Regulatory Affairs Specialist Jobs in Toronto, ON

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...

Join us to lead clinical regulatory activities and team development, ensuring compliance with Health Canada and IRB submissions. Drive project execution, manage resources, and foster a collaborative e...

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...

Engage with cross-functional teams to develop and execute global regulatory CMC strategies for combination devices. Drive compliance and submission processes, ensuring adherence to FDA, EMA, and ICH g...

Empower compliance and audit integrity by supporting internal controls, monitoring processes, and ensuring adherence to regulatory requirements. Join us in maintaining transparency and accuracy in rep...

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...

Manage regulatory compliance programs to ensure institutional safety in research labs. Oversee biosafety and biosecurity efforts, provide expert advice, and collaborate with various agencies to promot...

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...

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...

Grow your career with a dynamic team dedicated to transforming procurement strategies in healthcare. Collaborate globally while enhancing stakeholder value through innovative sourcing, negotiation, an...

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...