Full-Time

Senior Software Engineer in Test

Veeva Systems

Veeva Systems

5,001-10,000 employees

Cloud-based quality, regulatory, and claims management

Compensation Overview

CA$90k - CA$150k/yr

+ Variable Bonus + Stock Bonus

Toronto, ON, Canada

Remote

Category
Software Engineering (1)
Required Skills
Software Testing
Git
Java
Gradle
Jenkins
Maven
REST APIs
Requirements
  • 7+ years of experience in software test automation or software development
  • Strong experience in Java, Object-Oriented Methodologies
  • Experience with API automation using REST Assured
  • Good understanding of modern best practices for software development like design patterns, code reusability, extensibility, and maintainability
  • Experience and ability in developing test automation frameworks from scratch or familiarity with one or more existing automation frameworks
  • Good working knowledge using tools such as Git, Jenkins, and Maven/Gradle
  • Problem-solving, Process Improvement, and Coaching
  • Strong written and verbal English skills to support complex analysis
  • Bachelor’s degree in Computer Science/Engineering or equivalent
Responsibilities
  • Define automation strategies
  • Design and develop new automation frameworks
  • Maintain and improve existing automation test suites
  • Monitor, analyze, and report test automation results
  • Contribute to automation infrastructure improvements
  • Collaborate with Developers, QA, and Product Managers to identify automation test cases that will ensure product quality
Desired Qualifications
  • Experience working in Unix/Linux and AWS environments
  • Experience with automation projects in JavaScript or Python

Veeva Systems provides cloud-based software that helps consumer goods and chemical companies manage quality, regulatory compliance, and advertising claims. The platform works by connecting different departments—from the supply chain to marketing—to provide a single source of data that tracks a product's journey and ensures it meets safety standards. Unlike competitors that offer general business tools, Veeva specializes in navigating the highly complex regulations originally found in the life sciences sector and applies that specific expertise to other regulated industries. The company's goal is to help businesses bring safe, sustainable, and compliant products to market faster by providing end-to-end visibility and traceability.

Company Size

5,001-10,000

Company Stage

IPO

Headquarters

Pleasanton, California

Founded

2007

Simplify Jobs

Simplify's Take

What believers are saying

  • Snowflake partnership on May 6, 2026, enables AI analytics on Vault data without migration.
  • 125 customers live on Vault CRM drives 16% YoY revenue growth to $3.2 billion.
  • S&P 500 inclusion on May 7, 2026, boosts stock liquidity despite 30% 2025 decline.

What critics are saying

  • Bares Capital cuts 21% stake in Q3 2025 amid slowing 16% revenue growth.
  • Legacy CRM support ends December 2029, forcing migration with adoption delays.
  • OpenAI partnerships with Pfizer and Merck supplant Vault AI in 18-36 months.

What makes Veeva Systems unique

  • Veeva Vault centralizes clinical, regulatory, and quality management on Salesforce platform.
  • Veeva CRM specializes in life sciences sales force compliance and HCP engagement.
  • Industry cloud unifies R&D, quality, and commercial workflows exclusively for pharma.

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Benefits

Parental leave

PTO

Free food

Health, dental, & vision insurance

Gym membership reimbursement

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

0%
Compliance in Pharma
Apr 10th, 2026
Validfor vs Veeva Vault QMS: which QMS platform is better in 2026?

