Senior Regulatory Affairs Specialist Jobs in West Chester, PA

Strategize global CMC regulatory approaches for innovative therapeutics, bridging research and development. Lead regulatory submissions and guide teams through evolving landscapes, ensuring compliance...

Lead the development and execution of global CMC regulatory strategies to support clinical trials and market applications, ensuring compliance with regulatory requirements throughout the product lifec...

Empower your career by leading global regulatory strategies for medical devices and diagnostics. Collaborate with cross-functional teams to ensure compliance and drive market access while mentoring ot...

Lead the charge in shaping global Regulatory CMC strategies for synthetic moieties in ADCs, ensuring compliance and successful delivery of regulatory milestones across product development and lifecycl...

Champion regulatory excellence by leading cross-functional teams, ensuring compliance, and driving successful oncology drug development through strategic planning and expert guidance...

Manage regulatory activities for advertising and promotion, ensuring compliance while collaborating with cross-functional teams to develop impactful product messaging and materials that align with com...

Unlock your potential as a Global Regulatory Leader, driving regulatory strategy and submissions for CNS projects. Collaborate with cross-functional teams, mentor junior staff, and ensure compliance w...

Shape the future of pharmacovigilance by leading compliance oversight for ICSR reporting. Collaborate with cross-functional teams to identify risks, drive improvements, and ensure adherence to regulat...

Lead the charge in ensuring compliance for ICSR reporting, driving risk management and continuous improvement. Collaborate with cross-functional teams to enhance pharmacovigilance practices and foster...

Lead regulatory compliance programs ensuring inspection readiness and proactive risk management across cross-functional teams. Monitor compliance health, manage data quality, and drive improvements al...

Take ownership of IMP labeling processes, ensuring compliance with global regulations and quality standards while collaborating cross-functionally to support clinical trial timelines and enhance label...

Join a team that's advancing regulatory strategies for drug substance manufacturing. Lead the charge in selecting and justifying Regulatory Starting Materials, ensuring compliance with global guidelin...

Empower regulatory excellence by managing promotional materials compliance across global markets, ensuring adherence to laws and internal policies, while aligning with strategic business objectives in...

Empower your career by leading regulatory advertising initiatives, ensuring compliance while collaborating with cross-functional teams to develop impactful product messaging for marketed and pipeline...

Lead regulatory intelligence efforts, ensuring compliance and strategic guidance across global frameworks, with a focus on containment systems and pharmaceutical operations in a collaborative, fast-pa...

Drive regulatory strategy across major programs, leading high-impact submissions and authority engagement. Collaborate with cross-functional teams to optimize clinical development and ensure complianc...

Unlock potential by leading regulatory compliance for IVD products, ensuring adherence to global standards. Collaborate with cross-functional teams to assess risks, manage adverse events, and drive co...

Join a global team to shape regulatory strategies in biotechnology, supporting product development and lifecycle management in Inflammation and Rare Diseases. Lead regulatory efforts, ensure complianc...

Unlock potential by leading regulatory writing for complex submissions, mentoring junior writers, and driving departmental initiatives. Collaborate with cross-functional teams to ensure compliance and...

Engage in quality operations for externally manufactured pharmaceutical products, managing relationships with CMOs and cross-functional teams. Ensure compliance, oversee batch reviews, and drive conti...

Join a team that's driving innovation in R&D and Regulatory processes. Leverage your Veeva RIM expertise, manage global compliance systems, and implement solutions that meet dynamic business needs whi...

Advance your career by leading clinical research projects and ensuring compliance with timelines and standards. Collaborate with stakeholders and clinical sites to safeguard subjects' rights and data...

Champion quality assurance excellence in GMP for drug substance and products, overseeing compliance and methodologies. Collaborate to ensure regulatory adherence while maintaining operational efficien...

Advance your career in regulatory affairs through a dynamic fellowship program. Collaborate with experts, tackle real-world projects, and gain invaluable insights into drug development while enhancing...

Contribute to global drug development by engaging with health authorities, learning regulatory requirements, and tackling real-world projects. This two-year fellowship offers hands-on experience in re...