CSV Analyst Global Apps (m/f/d)
Halian
As an IT CSV Expert Analyst – Global Applications, you will be responsible for ensuring compliance and validation of non-GMP applications, including clinical and reporting applications, within IT Compliance Solutions team. You will work closely with IT system owners, business stakeholders, and compliance leads to manage validation activities, documentation, and audits.Key Responsibilities
? Validation Requirement Assessment
? Validation Plan & Report
? Test Protocols (IQ/OQ/PQ/MQ) & Reports
? Traceability Matrix
Required Qualifications & Skills? Minimum 3 years of experience in Computer System Validation (CSV) within a regulated environment.
? Strong expertise in validation of pharma applications, including:
? GPVP (e.g., Adverse Event Reporting: Argus, ArisG, Veeva Safety)
? GCP (e.g., Clinical Trial Monitoring: CTMS)
? General Pharma Systems (QMS, Learning, Testing, Medical Applications)
? Experience with compliance/validation of mobile & web applications.
? Familiarity with Veeva systems is a plus.
? Knowledge of cloud platforms (Azure, AWS), monitoring tools, identity & access management, and communication platforms (Office 365, Skype, Exchange) is beneficial.
? Strong stakeholder management, communication, and negotiation skills.
? Ability to work autonomously with a proactive and problem-solving mindset.
? High attention to detail and ability to handle compliance documentation effectively.
? Fluent in English (mandatory); French is a plus.#LI-SD2
Bruxelles
Tue, 25 Feb 2025 23:45:06 GMT
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