Regulatory Affairs Specialist Jobs in Princeton, NJ

Elevate regulatory standards by coordinating global submissions for medical devices, ensuring compliance with U.S. and international guidelines while supporting cross-functional collaboration and stra...

Join a dynamic team to provide comprehensive regulatory support across clinical, submission, and post-approval phases for pharmaceutical products, ensuring compliance with global regulations while man...

Join a dynamic team to drive compliance and regulatory submissions for medical devices in North America, ensuring adherence to FDA and Health Canada standards while collaborating cross-functionally to...

Join a team that's committed to ensuring compliance with regulatory standards by managing product development and labeling processes. Collaborate with cross-functional teams to navigate regulatory lan...

Lead the charge in optimizing global regulatory affairs by supporting critical business operations and enhancing user experience through effective documentation, training, and change management, ensur...

Advance regulatory compliance as a key member of a collaborative team, ensuring timely solutions for product registration and commercialization. Solve complex challenges and foster innovation while sa...

Drive regulatory CMC strategies and submissions for generic drugs, ensuring compliance with FDA regulations. Collaborate with cross-functional teams to facilitate timely approvals throughout the produ...

Shape the future of medical devices through regulatory expertise, ensuring compliance with local and global standards while collaborating across departments to drive product changes and marketing inte...

Join a dynamic team as you drive regulatory strategies and ensure compliance in post-approval activities for CMC processes. Collaborate cross-functionally, influencing clinical outcomes and advancing...

Empower global labeling excellence by managing regulatory compliance, overseeing document governance, and collaborating with cross-functional teams to ensure safe and effective use of innovative medic...

Contribute to regulatory compliance by reviewing promotional materials, guiding marketing strategy, and ensuring alignment with FDA guidelines. You'll collaborate across teams to promote effective str...

Manage the creation and publishing of regulatory documents to ensure compliance with Health Authority requirements while coordinating eCTD modules and advising on best practices in document management...

Champion regulatory CMC strategies to elevate cell and gene therapies. Drive cross-functional collaborations, oversee global submissions, and ensure compliance. Lead efforts to mitigate risks and supp...

Contribute to compliance training programs by designing effective learning solutions that meet QMS requirements, regulatory standards, and business needs. Collaborate with stakeholders to assess gaps...

Advance your career by overseeing compliance training programs that ensure adherence to regulatory standards. Collaborate with SMEs to create effective learning solutions in a dynamic environment, dri...

Lead regulatory intelligence efforts to ensure compliance and strategic insight within the pharmaceutical landscape. Collaborate across teams to monitor global regulatory changes and support the devel...

Join a team that's shaping the future of global regulatory affairs. You will lead compliance strategies for investigational products and marketing applications through effective submissions and collab...

Accelerate progress at the forefront of regulatory affairs, leading CMC strategy and submissions for development and post-approval programs across the EMEA region. Collaborate cross-functionally to en...

Grow your career with a key Medical Affairs role, providing scientific and clinical support while collaborating cross-functionally to enhance the Tissue Reconstruction portfolio, ensuring medical accu...

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...

Lead the development of regulatory strategies, ensuring compliance while facilitating submissions for clinical trials and marketing authorizations. Collaborate with cross-functional teams to navigate...

Join a team that's dedicated to ensuring compliance in promotional activities for CNS treatments while navigating regulatory pathways in a fast-paced environment. Help shape communications, drive stra...

Empower regulatory excellence by managing promotional materials compliance across global markets, ensuring adherence to laws and internal policies, while aligning with strategic business objectives in...

Champion global regulatory strategies by leading diverse teams in navigating complex approval processes for medical devices. Drive compliance and ensure optimal product launch pathways while addressin...

Take ownership of CMC regulatory strategies, ensuring compliance and driving product development by collaborating across teams and engaging with regulatory authorities to support key initiatives and s...