Regulatory Affairs Specialist Jobs

Oversee regulatory review of promotional materials for pharmaceutical products. Ensure compliance with FDA regulations while collaborating cross-functionally to support effective advertising strategie...

Transform regulatory strategies for the allergy portfolio, guiding product launches, compliance, and cross-functional collaboration, while mentoring talent and enhancing impact on health and sustainab...

Lead regulatory permitting strategies and ensure compliance with environmental regulations, managing projects from inception to completion while fostering strong client and agency relationships...

Join us to provide regulatory support for global medical device registrations, ensuring compliance and strategy execution. Collaborate with teams and agencies to deliver high-quality documentation whi...

Drive regulatory strategy by guiding product development teams, ensuring compliance, and preparing documentation for global submissions. Monitor regulations and assess their impact, while fostering so...

Champion global regulatory excellence by navigating diverse pathways for safe product registration. Collaborate with cross-functional teams, ensure compliance, and influence international healthcare o...

Transform regulatory strategies by supporting global submissions in oncology, coordinating agency meetings, and collaborating across teams to ensure compliance and drive clinical development goals. Ma...

Drive the advancement of global regulatory submissions in oncology, ensuring compliance for innovative therapeutics through collaborative interactions and strategic planning in a dynamic, science-focu...

Support global regulatory submissions for oncology therapeutics, managing compliance and interactions with agencies. Contribute to cross-functional projects in a fast-paced, innovative environment aim...

Champion regulatory compliance by managing global submissions, ensuring adherence to laws and guidelines. Collaborate across teams to develop strategies, optimize processes, and maintain effective age...

Unlock potential by ensuring compliance with food labeling regulations while collaborating across departments. Lead initiatives, provide expertise in regulatory matters, and mentor team members to uph...

Champion regulatory excellence in a dynamic environment, driving compliance and oversight through effective leadership. Foster relationships, manage audits, and guide the team in enhancing organizatio...

Explore the potential of Tumor Immunotherapy by coordinating clinical trials, ensuring regulatory compliance, and contributing to groundbreaking cancer research initiatives in a collaborative, special...

Lead the charge in ensuring compliance with quality standards and regulations through effective oversight of documentation and daily activities. Collaborate with teams to drive improvements and suppor...

Lead the charge in ensuring compliance with quality standards through oversight of daily activities, documentation control, and cross-functional collaboration to meet regulatory requirements and drive...

Drive human factors and usability engineering while supporting regulatory submissions. Collaborate with cross-functional teams to enhance product safety and compliance in bringing innovative medical t...

Join a team that's dedicated to driving quality improvements and ensuring compliance in biological manufacturing. In this role, you'll manage CAPA, deviations, and quality metrics while supporting cro...

Unlock potential by leading North American regulatory strategies for innovative oncology products. Drive submissions, manage FDA interactions, and ensure compliance across diverse projects, fostering...

Lead the charge in regulatory strategy for ophthalmologic products, ensuring compliance with global standards. Manage submissions, coordinate projects, and oversee promotional materials. Join a dedica...

Transform safety and quality compliance by leading initiatives that ensure GMP adherence and operational excellence in clinical supply manufacturing, working closely with cross-functional teams to dri...

Join a team that's establishing quality assurance systems in a GMP environment, ensuring compliance and excellence in oral solid dosage and sterile drug manufacturing. Help shape a culture of 'Right F...

Shape the future of global product registrations by supporting regulatory teams with Veeva Vault RIM and ensuring system improvements and compliance. Collaborate cross-functionally to resolve issues a...

Unlock potential by ensuring compliance with GMP regulations and quality standards. Collaborate with cross-functional teams to support quality events, tracking metrics, and inspection readiness while...

Engage with us to shape cutting-edge CMC regulatory strategies. Lead impactful submissions and lifecycle activities, collaborating across teams to enhance patient outcomes worldwide. Join a dynamic en...

Drive regulatory compliance and product registrations globally, collaborating with cross-functional teams to navigate complex regulatory landscapes for medical devices and ensure timely market access...