Regulatory Affairs Manager Jobs in Waltham, MA

Pioneer innovative regulatory strategies and ensure compliance for new products throughout their lifecycle, collaborating closely with teams and health authorities to meet corporate goals and enhance...

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 global regulatory strategies for a diverse medical device portfolio, ensuring compliance and market access across regions. Lead cross-functional teams while influencing product lifecycle and e...

Shape the future of medical devices by leading regulatory strategies, ensuring compliance across global markets, and mentoring a dedicated team. Empower innovation through effective communication with...

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...

Engage with cross-functional teams to ensure regulatory compliance for Expanded Access Programs. Drive essential strategies and submissions while staying aligned with global legislation, impacting pat...

Join a team that's shaping the future of drug development by driving innovative regulatory strategies to ensure compliance with global health authority guidelines and supporting the advancement of tra...

Shape the regulatory landscape by managing submissions from planning to approval, collaborating with cross-functional teams to mitigate risks and ensure compliance while driving project success in a d...

Unlock potential by leading regulatory strategies for CMC products, ensuring compliance and effective submissions while fostering collaboration across teams and Health Authorities to support patient-f...

Oversee innovative regulatory strategies to support transformative clinical programs. Collaborate with cross-functional teams to ensure the preparation of high-quality regulatory submissions while dri...

Champion innovative regulatory strategies for biopharma products, driving compliance and collaboration across teams to advance therapeutic development and ensure successful market entry...

Take ownership of QA operations in radiopharmaceutical manufacturing, ensuring cGMP compliance, conducting audits, resolving quality events, and fostering a culture of continuous improvement within cr...

Drive quality assurance for new product introductions in pharmaceuticals. Leverage leadership skills, manage cross-functional teams, and ensure regulatory compliance to deliver high-quality products e...

Drive regulatory compliance and oversee submissions for innovative medical devices. Lead a team in strategic regulatory guidance, ensuring optimal support for product launches while acting as a liaiso...

Shape the future of regulatory strategy by leading projects that ensure compliance and market access. Drive collaboration across teams while managing processes for development and post-approval phases...

Contribute to regulatory strategy by guiding cross-functional teams through product development, ensuring compliance with regulatory requirements for medical devices and AI technologies while facilita...

Contribute to global compliance efforts by supporting regulatory strategies, preparing submissions, and coordinating with cross-functional teams to ensure adherence to international standards in a dyn...

Lead the charge in transforming global regulatory strategies into successful outcomes. Oversee regulatory activities and empower teams to ensure quality compliance, timely delivery, and robust cross-f...

Deliver impactful CMC regulatory support for IND/CTA development and maintenance, ensuring compliance and completeness across submissions while leading cross-functional collaboration and strategically...

Lead cross-functional teams to navigate regulatory pathways, ensuring alignment with health authorities for timely product delivery. Collaborate to foster strategic relationships, manage submissions...

Drive regulatory excellence by ensuring compliance for product submissions and collaborating across teams to support marketed products and development programs while fostering high performance and inn...

Join our dynamic team to lead international regulatory submissions for innovative digital health technologies, ensuring compliance across global markets and collaborating cross-functionally for succes...

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...

Empower program success by leading quality assurance, compliance, and internal audits. Drive continuous improvement initiatives and ensure all deliverables meet the highest standards in a complex fede...

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