Regulatory Affairs Manager Jobs in Malvern, PA

Reimagine Regulatory Affairs by leading complex outsourcing programs and driving client success. Utilize deep expertise in strategy and operations to manage projects, mentor teams, and deliver tailore...

Lead the charge in ensuring regulatory compliance globally for Expanded Access Programs, enhancing patient access to innovative therapies through collaboration across diverse teams while maintaining q...

Explore an impactful role overseeing regulatory service processes, ensuring compliance and efficiency across operations. Collaborate with teams and clients to deliver high-quality outputs that meet ev...

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...

Innovate and execute regulatory CMC strategies for radiopharmaceutical products, ensuring compliance across global markets. Collaborate with cross-functional teams to support submissions and enhance p...

Partner with us to drive regulatory compliance for innovative medical devices. Support market distribution and global registrations while ensuring adherence to standards, reviewing documentation, and...

Lead the charge in regulatory strategy for clinical studies, providing expert guidance on complex global compliance. Drive communication with health authorities and ensure timely documentation while c...

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...

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...

Lead quality and compliance efforts for a cloud-native software platform. Ensure software development meets FDA regulations and GxP standards while managing validation processes and collaborating with...

Lead the charge in transforming health authority interactions by overseeing the development and continuous improvement of digital solutions that enhance regulatory excellence and streamline operations...

Drive global quality compliance initiatives by leading audits and ensuring regulatory adherence across various facilities and stakeholders. Champion compliance risk identification and resolution while...

Join a team that's shaping regulatory strategies in biopharmaceuticals. This role involves leading regulatory submissions and collaborating across project teams to ensure compliance while advancing co...

Lead strategic Regulatory CMC initiatives for the Cardiovascular portfolio, ensuring compliance and successful product lifecycle management while developing and mentoring a high-performing team of Reg...

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...

Engage as a Global Regulatory Leader, driving innovative regulatory strategies and interactions to streamline product development and global approval processes, while ensuring compliance and effective...

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...

Join a dynamic team where your regulatory expertise will elevate product compliance and drive innovative solutions in the medical device industry. Collaborate cross-functionally to ensure swift approv...

Launch your career by supporting regulatory submissions and compliance activities, coordinating documentation, and engaging in team collaborations to drive successful outcomes in drug development and...

Pioneer regulatory excellence by leading FDA submissions and compliance. Manage the lifecycle of medical product filings, ensuring alignment with evolving regulations across diverse jurisdictions in a...

Drive regulatory project execution for medical devices and combination products, ensuring compliance with global standards while collaborating with cross-functional teams to manage timely submissions...

Elevate regulatory affairs by managing global CMC submissions for biological products. Lead multi-disciplinary teams, assess risks, and ensure timely communication with regulatory agencies to meet dev...

Champion global regulatory activities, ensuring high-quality submissions and strategic partnerships. Support lifecycle management across late-stage development, driving compliance with U.S. and intern...

Champion client success by managing accounts for 20-30 small pharma clients. Leverage IQVIA’s data assets to deliver high satisfaction, drive revenue growth, and facilitate consultative sales while na...

Support regulatory excellence by preparing submissions and documentation for medical devices across global markets, ensuring compliance and timely approvals. Collaborate with product teams to streamli...