Product Manager

5 days ago

Noida, India Opkey Full time
At Opkey, we empower enterprises to unlock the full potential of their ERP investments with cutting-edge, agentic AI-powered automation. Our intelligent platform delivers continuous assurance across the entire ERP lifecycle—from initial deployment to day-to-day operations and long-term digital transformation. By eliminating manual errors, accelerating testing cycles, and ensuring seamless adoption of critical updates, Opkey helps organizations modernize with confidence and agility. Trusted by 250+ global enterprises, we reduce risk, drive efficiency, cut costs, and fast-track innovation so businesses can focus on what they do best: growing and evolving in a dynamic digital world.
Opkey is seeking a Product Manager – Veeva Domain with 6+ years of experience who can shape the future of our automation products for the life sciences ecosystem. This role is ideal for someone who deeply understands Veeva applications (Vault, CRM, Quality, Regulatory, Safety, Promo Mats, Med Comms, etc.) You’ll drive automation capabilities that help global life sciences enterprises accelerate Veeva implementations, upgrades, compliance cycles, and validation—while collaborating with some of the sharpest minds across Engineering, Design, Sales, and Customer Success.
This is a high-visibility, high-impact role where you’ll be directly responsible for building Opkey’s Veeva-focused product line spanning testing, configuration, training, and compliance automation.

Develop automation for key Veeva products (Vault Quality Docs, QMS, RIM, Safety, CRM, Promo Mats) to reduce manual validation, accelerate configuration, and ensure compliance.

Compliance & Validation FocusEnsure that automation features address regulatory requirements such as GxP, 21 CFR Part 11, and Annex 11, enabling faster customer validation.

Data-Driven Improvements
Monitor product usage, adoption, and customer satisfaction metrics to continuously optimize product performance.

Your day might start by reviewing customer validation timelines and compliance-related challenges in ongoing Veeva projects. You’ll meet with engineering to discuss automation features for Vault QMS, align with design on usability, and check in with customer success on adoption trends. In the afternoon, you might run a product demo for a pharma client or refine a PRD for automating Promo Mats content validation. 6+ years of Product Management experience in SaaS/Enterprise Software, with at least 3+ years in life sciences / Veeva ecosystem.
Strong academic background (Bachelor’s/Master’s from a Tier-1 institute).
Hands-on knowledge of Veeva applications (Vault QMS, RIM, Safety, Promo Mats, CRM, Med Comms).
Familiarity with regulatory compliance frameworks (GxP, Part 11, Annex 11) and their impact on product validation.
Experience working in Agile/Scrum using tools like JIRA, Confluence, Aha, Exposure to automation for Veeva validation, testing, training, and configuration.
Clinical, Regulatory, Quality, Safety, and Commercial.
Prior experience with SaaS platforms, automation products, or working with Veeva partners (TCS, Cognizant, Accenture, etc.).

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