Senior Regulatory Affairs Specialist Jobs in Mahwah, NJ

Drive innovation as a leader in regulatory data governance, overseeing a global team to ensure high-quality data aligns with strategic business goals while fostering cross-functional collaboration and...

Innovate regulatory strategies to accelerate product development, ensuring compliance and market readiness through expert guidance and cross-functional collaboration, while managing risks and opportun...

Drive global regulatory strategies for pharmaceutical development programs, ensuring compliance and effective submissions. Lead cross-functional teams and navigate complex regulatory landscapes to ach...

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...

Shape the future of patient access by leading regulatory strategies that empower pharmaceutical and biotechnology sponsors to explore innovative pathways and solutions for investigational therapies, e...

Join a team that's dedicated to advancing clinical trials and ensuring smooth study operations by collaborating across functions, supporting trial execution, and maintaining strong communication with...

Lead the charge in supporting clinical study teams with administrative and technical expertise, ensuring trials progress efficiently from activation through close-out while fostering collaboration acr...

Unlock potential by providing essential technical and administrative support for clinical trials, ensuring timely execution from activation to close-out while collaborating with diverse teams and mana...

Champion regulatory excellence by overseeing compliance and managing the Regulatory Affairs team. Drive strategies for clinical operations while ensuring adherence to FDA guidelines and GCP standards...

Accelerate clinical trial success by optimizing monitoring strategies and processes for efficient, quality data management in alignment with regulatory standards and timelines...

Elevate sterility assurance and contamination control strategies globally. Lead risk assessments and foster best practices across our sterile manufacturing sites while championing continuous improveme...

Join a team that's shaping the future of global regulatory strategy. Your expertise will drive compliance, oversee submissions, and lead a dynamic regulatory team in executing key strategies for produ...

Take ownership of regulatory affairs operations, leading teams to enhance processes within clinical trials while ensuring compliance with regulations and fostering collaboration across departments...

Champion the administration and optimization of laboratory systems, ensuring seamless deployment, validation, and integration of informatics solutions within a GMP environment to enhance data integrit...

Manage clinical studies to ensure compliance with regulations and human subject protection. Coordinate site monitoring and maintain quality standards while communicating effectively with site teams to...

Deliver end-to-end bioprocess solutions by leveraging deep expertise in biopharmaceutical workflows, guiding complex customer collaborations, and driving high-impact project leadership for long-term s...

Join a team that's advancing nuclear engineering through component qualification, structural analysis, and seismic qualification for new and existing facilities. Collaborate with multidisciplinary exp...

Transform global regulatory processes by leading approvals, strategizing submissions, and ensuring compliance for medical devices across diverse markets while collaborating with teams and serving as a...

Manage global regulatory strategies for clinical and commercial product registrations. Ensure compliance and successful market access for the PSMA franchise. Lead cross-functional collaborations and d...

Lead the charge in ensuring top-notch inspection readiness across teams, managing quality metrics and overseeing audits. Drive continuous improvement and cultivate accountability within a dynamic phar...

Transform the quality management landscape by leading audits, managing cross-functional teams, and ensuring compliance with global regulations. Drive continuous improvement in quality processes and me...

Take ownership of driving revenue growth and market share through strategic account management and consultative selling in the histology consumables sector, cultivating relationships with laboratory a...

Drive impactful marketing campaigns through creative oversight and strategic management. Collaborate with cross-functional teams to enhance digital initiatives, optimize performance, and support organ...

Engage as a key Quality and Compliance expert across drug/device lifecycles, ensuring adherence to regulations. Collaborate with diverse teams to lead initiatives, manage risks, and uphold data integr...

Develop and validate statistical programs for clinical data analysis, collaborating with cross-functional teams to produce high-quality outputs that adhere to industry and regulatory standards through...