Product Owner

Product Owner
12 Month contract initially + Extensions
Based: London/Stevenage (Flexible) - Hybrid. Max 2-3 days p/w onsite
Rate: £Market rates p/d - (via Umbrella company)

We have a great opportunity with a world leading organisation where you will be provided with all of the support and development to succeed. A progressive organisation where you can really make a difference. We have a great opportunity for a number of Product Owner's to join the team.

Key Responsibilities
* Define and communicate the product vision and roadmap aligned with pharma business goals and regulatory timelines for Planisware set of applications.
* Ensure all product capabilities meet relevant compliance standards, including GxP, ALCOA+, 21 CFR Part 11, and Annex 11.
* Own and prioritize the product backlog, balancing business value, scientific needs, regulatory requirements, and technical debt.
* Translate complex scientific, clinical, or manufacturing workflows into actionable user stories with clear acceptance criteria.
* Collaborate closely with engineering, data, QA, design, and business SMEs to deliver validated and compliant product increments.
* Lead Agile ceremonies such as sprint planning, refinement sessions, and sprint reviews.
* Ensure all deliverables meet validated-state requirements for deployment in regulated environments.
* Engage with stakeholders across scientific, clinical, manufacturing, regulatory, and quality teams to gather requirements and share product updates.
* Monitor product KPIs, user adoption, operational efficiency, and compliance metrics to guide continuous improvement.
* Uphold strong data governance and data integrity principles while driving user centric, compliant product enhancements.

Key Skills & Experience:
* Proven experience as a Product Owner, Business Analyst, or similar role within pharmaceutical, life sciences, or other regulated industries.
* Strong understanding and expertise in Planisware skills to drive roadmaps.
* Strong understanding of GxP regulations, including 21 CFR Part 11, Annex 11, and data integrity principles (ALCOA+).
* Hands on experience supporting Computer System Validation (CSV)/Computer Software Assurance (CSA) processes, validation documentation, and audit readiness.
* Demonstrated ability to translate complex scientific, clinical, or manufacturing workflows into clear product requirements.
* Solid working knowledge of Agile methodologies (Scrum/Kanban) with experience leading Agile ceremonies.
* Experience collaborating with scientific, clinical, engineering, quality, or manufacturing teams in a cross functional setup.
* Ability to manage and prioritize a product backlog that balances business value, compliance needs, and technical constraints.
* Strong analytical and problem solving mindset, especially in regulated or high complexity environments.
* Excellent communication skills for engaging both technical and non technical stakeholders.
* Proven ability to operate in ambiguity, drive clarity, and make decisions in compliance driven environments.

This is an excellent opportunity on a great project of work, If you are looking for your next exciting opportunity, apply now for your CV to reach me directly, we will respond as soon as possible.

LA International is an award-winning partner of choice for many of the world's most influential companies and government organisations. Holding Enhanced Government Security Accreditation, we are recognised as the European market leader in the delivery of Security Cleared talent to organisations that demand the very highest levels of security, compliance and assurance.

A multiple award-winning organisation, having secured the prestigious Queens Award for Enterprise: International Trade over consecutive years. We are committed to fostering an inclusive, equitable and accessible workplace where everyone feels valued and supported. We welcome applications from all individuals, regardless of background or identity, and we encourage candidates who may not meet every listed requirement to still apply. If you require any adjustments or support during the recruitment process, please let us know and we will work with you to ensure a fair and accessible experience.

Please Note: If a high volume of applications is received, only candidates shortlisted will be contacted.