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Drug safety systems specialist

Recife
beBeeProduct
Anunciada dia 3 outubro
Descrição

As a key liaison between business stakeholders, regulatory teams, and IT professionals, the successful candidate will play a pivotal role in ensuring pharmacovigilance systems and workflows operate accurately, compliantly, and efficiently.They will be responsible for overseeing the product roadmap, aligning it with business priorities and driving strategic growth.Maintenance, rebuilding, and tech stack upgrades will also fall under their purview, including migrations such as CloudX to KCloud.Effective collaboration across Business, Infrastructure, and Leadership teams is crucial for planning and managing product releases, downtime, incidents, and upgrades.The individual will oversee system integrations (Argus, ArisG, Veeva Vault Safety) to ensure accurate data flow and reporting.Requirements:A Bachelor's degree in Life Sciences, Pharmacy, Information Technology, or a related field is essential.Strong experience as a Product Analyst or Business Analyst in a regulated environment is required.Proficiency in AWS for RCA/debugging and familiarity with Cloud/SaaS platforms are necessary.

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