Executive Director, Regulatory CMC - Boston

Director, Regulatory Affairs - CMC (Individual Contributor) · Location: Flexible (U.S. based only, remote or hybrid options available) · Employment Type: Full-time · Summary: · A growing biopharmaceutical company is seeking a Director, Regulatory Affairs - CMC to lead global regu ...

SciPro partnered with a late-stage biotech seeking a Director, Regulatory CMC to join their team full-time. · This role leads global regulatory strategies and guides submissions ensuring compliance throughout product lifecycle. · ...

SciPro is partnered with an exciting late-stage biotech that is seeking a Director, Regulatory CMC to join their team full-time. · ...

Director, Regulatory Affairs - CMC (Individual Contributor) · Location: Flexible (U.S. based only, remote or hybrid options available) · Employment Type: Full-time · Summary: · A growing biopharmaceutical company is seeking a Director, Regulatory Affairs - CMC to lead global regu ...

Antares Therapeutics is seeking an experienced Regulatory Affairs–CMC Strategist (Consultant) to provide senior strategic advisory leadership for global, phase-appropriate CMC regulatory strategies supporting early-stage small molecule product development. · Advanced degree (PhD, ...

At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailer ...

We are growing our Regulatory Affairs organization and are seeking a proactive and detail‑oriented professional to support global Regulatory CMC activities across our clinical programs.This is an exciting opportunity to contribute to high‑impact development efforts within a fast‑ ...

We are seeking a Director of Regulatory Affairs, CMC to support the development and execution of global regulatory strategies in the field of pharmaceuticals. The ideal candidate will have experience providing strategic regulatory guidance to drug development teams. · ...

We are looking for an Associate Director, Regulatory CMC to work closely with cross-functional subject matter experts to provide strategic and operational input for CMC regulatory activities including submissions, reviews, and health authority interactions. · ...

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 ...

At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. · We are passionate about creating an inclusive workplace that promotes collaboration, integrity, and exce ...

+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 ...

At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailer ...

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· Centessa Pharmaceuticals plc (Nasdaq: CNTA) new kind of pharmaceutical company with a deconstructed R&D environment that prioritizes data driven decision making led by subject matter experts. Centessa is advancing a portfolio of high conviction programs with strong biological ...

The Director Regulatory Site CMC ensures efficient and compliant management of regulatory change control and post-approval activities at the site level. This includes leading site-specific post-approval change management activities, applying science- and risk-based approaches to ...

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 ...

Amylyx has an audacious mission to usher in a new era for treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitment to the communities we serve. · ...

We are seeking an experienced and forward-thinking Director, Regulatory Affairs to lead global regulatory strategy and execution across both CMC and clinical development programs. · Provide strategic Regulatory CMC leadership across Generate's biologics portfolio, · Lead the plan ...

Amylyx Pharmaceuticals busca un Associate Director, Regulatory CMC para desarrollar estrategias y operaciones regulatorias en proyectos identificados. El rol trabaja estrechamente con equipos internos y externos para avanzar la cartera del compañía. · Sueldo competitivo según exp ...