Validfor vs Veeva Vault QMS: which QMS platform is better in 2026? Last updated: April 10, 2026 9:46 am Quality Management Systems (QMS) are essential for organizations in regulated industries such as pharmaceuticals, biotechnology, and medical devices. Choosing the right platform affects compliance, operational efficiency, and long-term scalability. In this comparison, Compliance in Pharma explore Validfor and Veeva Vault QMS to help you determine which solution best fits your needs. Overview of Validfor. Validfor is a modern validation-focused platform built with an automation-first approach. It focuses on continuous compliance, workflow automation, and reducing manual validation effort. Validfor is ideal for organizations seeking speed, flexibility, and efficiency. Overview of Veeva Vault QMS. Veeva Vault QMS is a cloud-based QMS platform designed specifically for life sciences. It provides comprehensive quality management capabilities, including document control, training, CAPA, and audit management. Veeva Vault QMS is widely used by global pharmaceutical and biotech companies. Key differences. 1. Platform focus. Validfor is primarily focused on validation automation and continuous compliance. Veeva Vault QMS is a full QMS platform covering all quality processes. 2. Automation. Validfor is built with automation at its core, enabling real-time validation and reduced manual effort. Veeva Vault QMS offers automation across quality processes but follows a more structured QMS framework. 3. Ease of use. Validfor provides a modern, user-friendly interface designed for fast adoption. Veeva Vault QMS has a robust interface but may require training due to its extensive features. 4. Implementation speed. Validfor is designed for rapid deployment and quick onboarding. Veeva Vault QMS implementations can take longer, especially in large enterprises. 5. Scalability. Both platforms are highly scalable. Validfor is well-suited for agile teams, while Veeva Vault QMS is optimized for large global organizations. 6. Compliance. Both platforms support GxP and regulatory compliance. Veeva Vault QMS has a strong track record in life sciences, while Validfor emphasizes continuous compliance through automation. Pros and cons. Validfor. * Automation-first approach * Fast implementation * Modern and intuitive interface * Continuous compliance capabilities * Limited full QMS functionality Veeva Vault QMS. * Comprehensive QMS features * Strong life sciences specialization * Global scalability * Longer implementation time * More complex setup and usage Which one should you choose? The best choice depends on your organization's scope and priorities. * Choose Validfor if: You want automation, speed, and validation-focused workflows * Choose Veeva Vault QMS if: You need a full QMS platform for enterprise-scale operations Final thoughts. Validfor and Veeva Vault QMS serve different roles within regulated environments. Veeva Vault QMS provides a comprehensive, enterprise-grade QMS solution, while Validfor represents a modern, automation-driven approach to validation. By aligning your choice with your operational needs, you can achieve better compliance, efficiency, and scalability. In recent years, validation processes across the pharmaceutical industry have been undergoing a major transformation. Workflows that were traditionally managed through paper documentation, spreadsheets and manual review cycles are increasingly moving toward digital validation platforms. As a result, life sciences organizations often evaluate solutions such as Kneat, Validfor, ValGenesis, MasterControl and Veeva when modernizing validation lifecycle management and compliance documentation. News & research. Audit management is a vital process in regulated industries such as pharmaceuticals, biotechnology, and medical devices. Organizations must plan, execute,... April 10, 2026 Validfor is rapidly emerging as a next-generation digital validation platform, designed to address the evolving needs of modern pharmaceutical and... April 10, 2026 Inspection readiness is about retrieval speed During an inspection, the biggest risk is not the absence of controls. It is... April 9, 2026 In highly regulated industries, validation and quality management systems play a critical role in ensuring compliance, product quality, and operational... April 9, 2026

Missouri Southern State University
Apr 8th, 2026
Missouri Southern to host Global Leaders Speaker Series, featuring Dr. Monicca Shanthanelson.

Missouri Southern to host Global Leaders Speaker Series, featuring Dr. Monicca Shanthanelson. Missouri Southern State University (MSSU) will host the Global Leaders Speaker Series on Monday, April 13, in the Ron Richard Athletic Center from 6 p.m. to 8 p.m. The event is free and open to the public. The series aims to inspire and inform attendees interested in scientific innovation and global leadership to build a more connected world. 0This event will feature a keynote address by Dr. Monicca Shanthanelson, a global Medical Affairs executive with more than 15 years of experience in enterprise medical strategy, scientific communications, and organizational leadership across oncology and neuroscience. She holds a PhD in Neuroscience from Stony Brook University and earned dual undergraduate degrees in Biology and Chemistry from Missouri Southern State University. "Giving our students the opportunity to hear from experts in a diverse set of fields lets them learn leadership and global citizenship skills from people who have lived experience in both of those areas," said Benjamin Cooper, MSSU's Director of Global Leaders. "Bringing Dr. Shanthanelson back to the MSSU campus is an exciting opportunity for them to learn from someone who was once in their position and has gone on to have global reach in her career." She currently serves as Scientific Director of Cross-Oncology Strategy within Global Medical Affairs at AbbVie, where she leads initiatives that align medical teams across international markets. In her many impressive roles, Dr. Shanthanelson has developed global frameworks to expand the reach of clinical data and improve coordination across major groups. Her work has contributed to measurable operational efficiencies and the adoption of standardized practices across global oncology teams, making a true impact. Prior to joining AbbVie, Dr. Shanthanelson served as Vice President and Global Head of Medical Affairs Business Consulting at Veeva Systems. There, she advised life sciences organizations and executive Medical Affairs leaders on global strategy, omnichannel engagement transformation, insight generation, and digital enablement of scientific exchange while owning profitability and client satisfaction. She also held senior leadership roles at MedThink SciCom (now FingerPaint Medical) where she supported pharmaceutical clients worldwide. With her impressive array of accomplishments, attendees of the Global Leaders Speaker Series are guaranteed to walk away with fresh insight from Dr. Shanthanelson. About Global Leaders Speaker Series Missouri Southern's Global Leaders Speaker Series reflects the university's ongoing commitment to fostering global perspectives and connecting students and the community with leaders and visionaries shaping the future of their industries. Through events like this, the university continues to create spaces and opportunities for meaningful dialogue, propagating students' learning and engagement beyond the classroom. For more information about the Global Leaders program, visit the program webpage.

