Regulatory Affairs Manager Jobs in Acton, MA

Lead global regulatory strategies in oncology, ensuring timely approvals and innovative approaches. Collaborate with cross-functional teams, manage risks, and influence stakeholders to deliver life-ch...

Drive regulatory strategy and team coordination for innovative plasma-derived therapies with a focus on compliance and global submissions to enhance patient access and therapeutic advancements...

Champion regulatory strategies and submissions for global medical products, ensuring compliance across major markets while leading cross-functional teams and driving process improvements in a collabor...

Lead the charge in developing and overseeing global product labeling strategies for Neuromodulation therapies, ensuring compliance with regulatory standards, and fostering cross-functional collaborati...

Elevate your career by leading global regulatory labeling strategies and initiatives. Oversee labeling governance, ensure compliance, and collaborate with cross-functional teams to support effective p...

Drive your career by leading global regulatory strategies for complex projects, ensuring compliance, and enhancing patient access to innovative therapies. Collaborate cross-functionally to influence k...

Shape the future of regulatory strategy and execution, driving high-quality submissions and interactions with global health authorities throughout the drug development lifecycle, ensuring adherence to...

Transform regulatory processes by driving global submissions and strategies, collaborating with diverse teams to ensure compliance with health authority standards throughout product lifecycle manageme...

Lead regulatory compliance for medical devices throughout product lifecycles. Collaborate with cross-functional teams to ensure adherence to global regulations and guide technical expertise in submiss...

Provide comprehensive Regulatory Affairs support to ensure full compliance with U.S. FDA medical device regulations and international standards, facilitating product submissions and ongoing industry c...

Contribute to regulatory efforts ensuring compliance and safety in medical devices. Engage with cross-functional teams on submissions and documentation while developing expertise in FDA, EU, and inter...

Drive regulatory compliance and strategy in the medical device sector, leading submission management and overseeing compliance activities. Champion innovative solutions while guiding cross-functional...

Shape global RegCMC strategies for small molecules, ensuring timely regulatory submissions. Collaborate across teams to mitigate risks and advance clinical development in a dynamic biotech environment...

Elevate your career as you ensure regulatory compliance in product development and manufacturing. Collaborate with project teams and guide submissions to domestic and international agencies while main...

Optimize regulatory strategies for advertising and promotion, ensuring compliance with FDA guidance and contributing to cross-functional teams to enhance product messaging and educational materials, w...

Transform relationships into growth by managing a diverse portfolio of global ecommerce merchants. Build strategic partnerships, optimize client experiences, and drive revenue through collaboration an...

Join a team that's shaping global regulatory strategies for innovative medical devices. Leverage your expertise in Software as a Medical Device (SaMD) to make impactful submissions and ensure complian...

Engage in leading GCP audit programs, managing staff development, and implementing quality initiatives to enhance safety compliance. Contribute to a dynamic, science-focused environment dedicated to i...

Lead and empower a team of regulatory compliance experts in supporting a ground-breaking healthcare platform, ensuring regulatory alignment and operational excellence within a complex, evolving enviro...

Join a team that's passionate about advancing regulatory projects in the pharmaceutical industry. Drive compliance and ensure timely submissions while collaborating across functions, developing strate...

Transform U.S. regulatory strategies in Obesity and Related Conditions, ensuring compliance and patient safety. Lead teams on global initiatives and manage key submissions for clinical trials and mark...

Lead the charge in advancing novel gene-based therapies by guiding regulatory CMC strategy. Collaborate with cross-functional teams and external partners to ensure compliance and drive successful subm...

Drive regulatory compliance by developing submissions and strategies for medical devices. Collaborate across teams to ensure timely approvals while adhering to global standards and practices in a dyna...

Manage site-level regulatory operations for clinical trials, ensuring compliance with U.S. regulations. Collaborate with cross-functional teams and provide guidance for regulatory submissions, fosteri...

Lead the charge in shaping regulatory strategies for cardiovascular devices. Collaborate with product teams to ensure compliance, oversee submissions, and mentor junior specialists while driving timel...