Job Overview
Location
Canada - Toronto
Job Type
Full-time
Category
Product Management
Date Posted
June 16, 2026
Full Job Description
đź“‹ Description
- • Lead a team of Product Managers focused on Veeva RIM (Regulatory Information Management), defining and executing the product strategy and roadmap to enhance regulatory process efficiency for life sciences customers.
- • Collaborate directly with engineering teams to translate product vision into technical specifications and deliver high-impact, scalable SaaS solutions that streamline regulatory submissions and compliance workflows.
- • Communicate product strategy, roadmap, and priorities clearly to internal stakeholders and external customers across global life sciences organizations, including pharmaceutical, biotech, and medical device companies.
- • Drive customer success by deeply understanding regulatory challenges faced by life sciences clients and aligning product development with evolving global regulatory requirements (e.g., FDA, EMA, PMDA).
- • Partner with cross-functional teams including sales, customer success, marketing, and support to ensure product-market fit and adoption of Veeva RIM solutions across key markets.
- • Own end-to-end product lifecycle management for Veeva RIM, from market research and requirement gathering to feature prioritization, release planning, and post-launch performance analysis.
- • Champion Veeva’s core values — Do the Right Thing, Customer Success, Employee Success, and Speed — in all product decisions and team interactions.
- • Foster a high-performance culture within the product team by mentoring Product Managers, encouraging innovation, and promoting data-informed decision-making.
- • Represent Veeva RIM internally and externally at industry events, customer meetings, and product forums to build thought leadership and gather market intelligence.
- • Leverage deep industry knowledge of life sciences regulatory processes to identify unmet needs and opportunities for product innovation that accelerate time-to-market for therapies.
- • Ensure product solutions comply with global regulatory standards and support customers in maintaining audit readiness and data integrity across regulatory submissions.
- • Work within Veeva’s Work Anywhere model, collaborating with distributed teams across North America, Europe, and Asia-Pacific to deliver a unified global product experience.
- • Contribute to Veeva’s mission as a Public Benefit Corporation by balancing customer, employee, societal, and investor interests in all product strategy decisions.
- • Stay current on emerging technologies and regulatory trends impacting life sciences compliance, and evaluate their applicability to Veeva RIM’s product roadmap.
- • Establish and track key product metrics to measure adoption, customer satisfaction, and business impact of Veeva RIM features and releases.
- • Act as the primary product advocate within the organization, aligning engineering, design, and operations teams around a shared vision for regulatory process transformation.
🎯 Requirements
- • Proven experience leading product management teams in SaaS or enterprise software environments
- • Deep understanding of life sciences regulatory processes (e.g., eCTD, CTMS, regulatory submissions)
- • Strong track record of defining and executing product strategy for complex B2B technology products
- • Experience working closely with engineering teams to deliver scalable cloud-based solutions
- • Excellent communication and stakeholder management skills across technical and non-technical audiences
- • Demonstrated ability to drive customer success and product adoption in regulated industries
🏖️ Benefits
- • Work Anywhere flexibility — choose to work from home or in the office
- • Opportunity to work at a Public Benefit Corporation legally bound to balancing stakeholder interests
- • Competitive compensation and equity package
- • Comprehensive health, wellness, and retirement benefits
Skills & Technologies
See exactly how your profile matches this role — strengths, skill gaps, and what to do about them.
About Veeva Systems Inc.
Veeva Systems provides cloud-based software for the global life-sciences industry. Its unified suite supports clinical, regulatory, quality, medical, and commercial functions, enabling pharmaceutical, biotechnology, and medical-device companies to manage data, documents, and workflows efficiently while meeting stringent compliance standards. Core products include Veeva Vault for content management, Veeva CRM for customer engagement, and Veeva R&D applications that accelerate drug development and regulatory submissions. Founded in 2007 and headquartered in Pleasanton, California, the company operates on a multi-tenant SaaS model, offering continuous updates and dedicated industry-specific data models, analytics, and collaboration tools trusted by more than 1,000 life-sciences organizations worldwide.
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