Yahoo Finance
Mar 14th, 2026
Veeva Systems posts 13.6% CAGR since 2013 IPO amid growing cloud competition

Veeva Systems, a cloud solutions provider for the life sciences industry, has delivered a 13.6% compound annual growth rate since its 2013 IPO. The company serves 15 of the top 20 biopharma companies and benefits from high switching costs, as clients depend on its platform for critical functions like clinical trial data management and regulatory compliance. Despite revenue growth slowing as the company matures, Veeva estimates its total addressable market at $20 billion against trailing-12-month revenue of $3.2 billion. The company is also expanding into new sectors including cosmetics, consumer packaged goods and chemicals. To turn a $70,000 investment into $2 million over 30 years would require an 11.82% CAGR, slightly below Veeva's historical performance but achievable given its market position and growth opportunities.

Yahoo Finance
Mar 13th, 2026
Veeva Systems fair value estimate cut to $270.93 as analysts trim targets amid software sector pressure

Veeva Systems' fair value estimate has been cut from $302.60 to $270.93, a roughly 10% reduction reflecting more cautious assumptions. The adjustment comes amid mixed analyst sentiment, with firms trimming price targets despite pointing to strong Q4 execution and solid profitability. Several analysts, including Citi, TD Cowen and Piper Sandler, highlighted Veeva's strong Q4 performance, with billings and guidance exceeding consensus and operating margins reaching 43.8%. Some firms view Veeva as well-positioned against AI-related risks due to its integrated platform. However, Goldman Sachs maintains a Sell rating with a $190 target, citing concerns around CRM competition and AI positioning. Multiple firms have lowered targets due to software sector compression and scepticism around growth sustainability. Morgan Stanley upgraded to Equal Weight in February.

pharmaphorum
Mar 11th, 2026
Veeva buys brand engagement firm Ostro for $100m

Veeva buys brand engagement firm Ostro for $100m. Veeva Systems Veeva CEO Peter Gassner. Veeva Systems has built its presence in brand engagement with the acquisition of Ostro, a tech start-up that helps pharma companies connect with doctors and patients using AI-powered conversational tools. The deal - valued at around $100 million in cash and long-term equity retention grants - will allow Ostro's engagement system to be integrated with Veeva's Commercial Cloud, a suite of software, data, and analytics used by life sciences companies to manage sales, marketing, and medical functions. Miami, Florida-based Ostro - which was founded in 2019 - will operate as an independent unit of Veeva and will continue to be led by co-founder and chief executive Chase Feiger, according to a statement issued by the two companies. "We're focused on shortening the time it takes to identify and treat health conditions," said Feiger. "We built Ostro to remove friction so patients and doctors can get trusted answers with less clicking, thinking, and scrolling. With Veeva, we can bring that experience to many more patients, doctors, and brands." Ostro's conversational AI and semantic search tools allow customers to easily ask questions and receive approved information, resources, and next steps in real-time, according to the statement. The company's tools are used by around half of the top 20 pharma companies, helping to deliver tailored content to healthcare professionals and guide patients to appropriate treatments. The platform can also be used to come up with pointers to help brands improve their reach and engagement. Ostro says responses from its platform, drawn exclusively from pre-approved medical, legal, and regulatory materials, are 100% compliant with regulations. "AI has changed how people get information. It's no longer about how much information you can put out there, it's about how easy it is for customers to get answers," said Veeva CEO Peter Gassner. "Ostro is leading the way in helping brands ensure patients and doctors have instant access to accurate information," he added. This is the second company acquired by Veeva this year, with the deal announced shortly after it bought Yonalink to bolster its position in clinical trial management, taking control of its AI-enabled electronic data capture (EDC) platform for harvesting electronic health record data, which is used to reduce manual data entry and errors and speed up trials. The acquisitions should build on a strong growth trajectory at Veeva, which earlier this month reported revenues up 16% to $3.2 billion, with 767 customers for Commercial Solutions and 1,196 for its R&D and Quality Solutions suite. 11 March, 2026