Executive Director, Regulatory CMC - Remote - USA

· We pioneer a moneyball for biotech approach pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. We build bridges to groundbreaking advancements in rare disease develop life-changing medi ...

We are seeking an Associate Director to join our team as a member of the Revolution Medicines team. This position is responsible for developing and implementing global CMC regulatory strategies. The role involves coordinating and preparing CMC sections of regulatory submissions t ...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. · ...

We are seeking an Associate Director of Regulatory Affairs CMC to develop and implement global regulatory strategies for assigned product(s) in line with business objectives. · ...

+Job summary · Senior Director, CMC Regulatory Affairs is responsible for leading the development, execution, and maintenance of global CMC regulatory strategy to support clinical development,+QualificationsAdvanced degree (MS, PhD, PharmD) in Chemistry...++Strategic Leadership- ...

The Senior Director, Regulatory CMC will provide strategic and operational leadership for CMC regulatory activities across both investigational and commercial products at Praxis Precision Medicines, · Advanced degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or ...

This position may be performed remotely, but requires the flexibility and willingness to travel as needed. · Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or a related scientific discipline (advanced degree preferred). · 5+ years of Re ...

+Job summary · The Senior Manager Regulatory CMC will be responsible for the planning preparation and execution of Chemistry Manufacturing and Controls CMC regulatory activities for investigational and commercial products including small molecule and antisense oligonucleotide ASO ...

Abdera Therapeutics is growing rapidly and seeking key new team members who thrive at the cutting-edge of innovation. · ...

This position will support outsourced manufacturing operations supporting Praxis's clinical and future commercial programs. · ...

The role of Director, Biologics will oversee process development and clinical production of radiolabeled monoclonal antibodies and conjugates within Telix's Global Operations organization. · ...

This position reports to the Functional Area Head, Global Regulatory Affairs. The incumbent is responsible for supporting the development and implementation of regulatory strategies. · Actively contribute to the development of regulatory strategies. · Participate as Global Produc ...

This is a mission-critical role for a bold and visionary leader committed to accelerating patient impact. · ...

This is a U.S. based remote role that will require quarterly, or as needed visits to our San Francisco Office. · ...

+ We're seeking a Principal Scientist in Process Chemistry to lead drug substance activities for one or more projects within Praxis' portfolio.+ · +Leads the Process Chemistry Research and Development for one or more projects from early to late phase within Praxis. · Designs both ...

+Job summary · The ideal candidate for this role is experienced in working closely with Contract Development and Manufacturing Organizations (CDMOs) that provide small molecule drug substance and drug product services to the pharmaceutical industry. · +QualificationsBachelor's de ...

Se busca un Sr. Manager para el desarrollo de productos farmacéuticos en BridgeBio. · ...

This position may be performed remotely but requires the flexibility and willingness to travel as needed. · ...

The Senior Quality Operations Manager, CMC is responsible for various operational activities to ensure product quality and compliance. They serve as the quality expert for Praxis pipeline of neurological disease product programs. · Oversee contract service providers (CSPs) for cl ...

The Senior Principal Scientist will serve as the technical authority and strategic leader for drug product development. · Own and lead the end-to-end drug product development strategy,Serve as the technical lead for all drug product activities with CDMOs,Provide strategic guidanc ...