

Gazelle Global
Product Owner
β - Featured Role | Apply direct with Data Freelance Hub
This role is for a Product Owner with over 12 months' contract in London or Stevenage, requiring expertise in Planisware, GxP regulations, Agile methodologies, and experience in pharmaceutical or regulated environments. Pay rate is competitive.
π - Country
United Kingdom
π± - Currency
Β£ GBP
-
π° - Day rate
Unknown
-
ποΈ - Date
June 18, 2026
π - Duration
More than 6 months
-
ποΈ - Location
On-site
-
π - Contract
Fixed Term
-
π - Security
Unknown
-
π - Location detailed
London Area, United Kingdom
-
π§ - Skills detailed
#Compliance #Agile #Data Integrity #Consulting #Business Analysis #Scrum #Documentation #Kanban
Role description
Product Owner (Planisware)
As a supplier to one of our pharmaceutical organisations, I am seeking for a Product Owner for a 12 months+ contract in London or Stevenage.
Responsibilities:
We are looking for a seasoned Product Owner with strong experience in pharmaceutical or other highly regulated environments including Planisware skills. The candidate will be responsible for defining the product vision and roadmap for Planisware set of applications, ensuring alignment with business needs, scientific workflows, and compliance expectations. They must be able to work closely with cross functional teams to translate complex processes into clear product requirements and maintain a well-structured backlog. The role requires experience in Agile delivery, with accountability for ensuring that product increments meet GxP, data integrity, and validation standards. The individual should be comfortable collaborating with diverse stakeholdersβscientific, technical, and quality teamsβand communicating progress and risks effectively.
Experience:
β’ Proven experience as a Product Owner, Business Analyst, or similar role within pharmaceutical, life sciences, or other regulated industries.
β’ Strong understanding and expertise in Planisware skills to drive roadmaps.
β’ Strong understanding of GxP regulations, including 21 CFR Part 11, Annex 11, and data integrity principles (ALCOA+).
β’ Hands on experience supporting Computer System Validation (CSV) / Computer Software Assurance (CSA) processes, validation documentation, and audit readiness.
β’ Demonstrated ability to translate complex scientific, clinical, or manufacturing workflows into clear product requirements.
β’ Solid working knowledge of Agile methodologies (Scrum/Kanban) with experience leading Agile ceremonies.
β’ Experience collaborating with scientific, clinical, engineering, quality, or manufacturing teams in a cross functional setup.
Please apply with an updated CV, if interested or looking for a new opportunity as soon as possible.
Stefan Owusu-Francois
Recruitment Consultant
Gazelle Global Consulting
Tel: +44 20 3588 7771
stefan@gazellegc.com
Product Owner (Planisware)
As a supplier to one of our pharmaceutical organisations, I am seeking for a Product Owner for a 12 months+ contract in London or Stevenage.
Responsibilities:
We are looking for a seasoned Product Owner with strong experience in pharmaceutical or other highly regulated environments including Planisware skills. The candidate will be responsible for defining the product vision and roadmap for Planisware set of applications, ensuring alignment with business needs, scientific workflows, and compliance expectations. They must be able to work closely with cross functional teams to translate complex processes into clear product requirements and maintain a well-structured backlog. The role requires experience in Agile delivery, with accountability for ensuring that product increments meet GxP, data integrity, and validation standards. The individual should be comfortable collaborating with diverse stakeholdersβscientific, technical, and quality teamsβand communicating progress and risks effectively.
Experience:
β’ Proven experience as a Product Owner, Business Analyst, or similar role within pharmaceutical, life sciences, or other regulated industries.
β’ Strong understanding and expertise in Planisware skills to drive roadmaps.
β’ Strong understanding of GxP regulations, including 21 CFR Part 11, Annex 11, and data integrity principles (ALCOA+).
β’ Hands on experience supporting Computer System Validation (CSV) / Computer Software Assurance (CSA) processes, validation documentation, and audit readiness.
β’ Demonstrated ability to translate complex scientific, clinical, or manufacturing workflows into clear product requirements.
β’ Solid working knowledge of Agile methodologies (Scrum/Kanban) with experience leading Agile ceremonies.
β’ Experience collaborating with scientific, clinical, engineering, quality, or manufacturing teams in a cross functional setup.
Please apply with an updated CV, if interested or looking for a new opportunity as soon as possible.
Stefan Owusu-Francois
Recruitment Consultant
Gazelle Global Consulting
Tel: +44 20 3588 7771
stefan@gazellegc.com






