Regulatory Affairs Specialist Jobs

Lead the charge in regulatory affairs for a multi-facility 3PL organization. Drive compliance initiatives across licensure, trade, and supply chain operations, ensuring risk management and governance...

Lead the charge in regulatory affairs, managing compliance and risk for multiple pharmaceutical programs. Drive strategy, develop controls, and collaborate across teams to ensure adherence to regulati...

Take ownership of regulatory affairs strategy, ensuring compliance and governance across multiple facilities in a dynamic 3PL organization. Lead a team, manage risks, influence stakeholders, and drive...

Lead regulatory excellence by establishing strategy and governance for multi-facility programs in licensure, compliance, and security while driving sustainable growth and ensuring operational integrit...

Accelerate progress at the forefront of regulatory compliance by leading strategic initiatives, guiding cross-functional teams, and ensuring adherence to complex regulations while fostering a culture...

Elevate the regulatory landscape by guiding strategic promotional communications for Oncology products. Shape impactful messaging while ensuring compliance and aligning with evolving regulations and F...

Shape compliance strategies across hardware and biotech sectors, ensuring products meet global regulatory standards and collaborating with cross-functional teams to drive innovative solutions and main...

Join a team that's enhancing compliance and ethics programs globally. In this role, you will support investigations, manage compliance operations, and drive process improvements while collaborating wi...

Champion CMC regulatory submissions by authoring high-quality dossiers for radiopharmaceuticals and biopharmaceuticals, ensuring compliance and collaboration across teams throughout the product lifecy...

Lead the charge in regulatory strategy development and execution, ensuring compliance for medical devices and pharmaceuticals. Collaborate across teams while advising leadership on regulatory risk and...

Accelerate progress at the intersection of science and compliance, driving regulatory writing excellence for complex submissions while collaborating cross-functionally to ensure quality and timeliness...

Lead the charge in global regulatory compliance, ensuring safe chemical management, product stewardship, and hazard communication across multiple business units and regions. Collaborate with diverse t...

Support the Quality Management System by reviewing and approving key documentation, ensuring compliance with regulations. Champion best practices in discrepancy reporting and CAPA processes while coll...

Unlock potential by driving global regulatory strategies and quality systems, ensuring compliance and market access for medical devices while guiding cross-functional teams in a collaborative environm...

Join a team that's dedicated to ensuring global regulatory compliance and enhancing quality management. Contribute to medical device approvals and improve processes while gaining ownership of quality...

Unlock global regulatory compliance efforts while enhancing the Quality Management System, leading to market access and continuous improvement initiatives. Collaborate cross-functionally to support re...

Contribute to global regulatory compliance while enhancing the Quality Management System. This role offers growth opportunities for an adept regulatory professional to oversee emerging markets and col...

Lead environmental permitting and compliance strategies, ensuring interdisciplinary project execution for a diverse range of clients across the Mid-Atlantic. Utilize technical expertise to manage regu...

Shape the future of environmental compliance by leading regulatory strategies, executing permitting processes, and mentoring staff on diverse projects in the Mid-Atlantic region to meet innovative cli...

Lead NERC CIP compliance initiatives, ensuring audit readiness and cross-functional collaboration. Drive modernization and improvement efforts to safeguard regulatory performance in transmission and d...

Elevate regulatory standards by serving as a senior SME for military-focused drugs and medical devices. Lead the development of submission strategies and mentor cross-functional teams in compliance pr...

Champion regulatory excellence by managing eCTD submissions and ensuring compliance with FDA requirements. Collaborate across teams to maintain documentation standards and training while upholding the...

Transform global regulatory strategies for CMC in Cell & Gene Therapy. Lead a team of experts, ensuring compliance with international regulations. Collaborate cross-functionally and drive successful p...

Explore an impactful leadership role managing global CMC RA teams, ensuring compliance and strategic direction for Cell & Gene Therapy products throughout their lifecycle, while fostering collaboratio...

Lead the charge in global CMC regulatory strategy for Cell & Gene Therapy, ensuring compliance across development, registration, and lifecycle management. Oversee regulatory submissions and provide st...