Regulatory Affairs Manager Jobs in Jersey City, NJ

Lead regulatory compliance programs ensuring inspection readiness and proactive risk management across cross-functional teams. Monitor compliance health, manage data quality, and drive improvements al...

Unlock quality excellence in global clinical trials by leading risk-based management strategies. Collaborate across teams to ensure compliance and enhance processes, making a meaningful impact in pati...

Collaborate with cross-functional teams to oversee regulatory activities for a portfolio of Pharmaceutical Diagnostics products, ensuring compliance and strategic alignment with global standards throu...

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

Reimagine global compliance strategies as you guide regulatory submissions, assess product impacts, and collaborate across teams to ensure adherence to medical device regulations while enhancing quali...

Elevate your career in Global Regulatory Affairs by supporting drug development across various therapeutic areas. Join a dynamic team and gain hands-on experience while navigating regulatory challenge...

Drive digital transformation in Regulatory CMC by leveraging AI and innovative tools to enhance workflows. Collaborate across teams to implement solutions that improve efficiency and foster a culture...

Shape the future of Regulatory CMC with innovative AI solutions, enhancing workflows through digital transformation. Collaborate across teams for greater productivity and operational excellence in a f...

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...

Drive regulatory excellence by leading pre-/post-market activities for medical devices, developing strategies, performing assessments, and coordinating submissions for successful product lifecycle man...

Optimize regulatory strategies and compliance globally by leading cross-functional projects, guiding teams, and liaising with health authorities throughout the drug development lifecycle to ensure suc...

Lead crucial global regulatory strategy in ophthalmology programs while managing a high-performing team. Ensure compliance, drive efficiency, and represent the organization across health authorities t...

Help us shape the future of regulatory affairs by leading a talented team to ensure compliance with advertising and promotion regulations in the immunology sector, influencing industry standards while...

Lead the charge in ensuring compliance for sterile and OSD manufacturing processes by managing batch reviews, documentation, and investigations, while training staff and participating in regulatory in...

Manage regulatory submissions and compliance for medical devices. Collaborate across departments to ensure adherence to standards, support audits, and maintain quality throughout clinical processes an...

Champion regulatory initiatives for in vitro diagnostics, guiding submissions and strategy globally. Foster cross-functional collaboration to drive compliance and product approval while enhancing safe...

Transform regulatory writing by leading complex submissions, mentoring teams, and ensuring compliance. Drive innovation and improve processes while collaborating across teams to enhance product succes...

Inspire global regulatory affairs leadership in CMC for large molecules. Drive innovative strategies, manage compliance, and engage health authorities, ensuring successful product development and life...

Lead the development and execution of global CMC regulatory strategies to support clinical asset advancement. Collaborate cross-functionally to ensure timely, high-quality submissions and health autho...

Drive regulatory strategy by collaborating cross-functionally to influence promotional activities, ensuring compliance while optimizing risk management for impactful business decisions across a dedica...

Drive global regulatory labeling initiatives, ensuring compliance and quality of documentation across diverse markets. Lead strategic governance, influence policies, and collaborate cross-functionally...

Lead global regulatory strategies for oncology programs, ensuring compliance and effectively interacting with regulatory agencies for product approvals in late-stage development...

Join a dynamic team to drive regulatory strategies for products in the US and Canada, ensuring compliance with evolving regulations, and collaborating across functions to support successful product co...

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...

Optimize regulatory strategies for robotic surgical instruments, ensuring compliance and market access. Lead cross-functional teams, prepare vital submissions, and drive innovative product development...