Regulatory Affairs Manager Jobs in Somerset, NJ

Unlock potential by providing strategic CMC regulatory expertise to accelerate the development and lifecycle management of drug-device combination products, ensuring compliance with global regulations...

Elevate your career as a Principal Scientist in CMC Regulatory Affairs, leading strategies for drug-device combination products, guiding cross-functional teams, and ensuring compliance with global reg...

Shape regulatory strategies for drug-device combination products, ensuring compliance with global standards while collaborating across teams to support development and lifecycle management in a hybrid...

Join a team that's committed to driving innovation in regulatory science for drug-device combination products, collaborating cross-functionally to develop and execute strategies for successful global...

Join a team that's transforming life science marketing through strategic ABM campaigns, innovative product launches, and impactful sales enablement initiatives. Collaborate across functions to drive c...

Lead the management of clinical trials from design to execution, ensuring alignment with study protocols, overseeing site operations, and guiding research teams to deliver impactful non-invasive molec...

Take ownership of project management tasks, coordinating client relationships and ensuring successful delivery from inception to completion in a dynamic, supportive environment...

Oversee promotional material reviews and ensure regulatory compliance in the pharmaceutical sector. Collaborate with cross-functional teams to align business objectives with FDA regulations, driving i...

Unlock your potential as you lead outsourcing strategies for pharmacovigilance operations, managing a multi-million-dollar budget while fostering innovative solutions in a dynamic remote environment...

Unlock potential by navigating the complexities of U.S. packaging EPR regulations. Lead educational initiatives, convert dense regulations into actionable guidance, and support industry engagement as...

Support global regulatory CMC strategies for diverse therapeutic areas. Collaborate with multidisciplinary teams to address regulatory assessments and submissions, ensuring compliance throughout the p...

Unlock the potential of global regulatory strategies by leading cross-functional teams to ensure compliance for CMC submissions throughout product lifecycles. Drive innovation and influence outcomes i...

Lead regulatory CMC strategies for product development, ensuring compliance, guiding teams, and interfacing with stakeholders on complex submissions across drug lifecycles...

Join a team that provides critical QA oversight in cell therapy manufacturing, ensuring compliance and quality at every step. Lead QA operations, support manufacturing processes, and drive continuous...

Lead and manage a global Pharmacovigilance audit program, ensuring compliance with regulations and industry best practices. Collaborate with cross-functional teams to enhance processes and drive conti...

Join a team that's dedicated to advancing clinical studies by providing leadership and operational expertise to cross-functional teams, ensuring effective management throughout all phases of clinical...

Lead the enhancement and compliance of the Quality Management System (QMS) for medical devices, ensuring alignment with ISO 13485 and FDA regulations. Manage audits, internal processes, and cross-func...

Shape the future of supply chain by leading cross-functional efforts to optimize manufacturing collaboration, ensuring timely product availability and enhancing planning processes to meet business obj...

Drive EHS initiatives to enhance safety compliance, minimize risks, and promote a positive culture. Lead program management and ensure regulatory adherence while collaborating with personnel to implem...

Lead the charge in optimizing supplier relationships and driving procurement strategies to maximize value and ensure seamless product availability while promoting innovative solutions across diverse s...

Accelerate regulatory strategy development for oncology products, leading global initiatives to secure IND/CTA approvals and marketing applications. Collaborate with cross-functional teams to navigate...

Join a team that's committed to enhancing quality and safety across multiple facilities. This role involves driving compliance, leading improvement initiatives, and collaborating with various stakehol...

Champion scientific strategy and claims substantiation in the dietary supplement sector, leading a team to drive innovation and cross-functional collaboration while engaging with key stakeholders and...

Lead the charge in advancing scientific strategy for our dietary supplement portfolio, guiding evidence generation and stakeholder engagement while managing a team of Medical Affairs professionals to...

Elevate consumer safety through strategic oversight of R&D innovation, ensuring safety objectives align with product vigilance for medium to high-risk consumer healthcare products while mentoring a sk...