Senior Manager, Product Management – MSAT

ValGenesis, Inc.; Chennai District; On-site; INR 2,500,000 - 3,500,000; Full time

Job summary

ValGenesis, Inc. is seeking a Senior Manager of Product Management to shape MSAT software for life sciences. You’ll own eBR, technology transfer, and APQR product areas, turning regulatory workflows into scalable software with AI-driven prototyping.

You’ll collaborate with leadership, Engineering, SMEs, and GTM teams to drive from roadmap to launch and adoption. You’ll apply deep domain knowledge of pharmaceutical manufacturing and validation, ensuring regulatory alignment and high-quality

Qualifications

• Bachelor's degree in Life Sciences, Engineering, Computer Science or related field; advanced degree a plus.
• 8+ years in MSAT, pharmaceutical manufacturing, validation, quality systems, or regulated life sciences software.
• 3+ years in Product Management or related software delivery role, ideally enterprise SaaS.
• Hands-on MSAT workflows such as tech transfer, batch execution/eBR, validation, and ATP.
• Strong regulatory/computerized systems knowledge (FDA 21 CFR Part 11, EU Annex 11, etc.).
• Experience translating complex requirements into user stories and acceptance criteria.
• Experience backlog prioritization in Agile/Scrum; proficiency with AI-enabled discovery.
• Excellent written and verbal communication across technical and commercial audiences.

Responsibilities

• Translate roadmap into epics, user stories, and specs for eBR, Tech Transfer and APQR.
• Own and prioritise the product backlog; balance competing requirements for value.
• Lead requirements walkthroughs with Engineering; translate complex concepts clearly.
• Create AI-enabled prototypes, workflows and mockups to visualize concepts.
• Coordinate releases with Sales, Marketing, Success for clear messaging.
• Use data and feedback to guide product decisions and optimize adoption.

Skills

MSAT knowledge

Product management

Agile/Scrum

AI capabilities

Requirements gathering

Stakeholder collaboration

Communication

Regulatory knowledge

Education

Bachelor's degree

Tools

ValGenesis

Kneat

MasterControl

TrackWise

Veeva

Job description

ValGenesis is transforming how life sciences companies manage some of their most complex and highly regulated manufacturing processes — and we’re looking for a Senior Manager, Product Management to help shape what comes next.

In this role, you’ll own the execution and evolution of key MSAT product areas, including Electronic Batch Records (eBR), Technology Transfer, and Annual Product Quality Review (APQR). You’ll bring together deep life sciences domain knowledge, product thinking, and emerging AI capabilities to turn complex manufacturing and regulatory workflows into intuitive, scalable software.

This is a hands‑on product role for someone who understands both sides of the equation: how MSAT teams operate in the real world and how great software gets built. You’ll work closely with Product leadership, Engineering, subject matter experts, and go‑to‑market teams to take ideas from roadmap through requirements, prototyping, delivery, launch, and adoption.

You’ll also have the opportunity to rethink traditional product development approaches by using AI to rapidly prototype concepts, accelerate requirements development, and communicate product intent more effectively.

What You’ll Own

• Drive MSAT product execution. Translate product strategy and roadmap priorities into clear product requirements, epics, user stories, and specifications across eBR, Tech Transfer, and APQR.
• Bring deep domain expertise into the product. Apply your understanding of pharmaceutical manufacturing, MSAT processes, validation, data integrity, and regulatory expectations to ensure we build solutions that solve real customer problems.
• Own and prioritize the product backlog. Make day‑to‑day prioritization decisions, balance competing requirements, and keep delivery focused on the highest‑value outcomes.
• Turn ideas into something tangible. Use AI‑enabled tools to rapidly create prototypes, workflows, and mockups that help teams visualize concepts, challenge assumptions, and move from idea to execution faster.
• Be the bridge between domain and technology. Lead requirements walkthroughs and working sessions with Engineering, translating complex manufacturing, quality, and regulatory concepts into requirements technical teams can confidently build against.
• Raise the quality of AI‑assisted product development. Review and refine AI‑generated acceptance criteria, functional specifications, prototypes, and other product artifacts to ensure they are accurate, complete, usable, and appropriate for a regulated environment.
• Drive products through delivery. Partner with Engineering, Product Owners, Business Analysts, and SMEs throughout backlog refinement, sprint planning, reviews, testing, and release planning while surfacing risks and dependencies early.
• Support successful product launches. Partner with Sales, Product Marketing, Customer Success, and other teams to translate new capabilities into clear release communications, enablement materials, and customer‑facing messaging.
• Use data to improve the product. Monitor adoption, usage, customer feedback, enhancement requests, and defect trends to identify opportunities and inform future product decisions.

