Senior Regulatory Affairs Specialist Jobs in Raritan, NJ

Unlock potential by leading global sterility assurance and contamination control initiatives. Drive compliance and best practices across sterile manufacturing sites while fostering cross-site collabor...

Elevate sterility assurance and contamination control strategies globally. Lead risk assessments and foster best practices across our sterile manufacturing sites while championing continuous improveme...

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...

Grow your career with a key role in Quality Assurance for US Navy submarine systems, focusing on quality planning, auditing, and compliance programs while ensuring product integrity and adherence to r...

Join a team that's dedicated to maintaining Good Clinical Practice and human subject protection. Oversee site monitoring, ensure compliance, and support clinical studies through effective communicatio...

Collaborate with clients and teams to manage projects, expectations, and delivery, ensuring high standards and strategic growth in a fast-paced medical affairs environment. Leverage experience to iden...

Lead regulatory support for Neurology and Oncology agents, driving strategies and submissions for global approvals. Collaborate across teams to enhance development timelines and ensure compliance with...

Unlock potential by driving strategic revenue growth in RTSM within global CRO partnerships. As an expert, you'll support sales strategies, potential deals, and amplify Medidata's market presence thro...

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

Help us drive product success in biopharma by managing lifecycle initiatives, collaborating cross-functionally, and supporting growth strategies to enhance profitability and customer satisfaction acro...

Champion regulatory compliance by overseeing GXP applications and ensuring effective validation processes within high-stakes global pharmaceutical environments while leading diverse teams with minimal...

Tackle clinical monitoring challenges while leading site initiatives for quality compliance and protocol adherence. Collaborate with cross-functional teams to ensure successful clinical trial executio...

Elevate your career by leading compliance and quality in clinical trials. Collaborate with teams to ensure protocol adherence, site training, and resolve issues while maintaining high standards of mon...

Optimize your clinical research career by playing a vital role in overseeing and conducting site monitoring for clinical trials, ensuring compliance, quality, and effective team collaboration througho...

Unlock potential by leading site monitoring for clinical trials. Collaborate closely with cross-functional teams to ensure compliance, enhance recruitment, and oversee execution while providing guidan...

Champion the ethical landscape by conducting thorough investigations into compliance issues, mitigating risks, and fostering an integrity-driven culture across the organization through collaboration a...

Help us drive the development of advanced sterile biologics products from early design to commercialization. Collaborate with teams to ensure robust formulations, effective processes, and successful p...

Innovate with us to ensure design quality and compliance for Class II/III medical devices. Collaborate across teams, drive adherence to regulations, and lead quality assurance throughout the product l...

Shape a quality control framework for cancer registrars by conducting audits, providing essential feedback, and ensuring compliance with standards. Collaborate with a dedicated team to enhance data qu...

Transform the biopharmaceutical landscape by advising clients on regulatory compliance and clinical pharmacology strategies, leveraging your expertise to impact innovative drug development across dive...

Lead the global CMC regulatory strategy, driving successful development and submission of biologics. Collaborate cross-functionally to ensure compliance with regulatory requirements and facilitate tim...

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...

Join a team that's focused on shaping US regulatory intelligence and external engagement. Collaborate with experts to interpret developments and provide strategic insights that support informed decisi...

Lead quality assurance efforts in innovative medical device development. Act as a subject matter expert in compliance, design control, and risk management, ensuring product integrity throughout the so...

Join a team that's dedicated to enhancing clinical trial quality through leadership, mentorship, and oversight. Engage remotely with cross-functional teams, driving high standards for patient safety a...