[H04] - Product Owner – Pharmacovigilance (PV) Applications

[H04] - Product Owner – Pharmacovigilance (PV) Applications

23 Mar
Bangalore Rural

23 Mar


Bangalore Rural

Product Owner - Pharmacovigilance (PV) Applications

Job Code

: DQ121-07

Posted on

: March 23, 2021

Job Location

: Bangalore/Noida


: Healthcare/Lifesciences


: Product Management


The Product Owner (PO) is directly accountable for the definition and delivery of a part of a platform/suite or module from a customer and regulatory market requirement point of view – regarding content, prioritization, quality, and customer excitement for a given cost and time frame. The PO shall be responsible for a part of the platform/suite or module through the product life cycle from the definition to the phase-out.

The PO shall provide to the associated development teams with the priorities and expertise regarding the product and responsible for definition and delivery of a part of a product from a customer and market requirement point of view, working with one or several development teams.

Internal Interactions: Product Line Manager, Product Manager, Project Manager, Quality Manager, Development Team (e.g. Scrum Master, System Analyst, Architect, Developers, Testers), other stakeholders (e.g. Business Units), SCM (Enabling) & Customer Service teams, Technical Writers, etc.

External Interactions: Customers – PV Head, PV Operations Managers, Subject Matter Experts, Business Users etc.


- Elicit and collect stakeholder requests, while you define and prioritize Regulatory Requirements

- Analyse Regulatory Requirements (e.g. initiate and manage concepts for complex regulatory and market requirements)

- Derive, prioritize and communicate Software Requirements

- Create Software Requirement Specifications (i.e. problem part)

- Ensures user stories are captured in detail for development to start work.

- Coach/ support development team’s questions and resolve conflict regarding features and requirements

- Analyse and decide complaints and charms

- Achieve commitments with and motivate development teams, assist development teams in attaining maximum effective sustainable pace for development

- Define product vision, roadmap, and growth opportunities and provide backlog management, iteration planning, and elaboration of the user stories.

- Ensure quality by evaluating results of iterations and either approve/ accept or reject results based on acceptance criteria

- Plan and prioritize product backlog and development for the product. Lead the planning product release plans and set the expectation for delivery of new functionalities.

- Support effort estimations of development teams

- Analyse change request entries and prioritize with other product backlog items

- Coordinate cross-feature-area development with peers to facilitate prioritized product development

- Deliver input for project management, support roll-out of the system, presentation, workshops, training for sales and customer demos.

- Hands on technical documentations such as Requirement Specification Document, Business Requirement Document, SOW and so on.

- Provide an active role in mitigating impediments impacting successful team completion of Release/Sprint Goals.

- Keep updated with Agile/Scrum best practices and new trends.

- Ability to participate in client demos, probe questions, work towards building pipeline for future release.

- Research and analyse the market, the customers, and the roadmap for the product.


- A Bachelors’ / master’s degree in life sciences, engineering and / or MCA or equivalent.

- 10-12 years of experience as a Business Analyst or Product Manager or Product Owner for a minimum of 3 years.

- Desired knowledge & experience in healthcare market, drug development lifecycle, end-to-end pharmacovigilance lifecycle and regulatory affairs, medical review of safety reports.

- Product know-how and customer understanding: sound knowledge of Clinical and Healthcare IT, especially in adverse event management, healthcare industry standards like HL7, DICOM and IHE.

- Good understanding of software systems categorized as medical device, drug and vaccine with intermediate knowledge of veterinary-vigilance, cosmetic vigilance and evolving vigilance sciences.

- Basic understanding of Legal regulations and standards applicable for drugs, vaccines and medical devices, affecting all aspects of safety (i.e. FDA 21CFR820QSR, ISO 13485)

- Exposure to agile methodology, thorough experience in requirements engineering, usability engineering and feature definition activities.

- Product Lifecycle Management & Software development cycle experience.

- Possessing success skills – Self driven and takes Initiatives, Decision making skills, Result orientation, Self-motivated and provides motivation and inspiration to the team, Strong Analytical and Problem-Solving Skills. Strong team player and networking skills. Strong written and oral communication skills. Strong interpersonal skills and mainly, a strong customer focus.

To apply for the above position, please send your word resumes to [email protected] by specifying the Job Code.

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