Regulatory Affairs Specialist Jobs in Toronto, ON

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...

Champion regulatory excellence by leading a high-performing team in strategic submission oversight and compliance, ensuring timely approvals for a diverse product portfolio across US and Canadian mark...

Lead regulatory strategy by ensuring adherence to provincial and federal laws, while managing compliance risks and overseeing submissions to regulatory bodies. Collaborate with cross-functional teams...

Join a team that's dedicated to ensuring regulatory compliance across functions. Lead submission preparation, provide guidance on protocols, and drive continuous improvement efforts, playing a key rol...

Partner with us to ensure compliance and quality in regulatory submissions for complex injectable products and biosimilars, providing pivotal support and guidance throughout the product development li...

Lead the charge in executing global regulatory CMC strategies for small molecules. Collaborate with cross-functional teams to ensure compliance and contribute to the preparation of regulatory submissi...

Join our team to drive global regulatory CMC strategies for small molecules. You'll manage submissions, collaborate with cross-functional teams, and ensure compliance with global regulatory standards...

Accelerate progress at our organization by leading a diverse team to ensure product safety and compliance across global markets, driving innovation while managing regulatory affairs and toxicology ass...

Lead regulatory submissions for medical devices, ensuring compliance and alignment with commercial strategies. Collaborate with stakeholders on product approval processes while fostering an engaged cu...

Lead the charge in enhancing quality systems and compliance in Life Sciences. Collaborate with teams to implement robust processes, mentor talent, and drive continuous improvements, ensuring a culture...

Architect global compliance strategies for Direct Materials Certification. Lead modernization, streamline processes across Biologics and Molecules, and resolve complex regulatory challenges while ensu...

Drive optimization and support for Veeva Vault and CRM systems within pharmaceutical applications, engaging stakeholders to enhance processes, ensure compliance, and facilitate effective solutions acr...

Help us elevate pharmaceutical quality standards through rigorous compliance, ensuring all product processes from manufacturing to market align with GMP and regulatory requirements. Collaborate with t...

Lead and support a team of regulatory professionals to drive compliance, optimize submission strategies, and ensure successful outcomes for a portfolio of prescription products throughout their lifecy...

Drive critical pharmaceutical CQV projects by leading validation activities. Collaborate with cross-functional teams to ensure compliance with health standards. Use your expertise to troubleshoot and...

Lead the charge in shaping policies and advocating for business needs in complex regulatory environments by managing key stakeholder relationships and developing high-performing teams to drive strateg...

Drive compliance excellence by managing global trade operations, collaborating across teams, and implementing strategies to uphold regulatory standards, facilitating business growth while ensuring leg...

Oversee international trade compliance operations to ensure adherence to regulations. Collaborate with cross-functional teams, manage processes, and implement strategies to support business growth whi...

Join a team that's dedicated to ensuring the highest quality standards for biologic products. This role engages in GMP oversight, collaborates globally with quality teams, and supports regulatory comp...

Shape the future of quality assurance by ensuring compliance and oversight for biologic products. Collaborate with teams to address complex quality issues and support regulatory inspections, maintaini...

The Senior Clinical Research Associate (Sr. CRA) is responsible for managing and monitoring clinical trial sites to ensure patient safety and compliance with regulatory standards. This role involves o...

Empower meaningful change by leading RWE projects, driving client engagement, and enhancing team cohesion while managing proposals and ensuring operational excellence for impactful real-world studies...

Champion innovative real-world evidence projects, lead strategic initiatives, and drive client satisfaction while mentoring a skilled team. Collaborate with business development partners to ensure imp...

Champion regulatory excellence in nuclear licensing processes for advanced projects. Collaborate with cross-functional teams to prepare essential safety documentation and analyze complex engineering d...

Unlock potential by leading global regulatory compliance for medical products, ensuring adherence to safety and environmental standards. Oversee testing, documentation, and audits to meet market requi...