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Planet Pharma in the Slough area is seeking a Safety Systems & Innovation Specialist to bridge pharmacovigilance operations, IT, and external suppliers. You will support and enhance safety systems, including Veeva Vault Safety, and lead upgrades and validation activities.
This hybrid role (2-3 days onsite) offers exposure to AI opportunities in patient safety, change controls, CAPAs, and data integrity practices within a global, collaborative environment.
Slough Area (Hybrid, 2-3 days onsite) Long-Term Contract Full-Time | 37.5 Hours Per Week
? Are you an experienced Pharmacovigilance Systems professional who enjoys bridging the gap between business operations, technology, and patient safety?
We're partnering with a leading global biopharmaceutical organisation to find a Safety Systems & Innovation Specialist who will play a key role supporting and enhancing the technology landscape that underpins patient safety and pharmacovigilance activities.
This is a highly visible, business-facing role where you'll work closely with Safety Operations, IT teams, external suppliers, and system experts to drive system improvements, support global upgrades, and identify innovative technology opportunities across the safety systems ecosystem.
5+ years' experience supporting Pharmacovigilance / Drug Safety systems
Strong knowledge of pharmacovigilance processes and operations
Experience working within GxP-regulated environments
Experience supporting validated computer systems
Excellent business analysis skills with the ability to translate operational requirements into system solutions
Strong stakeholder management and communication skills
Experience supporting system implementations, upgrades, releases and change management activities
Please note: This is not a software development or programming role. We're seeking someone with strong Pharmacovigilance Systems, Business Analysis, Validation and Safety Operations experience who can bridge business needs and technology solutions.
If you have experience supporting safety systems in a regulated environment and enjoy driving technology-enabled improvements across pharmacovigilance operations, we'd love to hear from you.