Regulatory Affairs Specialist Jobs in Raleigh, NC

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...

Shape the future of drug development by leading nonclinical regulatory strategies and engagements. Collaborate with multidisciplinary teams and clients to drive clinical progress, ensuring compliance...

Elevate your expertise by joining a dynamic team that drives nonclinical regulatory strategies for drug, biologic, and vaccine development, ensuring advancement from discovery to clinical approval whi...

Lead the charge in developing strategic nonclinical regulatory pathways that accelerate medical product advancements, partner with multidisciplinary teams, and navigate complex regulatory landscapes t...

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...

Join a team that shapes global regulatory strategy in a fast-paced environment. You will lead comprehensive regulatory plans, ensuring alignment and execution from development to post-marketing, impac...

Elevate compliance and risk management in FDA-regulated clinical research through expert leadership and quality oversight across clinical trials, ensuring effective protocols and inspection readiness...

Provide regulatory expertise by preparing submissions, ensuring compliance, and collaborating with teams to maintain quality guidelines, supporting product development efforts and compliance with glob...

Drive regulatory excellence by managing submissions, guiding teams, and ensuring compliance. Utilize your expertise to support global projects and foster collaboration in a fast-paced environment focu...

Lead the charge in global regulatory strategies for innovative medical devices, driving project success from registration to compliance. Collaborate across teams to enhance healthcare technologies and...

Join a team that manages site activation processes, ensuring compliance with regulations and SOPs. Collaborate with project teams to maintain timelines, oversee deliverables, and provide expert guidan...

Join a team dedicated to ensuring drug quality compliance by performing data integrity audits, assessing adherence to FDA standards, and providing actionable recommendations to enhance regulatory deci...

Collaborate with cross-functional teams to drive regulatory strategies and manage submissions for drug products. Provide expert guidance to ensure compliance and oversee regulatory activities througho...

Engage with a dynamic team to facilitate regulatory operations for novel therapeutics. Drive submissions to FDA/CVM while collaborating across multidisciplinary teams to set new regulatory standards i...

Take ownership of QA and compliance systems, driving continuous improvement and regulatory adherence through audits, product reviews, and cross-functional collaboration within the site to ensure inspe...

Engage with regulatory authorities as you oversee the process of acquiring and maintaining essential pesticide registrations. Collaborate with cross-functional teams to ensure compliance and drive inn...

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

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

Join our team to lead regulatory strategies across major programs, driving impactful submissions and fostering collaboration within a challenging and dynamic environment. Embrace the opportunity to in...

Join a team that's dedicated to advancing regulatory strategies for innovative SaMD products. Collaborate cross-functionally to drive compliance, manage documentation, and ensure readiness for audits...

Shape the future of quality assurance in manufacturing by ensuring compliance with regulatory standards, conducting audits, mentoring teams, and driving continuous improvement initiatives in a complex...

Unlock potential by leading regulatory CMC strategies for oncology products, coordinating submissions, and collaborating across teams to ensure compliance and successful product registration in a dyna...

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 the charge in ensuring quality compliance during aseptic manufacturing operations. Collaborate with cross-functional teams to maintain high standards of regulatory adherence while supporting life...

Manage and lead comprehensive validation activities in a GMP environment, ensuring compliance with FDA and EMA standards. Collaborate with cross-functional teams while mentoring junior staff and maint...