Director, Regulatory Site CMC - Boston, MA

+Takeda,+we+are+a+forward-looking,+world-class+R&D+organization+that+unlock+sustainability+,delivering transformative therapies to patients worldwide. · The Director Regulatory Site CMC ensures efficient management of regulatory change control activities at site level. · This pos ...

We are looking for someone with strong practical experience with global HA requirements, beyond EU/US. · The Director Regulatory Site CMC ensures efficient and compliant management of regulatory change control and post-approval activities at the site level.This position leverages ...

+The Director Regulatory Site CMC ensures efficient and compliant management of regulatory change control and post-approval activities at the site level. · Lead site-specific post-approval change management activities... · ...

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use.  I further attest that all information I sub ...

We are seeking an experienced CMC Regulatory Lead to provide strategic and operational leadership for all Chemistry, Manufacturing, and Controls (CMC) regulatory activities. · Develop and execute global CMC regulatory strategies to support IND, CTA, NDA/BLA, and lifecycle submiss ...

We are seeking a highly experienced Vice President, Regulatory Affairs, CMC to provide strategic and operational leadership for global CMC regulatory activities across a growing pipeline of innovative therapeutics. · We seek a recognized subject matter expert in Regulatory Affair ...

We are seeking a highly experienced Senior Vice President, CMC Regulatory Affairs to provide strategic and operational leadership for global CMC regulatory activities across a growing pipeline of innovative therapeutics. · This role is designed for a recognized subject matter exp ...

+We are seeking a highly experienced Vice President, Regulatory Affairs, CMC to provide strategic and operational leadership for global CMC regulatory activities across a growing pipeline of innovative therapeutics. · +Define and lead the global CMC regulatory strategy across all ...

We are seeking an experienced and strategic Executive Director to lead global regulatory strategy for pharmaceutical and biotechnology development programs. This role requires cross-functional collaboration with various teams including Technical Operations, Quality, Clinical, and ...

We are seeking an experienced and strategic Senior Director, Regulatory Affairs – CMC to lead global CMC regulatory strategy across a diverse portfolio of small molecule and biologic development programs from early clinical development through commercialization. · This role is a ...

Lensa does not hire directly for these jobs but promotes jobs on LinkedIn behalf of its direct clients recruitment ad agencies marketing partners. · ...

We are seeking an experienced and strategic Senior Director Regulatory Affairs – CMC to lead global CMC regulatory strategy across a diverse portfolio of small molecule and biologic development programs from early clinical development through commercialization. · ...

We are seeking an experienced Associate Director, Regulatory Affairs CMC to serve as the Regulatory CMC Lead for a late-stage small molecule development program. · This individual will be responsible for providing strategic regulatory direction and managing CMC related activities ...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. This role is within in the GRA Chemistry Manufacturing & Controls (CMC) organization. · We at Takeda are transforming patient care through novel specialty pharmaceutical ...

We're not just looking for the brightest minds or for the most brilliant individual contributors.We want passionate team members who are comfortable adjusting their lens, aren't afraid to think big, test bold ideas, and celebrate collective wins. · ...

This CMC and QA leadership role is key to progressing HotSpot's programs to clinical development. · This CMC and QA leadership role is key to progressing HotSpot's programs to clinical development. · ...

We are seeking a Director, Regulatory Affairs to join our team. This position reports to the Executive Director and will be based out of Boston in our Needham office. Responsibilities include proposing and implementing global CMC regulatory strategies and providing guidance to cr ...

This CMC and QA leadership role is key to progressing HotSpot's programs to clinical development. · In consultation with senior advisors, lead CMC strategy and execution to support delivery of HotSpot development programs. · ...

We are seeking a Sr. CMC Project Manager to join the Technical Operations Program & Strategy team at Apogee. This role is responsible for handling all CMC related documentation. · Lead the documentation flow between Tech Ops and our partners. · Maintain and communicate a current ...

The Chief of Staff will drive the execution of Pharm Sci strategy to increase business performance. They will partner with PS, partners and leadership to identify and lead enterprise-wide transformation initiatives. · Drive the execution of Pharm Sci strategy. · Partner with PS, ...