Senior Regulatory Affairs Specialist Jobs in Mansfield, MA

Drive product quality and customer confidence by leading a team in quality investigations and continuous improvement initiatives, while fostering collaboration and accountability across functions to a...

Advance global regulatory strategy for autoimmune programs, guiding cross-functional teams through FDA, EMA, and critical agency interactions. Lead submissions, maintain regulatory timelines, and ensu...

Transform your career by leading validation projects that ensure compliance and innovation within a supportive team. Drive technical strategies, engage in cross-functional collaboration, and deliver s...

Join a team that drives excellence in hardware design integrity through effective collaboration, managing technical data package releases, and ensuring compliance for successful program execution...

Join us to lead capital projects in pharmaceutical manufacturing. Drive project execution from concept to handover while ensuring compliance with quality and safety standards. Collaborate cross-functi...

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

Unlock your potential by coordinating analytical operations and driving process improvements. Collaborate with diverse teams to ensure timely, high-quality data management that supports innovative dru...

Drive regulatory excellence for promotional activities in a dynamic, compliance-focused environment. Lead cross-functional collaboration to ensure alignment with FDA regulations and corporate objectiv...

Partner with us to lead regulatory affairs initiatives, ensuring compliance with FDA advertising guidelines while fostering relationships across departments and driving promotional review processes fo...

Tackle regulatory challenges by ensuring compliance in promotional communications and submissions. Collaborate with cross-functional teams, lead PRC activities, and liaise with the FDA to support stra...

Drive compliance excellence by leading environmental and regulatory initiatives. Partner with senior leaders to implement strategies that minimize risks while ensuring adherence to complex federal, st...

Collaborate with cross-functional teams to lead regulatory writing efforts, ensuring high-quality documentation throughout the drug development lifecycle, from preclinical to registration stages, to s...

Lead the charge in analytical development for radiopharmaceuticals, providing strategic oversight and collaborative support to ensure compliance with GMP and regulatory standards throughout product de...

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...

Lead the charge in ensuring high-quality medical devices by supporting compliance, conducting investigations, and driving process improvements in a dynamic manufacturing environment while enhancing qu...

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

Drive innovation in precursor development, optimizing manufacturing processes while ensuring compliance with regulatory standards to deliver high-quality radiopharmaceutical products for clinical and...

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...

Join a team that's dedicated to enhancing supplier quality in the medical device industry. This role focuses on compliance, audits, and continuous improvement initiatives, playing a vital part in deli...

Shape the future of our global services portfolio, leading the charge in validating life-sciences solutions, enhancing customer outcomes while driving strategy and lifecycle decisions that create comp...

Join a team that drives innovation in nucleic acid operations, optimizing processes from bench to pilot scale. Collaborate cross-functionally to achieve excellence in technology transfer, ensuring suc...

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...

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 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...