Regulatory Affairs Specialist Jobs in Mississauga, 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...

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...

Drive regulatory excellence in mRNA therapeutics by leading Canadian strategy and submissions. Foster collaboration, mentor talent, and shape innovative solutions in a rapidly evolving landscape to en...

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...

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 a team that's committed to enhancing regulatory activities for product compliance, guiding cross-functional initiatives, and mentoring junior staff within a dynamic environment focused on medical...

Advance compliance excellence by supporting audit readiness and integrity of financial reporting. Collaborate within a dynamic team to drive adherence to regulatory and internal standards, ensuring tr...

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...

Join us to lead strategic regulatory initiatives for oncology products, guiding successful FDA interactions and submissions while shaping global strategies that advance innovative treatments for patie...

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...

Shape the future of project delivery by leading planning, scheduling, and cost control for diverse engineering projects, ensuring successful outcomes through robust data management and collaboration w...

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...

Optimize medical writing deliverables for research projects ensuring clarity and compliance with regulatory standards. Collaborate across departments to deliver high-quality documents efficiently whil...

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...

Join a team that's dedicated to advancing clinical research by overseeing site management, ensuring compliance, and optimizing project timelines while fostering collaboration among stakeholders to ach...

Elevate product quality and compliance by owning the ISO 13485 system, leading audits, and guiding regulatory strategies, ensuring seamless pathways from development to market for medical devices whil...

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...

Shape the future of regulatory affairs by leading strategies, ensuring compliance with Health Canada, and fostering collaboration to enhance product development and approvals within a dynamic global e...

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...