Regulatory Affairs Manager Jobs in Wilmington, DE

Drive global regulatory strategy for medical imaging products, ensuring compliance across the software development lifecycle. Lead a dynamic team, engaging with cross-functional partners and regulator...

Shape the future of medical devices by leading regulatory strategies, ensuring compliance across global markets, and mentoring a dedicated team. Empower innovation through effective communication with...

Engage with cross-functional teams to ensure regulatory compliance for Expanded Access Programs. Drive essential strategies and submissions while staying aligned with global legislation, impacting pat...

Transform the regulatory landscape by shaping product communications and ensuring compliance with FDA regulations. Guide promotional reviews, mentor team members, and navigate evolving regulatory chal...

Unlock potential by leading regulatory CMC submissions and strategies for drug development, ensuring compliance and quality of submissions for small molecules and biologics from inception through post...

Join a dynamic team and lead regulatory strategies for in vitro diagnostics, ensuring compliance and successful submissions while collaborating cross-functionally. Manage project timelines and mentor...

Drive quality assurance for new product introductions in pharmaceuticals. Leverage leadership skills, manage cross-functional teams, and ensure regulatory compliance to deliver high-quality products e...

Shape the future of regulatory affairs by driving strategies for late-stage development programs. Collaborate across teams to ensure compliance, manage submissions, and support critical milestones in...

Pioneer regulatory excellence by leading a team focused on strategic guidance and submissions to optimize product launches in the dynamic medical device landscape. Drive compliance and innovation whil...

Shape the future of regulatory strategy by leading projects that ensure compliance and market access. Drive collaboration across teams while managing processes for development and post-approval phases...

Pioneer regulatory strategies for medical devices, ensuring timely global approvals, compliance, and quality. Collaborate across teams, mentor peers, and tackle complex submissions for US, EU, and bey...

Optimize CMC regulatory strategies for biologic products across the product lifecycle. Lead cross-functional teams to ensure compliance with global regulatory standards while driving successful submis...

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...

Accelerate progress at the intersection of regulatory compliance and innovation. Engage with R&D to drive safe animal nutrition solutions while managing U.S. and Canadian regulatory submissions and do...

Deliver impactful CMC regulatory support for IND/CTA development and maintenance, ensuring compliance and completeness across submissions while leading cross-functional collaboration and strategically...

Accelerate regional regulatory strategies by leveraging expertise to achieve timely, patient-centered product approvals. Collaborate effectively with global teams to ensure compliance and positive hea...

Champion regulatory strategies and submissions for global medical products, ensuring compliance across major markets while leading cross-functional teams and driving process improvements in a collabor...

Lead the charge in developing and overseeing global product labeling strategies for Neuromodulation therapies, ensuring compliance with regulatory standards, and fostering cross-functional collaborati...

Elevate your career by leading global regulatory labeling strategies and initiatives. Oversee labeling governance, ensure compliance, and collaborate with cross-functional teams to support effective p...

Provide comprehensive Regulatory Affairs support to ensure full compliance with U.S. FDA medical device regulations and international standards, facilitating product submissions and ongoing industry c...

Join a dynamic team to facilitate regulatory document preparation and submission, ensuring compliance as you support U.S. regulatory activities and collaborate with cross-functional teams to execute s...

Elevate your career as you ensure regulatory compliance in product development and manufacturing. Collaborate with project teams and guide submissions to domestic and international agencies while main...

Champion regulatory excellence by developing strategies and ensuring effective global registrations for medical devices, while mentoring team members and maintaining compliance with industry standards...

Join our dynamic team as you implement regulatory strategies across multiple therapeutic areas. Collaborate globally, lead project teams, and drive regulatory submissions, ensuring compliance while wo...

Empower global product strategy in Regulatory Affairs, leading teams to navigate complex regulations for therapeutic developments in inflammation and rare diseases. Drive global registration and lifec...