Senior Regulatory Affairs Specialist Jobs in Trenton, NJ

Champion regulatory strategies and submissions for global medical products, ensuring compliance across major markets while leading cross-functional teams and driving process improvements in a collabor...

Pioneer regulatory strategies for medical devices, ensuring timely global approvals, compliance, and quality. Collaborate across teams, mentor peers, and tackle complex submissions for US, EU, and bey...

Unlock potential by leading regulatory submissions and ensuring compliance with FDA guidelines. Collaborate across teams to drive projects efficiently while coordinating with vendors. Your expertise w...

Join a team that's shaping global regulatory strategies for innovative medical devices. Leverage your expertise in Software as a Medical Device (SaMD) to make impactful submissions and ensure complian...

Elevate your career as you ensure regulatory compliance in product development and manufacturing. Collaborate with project teams and guide submissions to domestic and international agencies while main...

Drive global regulatory strategy for medical imaging products, ensuring compliance across the software development lifecycle. Lead a dynamic team, engaging with cross-functional partners and regulator...

Shape your career by supporting regulatory compliance for clinical investigations and product distribution worldwide. Contribute to approvals and quality standards in a collaborative environment while...

Join a team that's shaping regulatory strategies in biopharmaceuticals. This role involves leading regulatory submissions and collaborating across project teams to ensure compliance while advancing co...

Lead the charge in regulatory affairs for innovative diagnostics and medical devices. Oversee compliance, manage submissions, and collaborate across teams to ensure successful product market entry and...

Champion regulatory excellence by developing strategies and ensuring effective global registrations for medical devices, while mentoring team members and maintaining compliance with industry standards...

Manage site-level regulatory operations for clinical trials, ensuring compliance with U.S. regulations. Collaborate with cross-functional teams and provide guidance for regulatory submissions, fosteri...

Elevate your career by leading global regulatory labeling strategies and initiatives. Oversee labeling governance, ensure compliance, and collaborate with cross-functional teams to support effective p...

Unlock potential by overseeing regulatory strategies for advertising and promotional materials. Collaborate with cross-functional teams and serve as a key liaison with the FDA to ensure compliance and...

Join a team that's dedicated to enhancing healthcare compliance. This role requires expertise in regulations and standards, managing projects, and fostering team growth while ensuring client facilitie...

Join a dynamic team and lead regulatory strategies for in vitro diagnostics, ensuring compliance and successful submissions while collaborating cross-functionally. Manage project timelines and mentor...

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...

Join a team that's passionate about advancing regulatory projects in the pharmaceutical industry. Drive compliance and ensure timely submissions while collaborating across functions, developing strate...

Engage with cross-functional teams to ensure regulatory compliance for Expanded Access Programs. Drive essential strategies and submissions while staying aligned with global legislation, impacting pat...

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...

Optimize CMC regulatory strategies for biologic products across the product lifecycle. Lead cross-functional teams to ensure compliance with global regulatory standards while driving successful submis...

Lead the charge in overseeing complex regulatory projects, ensuring timely and budget-compliant deliverables while managing teams and fostering compliance through innovative solutions and collaboratio...

Lead the charge in managing complex regulatory projects, ensuring quality compliance and innovative solutions while directing teams to deliver on time and within budget across multiple areas of expert...

Provide comprehensive Regulatory Affairs support to ensure full compliance with U.S. FDA medical device regulations and international standards, facilitating product submissions and ongoing industry c...

Grow your career with a pivotal role leading comprehensive testing strategies for innovative combination products, ensuring quality and compliance throughout the product life cycle, while collaboratin...

Engineer innovative CMC regulatory strategies to ensure compliance across product lifecycles. Collaborate with cross-functional teams to deliver high-quality submissions and expert guidance while main...