What You Bring

• Bachelor’s degree in Life Sciences, Engineering, Computer Science, or a related field; an advanced degree is a plus.
• 8+ years of experience spanning MSAT, pharmaceutical manufacturing, computer system validation, quality systems, and/or regulated life sciences software within pharmaceutical, biotechnology, or medical device environments.
• 3+ years of experience in Product Management, Product Ownership, Business Analysis, or a comparable software product delivery role, ideally within enterprise SaaS.
• Hands‑on understanding of MSAT workflows such as technology transfer, batch execution/eBR, process validation, continued process verification, and/or annual product quality review.
• Strong understanding of regulated computerized systems and applicable frameworks, including FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ICH Q7/Q9/Q10, ASTM E3106/E3263, and ALCOA+ data integrity principles.
• Demonstrated experience translating complex business or regulatory requirements into user stories, workflows, acceptance criteria, and functional requirements that Engineering teams can execute.
• Experience managing and prioritizing a product backlog within an Agile/Scrum software development environment.
• Practical experience using generative AI tools such as ChatGPT, Claude, or similar platforms to accelerate product discovery, requirements development, prototyping, or problem‑solving.
• Strong written and verbal communication skills, with the ability to work effectively across highly technical, scientific, and commercial audiences.

Even Better If You Have

• Experience with MES, eBR, validation lifecycle management (VLMS), LIMS, eQMS, technology transfer, or other pharmaceutical manufacturing software.
• Experience with platforms such as ValGenesis, Kneat, MasterControl, TrackWise, Veeva, or comparable regulated enterprise applications.
• Previous experience working for a SaaS or enterprise software company serving pharmaceutical or biotechnology customers.
• Experience introducing AI‑enabled capabilities or workflows into regulated enterprise software.
• Quality, validation, Agile, or product management certifications such as ASQ CQE/CQA, CSPO, or Pragmatic Institute.

We’re on a Mission

In 2005, we disrupted the life sciences industry by introducing the world’s first digital validation lifecycle management system. ValGenesis VLMS® revolutionized compliance‑based corporate validation activities and has remained the industry standard.

Today, we continue to push the boundaries of innovation ― enhancing and expanding our portfolio beyond validation with an end‑to‑end digital transformation platform. We combine our purpose‑built systems with world‑class consulting services to help every facet of GxP meet evolving regulations and quality expectations.

The Team You’ll Join

Our customers’ success is our success. We keep the customer experience centered in our decisions, from product to marketing to sales to services to support. Life sciences companies exist to improve humanity’s quality of life, and we honor that mission.

We work together. We communicate openly, support each other without reservation, and never hesitate to wear multiple hats to get the job done.

We think big. Innovation is the heart of ValGenesis. That spirit drives product development as well as personal growth. We never stop aiming upward.

We’re in it to win it. We’re on a path to becoming the number one intelligent validation platform in the market, and we won’t settle for anything less than being a market leader.

How We Work

Our Chennai, Hyderabad and Bangalore offices are onsite, 5 days per week. We believe that in‑person interaction and collaboration fosters creativity, and a sense of community, and is critical to our future success as a company.

ValGenesis is an equal‑opportunity employer that makes employment decisions on the basis of merit. Our goal is to have the best‑qualified people in every job. All qualified applicants will receive consideration for employment without regard to race, religion, sex, sexual orientation, gender identity, national origin, disability, or any other characteristics protected by local law.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.