Regulatory Affairs Manager Jobs in Raynham, MA

Lead our regulatory operations team in navigating UDI compliance and FDA regulations for medical devices, ensuring accurate registrations and supporting cross-functional initiatives that enhance produ...

Lead regulatory strategies for CMC submissions and compliance in global projects. Collaborate with cross-functional teams to ensure accurate submissions and establish key relationships with authoritie...

Reimagine Regulatory Affairs by leading complex outsourcing programs and driving client success. Utilize deep expertise in strategy and operations to manage projects, mentor teams, and deliver tailore...

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...

Drive regulatory compliance for innovative products by leading global strategies. Collaborate cross-functionally to ensure market readiness and sustain products throughout their lifecycle while mainta...

Unlock your potential as a Senior Manager leading regulatory submissions for biologics. Collaborate across teams, ensuring high-quality documentation for global approvals while navigating complex chal...

Grow your career with a dynamic role guiding global regulatory strategies for biologics, collaborating cross-functionally while ensuring timely submissions and compliance within a fast-paced biotech e...

Lead the charge in regulatory strategy for clinical studies, providing expert guidance on complex global compliance. Drive communication with health authorities and ensure timely documentation while c...

Join a dynamic team and lead regulatory strategies for in vitro diagnostics, ensuring compliance and successful submissions while collaborating cross-functionally. Manage project timelines and mentor...

Transform global regulatory strategies for oncology programs, leading cross-functional teams and ensuring timely submissions and approvals while developing high-caliber regulatory talent...

Transform regional regulatory engagement by leading strategy, fostering relationships, and advocating for efficient electric transmission policies. Collaborate across departments to align regulatory g...

Contribute to regulatory excellence by leading teams to develop successful strategies for biotech and pharmaceutical projects, ensuring compliance with FDA and global agencies while enhancing innovati...

Join a dynamic team to build relationships and drive revenue growth in the Standards sector, focusing on Reference Materials and Analytical Standards. Collaborate with stakeholders to meet sales targe...

Tackle regulatory challenges by overseeing global quality compliance support, including managing audit logistics, controlled documents, training, and CAPA. Ensure adherence to quality standards while...

Champion the GxP Quality Systems by ensuring compliance and effectiveness through improved processes, training initiatives, and rigorous documentation. Engage cross-functional teams to maintain qualit...

Take ownership of U.S. regulatory submissions, ensuring accuracy and compliance with FDA requirements. Collaborate cross-functionally to coordinate IND, NDA, and BLA filings, executing processes withi...

Shape the future of regulatory excellence by managing global submissions, ensuring compliance across the drug development lifecycle, and collaborating across teams to facilitate strong health authorit...

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...

Champion global regulatory activities, ensuring high-quality submissions and strategic partnerships. Support lifecycle management across late-stage development, driving compliance with U.S. and intern...

Shape the future of drug development by leading cross-functional CMC regulatory projects, mentoring talent, and influencing decision-making to ensure compliance and excellence in pharmaceuticals...

Unlock potential by leading regulatory CMC strategies for late-stage small molecule development. Collaborate with cross-functional teams to ensure compliance with global standards while driving qualit...

Lead and manage CQV activities for biopharmaceutical projects, ensuring compliance with cGMP and regulatory standards. Collaborate cross-functionally to oversee project execution, while guiding teams...

Accelerate progress at regulatory advocacy, guiding product compliance, and strategy development. Utilize expertise in scientific, regulatory, and business issues to support global product submissions...

Partner with us to drive regulatory CMC strategies and lead major global submissions in the biopharmaceutical sector. Leverage your expertise to enhance compliance and support product lifecycles throu...

Join a dynamic team in global pharmacovigilance, driving signal management, benefit-risk assessments, and safety surveillance for life-changing therapies. Collaborate cross-functionally to enhance pat...