are seeking an experienced Senior Director, Regulatory Affairs to join our team at AVEO Oncology. In this role, you will be responsible for developing and executing global regulatory strategies in support of our development programs.Job SummaryThe successful candidate will provide strategic insights and planning as well as guidance and...

Job OverviewRQMIS Inc, a leading medical device/biotechnology consultancy, is seeking an experienced Regulatory Documentation Specialist to join our team in Amesbury, MA. As a key member of our team, you will play a crucial role in supporting projects involving labeling, regulatory submissions, quality system documentation, and clinical study material.Key...

About the RoleWe are seeking an experienced Global Medical Devices Regulatory Compliance Expert to join our team at Best Buy Health. In this role, you will be responsible for ensuring the global regulatory compliance of medical devices throughout their lifecycle, from development to post-market surveillance.Key Responsibilities:Develop and implement...

About the CompanyTakeda Pharmaceutical is a patient-focused company dedicated to delivering innovative treatments and improving healthcare worldwide.Job SummaryWe are seeking an experienced Global Labeling Lead to join our team in Massachusetts. As a key member of our regulatory affairs department, you will be responsible for developing and implementing...

About the OpportunityWe are seeking a seasoned Regulatory Affairs Professional to join our Global Regulatory Affairs CMC team as a Director, GRA CMC Small Molecules. This role offers an exceptional opportunity to contribute to the development and execution of regulatory strategies for our small molecule products.Job Summary:Oversee the development and...

Job SummaryWe are seeking an experienced Global Regulatory Affairs Strategist to join our team at Takeda Pharmaceutical. In this role, you will be responsible for defining, developing, and leading global strategies to maximize regulatory success towards achievement of program objectives for complex and/or multiple projects.ResponsibilitiesProvide strategic...

Welcome to Takeda Pharmaceutical, where we are committed to creating a diverse and inclusive workplace culture that fosters innovation and growth.As a Director of Regulatory Compliance, you will be responsible for developing and implementing regulatory strategies to ensure compliance with global regulations and guidelines. Your expertise in CMC regulations...

Transform Patient Care with Takeda Pharmaceutical. We're seeking a highly skilled Associate Director, Global Regulatory Affairs Marketed Products to lead complex projects and ensure global regulatory compliance.**Job Summary:**This role is responsible for defining, developing, and leading global strategies to maximize regulatory success for complex projects....

Job OverviewTakeda Pharmaceutical is seeking a skilled Global Regulatory Affairs Compliance Lead to join our team in Zurich, Switzerland or Massachusetts. This is a full-time opportunity.About the RoleWe are looking for a highly motivated and experienced professional to lead our global regulatory affairs compliance efforts. The successful candidate will be...