Are you a seasoned CSV (Computer System Validation) professional looking for an exciting opportunity to lead transformative projects in the Life Sciences sector? We are partnering with a leading global Life Sciences organisation in search of a talented CSV expert to spearhead a pivotal CSV transformation program.
This is a remote role with travel once a month, and is available in Spain or the United Kingdom
Key Responsibilities:
Create and deliver CSV documentation, including Validation Plans, Requirements Specifications, Test Protocols, and Summary Reports.
Ensure security and compliance solutions meet QA and CSV procedures and regulatory standards.
Collaborate with project teams to gather information and ensure accurate documentation.
Review and update CSV documents for system and process changes.
Execute validation tests as needed.
Train and support project teams on CSV documentation requirements.
Stay updated with CSV best practices and regulatory requirements.
Ensure Agile projects comply with CSV requirements.
Coach colleagues on validation and qualification activities and support training on CSV compliance.
Qualifications:
Bachelor's degree in computer science, IT, or related field.
3+ years of experience in CSV compliance testing and documentation.
Knowledge of Waterfall and Agile project management methodologies.
Experience in CSV compliance for Agile projects.
Knowledge of GMP regulations and guidelines in pharmaceuticals.
Strong documentation skills with attention to detail and accuracy.
Ability to manage multiple tasks independently.
Effective communicator and team collaborator.
This is a rare opportunity to make a significant impact in a remote role with a globally recognised Life Sciences organisation. If you are ready to take the next step in your CSV career and drive meaningful change, we invite you to apply now!
Don't miss out on this exciting opportunity-apply today by submitting your CV!
CSV Consultant in Barcelona, Spain , Full-Time
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