Director, Regulatory Affairs Jobs

Transform regulatory affairs by leading global strategy for oncology programs. Partner cross-functionally to navigate IND submissions and health authority interactions, ensuring successful Phase 1 and...

Lead strategic regulatory CMC initiatives, managing submissions and risk assessments for clinical and commercial products. Collaborate cross-functionally to drive compliance and optimize dossier conte...

Contribute to regulatory CMC strategies for drug development and commercialization. Lead global submissions, ensure compliance with health authority standards, and engage cross-functional teams for ri...

Drive regulatory strategies for product compliance in the LACAR Region. Lead global regulatory operations, product registration efforts, and collaboration with cross-functional teams to ensure adheren...

Unlock potential by managing complex regulatory projects, ensuring quality deliverables, and leading cross-functional initiatives. Utilize your expertise to provide strategic consultancy and complianc...

Lead and manage complex regulatory projects, ensuring quality delivery on time and within budget while providing strategic consultancy and maintaining compliance across multiple functions and diverse...

Lead the charge in managing large, complex regulatory projects, ensuring quality deliverables while overseeing cross-functional teams, driving strategic consultancy, and innovating solutions for compl...

Drive regulatory CMC strategies and submissions for generic drugs, ensuring compliance with FDA regulations. Collaborate with cross-functional teams to facilitate timely approvals throughout the produ...

Elevate your career with a leadership role in Regulatory Affairs CMC, driving global strategies for gene therapy products. Collaborate cross-functionally, ensuring regulatory compliance while supporti...

Champion the development of regulatory strategies for CMC in gene therapy, facilitating cross-functional collaboration and ensuring compliance while guiding innovative products through clinical to com...

Lead regulatory strategy for innovative CAR T and gene therapy programs, ensuring compliant submissions and fostering collaboration across cross-functional teams to navigate complex clinical landscape...

Unlock your potential in CMC regulatory leadership, driving strategies and managing global submissions for late-stage clinical assets while collaborating across functions to ensure compliance and time...

Shape global CMC regulatory strategies, lead submissions, engage with stakeholders, and drive compliance for cell therapy products in a fast-paced, collaborative environment, ensuring successful devel...

Take ownership of CMC regulatory strategies, ensuring compliance and driving product development by collaborating across teams and engaging with regulatory authorities to support key initiatives and s...

Collaborate with cross-functional teams to develop regulatory strategies for CMC. Ensure compliance and drive success for pipeline products by overseeing the preparation and submission of critical reg...

Champion regulatory strategy and execution for early-stage development programs, serving as the Global Regulatory Lead and primary contact with health authorities to ensure compliance and effective en...

Join a team that's shaping global regulatory strategies for innovative medical devices, ensuring compliance and excellence in quality assurance while leading cross-functional collaborations to deliver...

Join a team that drives regulatory excellence for clinical development, ensuring strategic and compliant submissions. Collaborate cross-functionally to accelerate drug approval processes while oversee...

Transform regulatory operations by leading submission strategies, managing systems, and ensuring compliance across portfolios while collaborating with cross-functional teams for successful outcomes...

Lead and drive global regulatory publishing operations, ensuring compliance and quality for submissions across multiple regions. Collaborate with cross-functional teams to enhance processes and suppor...

Take ownership of regulatory advertising and promotion strategies, ensuring compliance with FDA requirements and alignment with corporate goals. Lead cross-functional collaborations in a fast-paced, d...

Join a dynamic team and take ownership of regulatory activities for various pharmaceutical products, providing guidance and ensuring compliance while collaborating with cross-functional teams across N...

Lead the charge in regulatory affairs for a multi-facility 3PL organization. Drive compliance initiatives across licensure, trade, and supply chain operations, ensuring risk management and governance...

Lead the charge in regulatory affairs, managing compliance and risk for multiple pharmaceutical programs. Drive strategy, develop controls, and collaborate across teams to ensure adherence to regulati...

Take ownership of regulatory affairs strategy, ensuring compliance and governance across multiple facilities in a dynamic 3PL organization. Lead a team, manage risks, influence stakeholders, and drive...