Senior Regulatory Affairs Specialist Jobs in Raritan, NJ

Shape the future of oncology therapeutics by driving global regulatory strategy and enabling fast track approvals for novel drug candidates. Collaborate cross-functionally to ensure compliance with FD...

Manage reimbursement strategies supporting business goals across product areas. Collaborate with teams to guide product development, analyze landscapes, and educate stakeholders on reimbursement impac...

Join a dynamic team to oversee cost management functions, enhance project financial performance, and ensure compliance through accurate forecasting, variance analysis, and reporting to drive strategic...

Join a team that's dedicated to ensuring dietary supplement quality by executing robust QA GMP compliance processes. Your expertise will be pivotal in managing supplier quality and driving continuous...

Elevate your career as a strategic leader in global regulatory affairs, managing clinical and commercial drug product compliance. Collaborate cross-functionally to ensure adherence to regulations and...

Make your mark at the forefront of regulatory strategy! Lead clinical and commercial regulatory initiatives, ensuring compliance while driving successful drug product registrations and global submissi...

Join a dynamic team as you oversee risk management across clinical studies, utilizing expertise in RBQM to enhance participant safety, ensure data reliability, and uphold regulatory compliance through...

Drive supplier quality excellence by managing Quality Technical Agreements (QTAs) and conducting GMP audits. Lead cross-functional collaborations to ensure compliance with regulatory standards while e...

Transform healthcare solutions by leveraging your HL7 expertise to develop programs and processes for innovative data management products while providing critical support and optimizing customer inter...

Champion compliance initiatives by conducting research, analyzing trends, and collaborating with teams to ensure accurate and effective regulatory responses. Leverage data-driven insights to support c...

Drive quality assurance success by managing document control processes and ensuring compliance with regulatory standards. Collaborate across teams to maintain accuracy in quality systems while support...

Lead regulatory teams to shape global registration strategies and ensure compliance. Drive innovative approaches, influence cross-functional initiatives, and support business growth through proactive...

Join an innovative team as a Senior Supplier Quality Engineer, enhancing supplier performance and compliance across global operations. Drive strategic quality initiatives, lead supplier audits, and me...

Join a dynamic team to develop and optimize business rule logic, ensuring alignment with operational goals. Collaborate with multiple departments to identify and resolve technical limitations, fosteri...

Explore opportunities as a Clinical & Regulatory Information Management SME, supporting client delivery across VeevaRIM and Clinical initiatives. Engage with stakeholders, optimize processes, and enha...

Optimize regulatory document management processes by partnering with stakeholders, gathering requirements, and supporting product enhancements to drive continuous improvement and ensure high-quality o...

Drive innovative digital solutions for regulatory operations, enhancing lifecycle and document management. Collaborate cross-functionally to ensure high-quality outcomes while optimizing business proc...

Drive quality assurance in GMP operations, ensuring compliance and product integrity while collaborating with internal and external stakeholders. Contribute to clinical manufacturing excellence throug...

Lead the charge in compliance strategy for U.S. Commercial and Market Access. Collaborate with senior leaders to guide complex compliance issues, manage risks, and support innovative business objectiv...

Shape the future of sterility assurance by developing global standards, leading contamination control strategies, and establishing a Center of Excellence to ensure compliance and foster innovation acr...

Lead regulatory strategy for complex clinical projects, ensuring cohesive integration across global platforms while mentoring teams and managing both internal resources and vendor relationships for op...

Elevate legal strategies by leading commercial contracting initiatives across U.S. and Canada for MedSurg operations. Collaborate with business leaders to navigate complex agreements while ensuring co...

Join a collaborative team to ensure regulatory compliance and business continuity, conducting assessments and submissions in line with FDA guidelines while managing cross-functional projects and datab...

Elevate your career by driving growth strategies across sales, consulting, and product management to enhance executive relationships in the MedTech industry, focusing on Quality, Regulatory, and Compl...

Champion the development of high-quality clinical regulatory documents, ensuring compliance while collaborating on cross-functional teams. Excel in project management and critical thinking to navigate...