Regulatory Affairs Specialist Jobs in North Wales, PA

Lead end-to-end GCP audits globally, ensuring compliance and driving improvements in clinical studies. Collaborate with stakeholders to interpret regulations and support regulatory inspections in a dy...

Lead the charge in quality assurance projects, ensuring compliance and timely delivery. Collaborate with cross-functional teams to manage risks, track progress, and drive success through effective com...

Champion compliance initiatives by conducting research, analyzing trends, and collaborating with teams to ensure accurate and effective regulatory responses. Leverage data-driven insights to support c...

Analyze and drive regulatory CMC strategies for investigational and commercial products, collaborating with cross-functional teams to ensure compliance and success in a dynamic biotech environment. Yo...

Lead the charge in optimizing clinical trial operations, ensuring compliance and data integrity across multiple sites. Collaborate with investigators and cross-functional teams to enhance trial qualit...

Champion global regulatory compliance and product stewardship initiatives, ensuring safe manufacturing and distribution while collaborating across departments to meet environmental and chemical regula...

Lead the site sterility assurance program, optimizing compliance with regulations and manufacturing best practices, while collaborating cross-functionally to protect product quality and patient safety...

Drive regulatory compliance initiatives by leveraging SAP EH&S expertise, ensuring safety data accuracy, and engaging in cross-functional teamwork to support product stewardship throughout the lifecyc...

Drive quality assurance success by managing document control processes and ensuring compliance with regulatory standards. Collaborate across teams to maintain accuracy in quality systems while support...

Manage regulatory submissions and compliance for medical devices. Collaborate across departments to ensure adherence to standards, support audits, and maintain quality throughout clinical processes an...

Lead the charge in compliance strategy for U.S. Commercial and Market Access. Collaborate with senior leaders to guide complex compliance issues, manage risks, and support innovative business objectiv...

Elevate clinical outcomes by serving as the key pharmacist liaison among partners, translating real-world issues into actionable insights, driving resolution of clinical concerns, and enhancing produc...

Join a dedicated team driving EHS excellence in the pharmaceutical sector by managing environmental compliance and ensuring adherence to air quality regulations while fostering a culture of sustainabi...

Join a team that's shaping healthcare through innovative legal counsel. You'll oversee commercial contracting, guide compliance, and streamline legal operations for critical partnerships in health sys...

Accelerate regulatory strategy development for oncology products, leading global initiatives to secure IND/CTA approvals and marketing applications. Collaborate with cross-functional teams to navigate...

Lead global strategy for Notified Body engagement, ensuring compliance, managing audits, and driving certification readiness across various jurisdictions. Guide integration assessments, enhance proces...

Champion regulatory compliance by overseeing GXP applications and ensuring effective validation processes within high-stakes global pharmaceutical environments while leading diverse teams with minimal...

Unlock your potential by overseeing site management and monitoring for clinical trials, ensuring compliance with regulations and enhancing site relationships to drive quality and timely delivery of cl...

Collaborate with clients and teams to manage projects, expectations, and delivery, ensuring high standards and strategic growth in a fast-paced medical affairs environment. Leverage experience to iden...

Grow your career with a proactive role ensuring quality standards, leading CAPA initiatives, and driving continuous improvement in a dynamic environment. Leverage your experience to impact product qua...

Join a team that's dedicated to maintaining Good Clinical Practice and human subject protection. Oversee site monitoring, ensure compliance, and support clinical studies through effective communicatio...

Unlock potential by providing strategic CMC regulatory expertise to accelerate the development and lifecycle management of drug-device combination products, ensuring compliance with global regulations...

Elevate your career as a Principal Scientist in CMC Regulatory Affairs, leading strategies for drug-device combination products, guiding cross-functional teams, and ensuring compliance with global reg...

Shape regulatory strategies for drug-device combination products, ensuring compliance with global standards while collaborating across teams to support development and lifecycle management in a hybrid...

Join a team that's committed to driving innovation in regulatory science for drug-device combination products, collaborating cross-functionally to develop and execute strategies for successful global...