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Computer System Validation Intern
5 ore fa
We're Hiring: Computer System Validation (CSV) Intern at Arithmos
Are you a Life Sciences student or recent graduate interested in quality, compliance, and validated computerized systems?
Do you want hands-on experience in ensuring that critical systems used in pharma and life sciences meet regulatory standards?
Join
Arithmos
, a leading consultancy in IT and digital solutions for Life Sciences, and support global pharmaceutical and biotech companies in maintaining compliant and reliable GxP systems.
About Us
Arithmos is a leading international company operating in the Life Sciences and Technology fields. Headquartered in Italy with offices in the UK, we partner with pharmaceutical, biotech, and healthcare organizations across
Clinical, Regulatory, Quality, Pharmacovigilance, and Medical Affairs
.
We help our clients achieve operational excellence through technology-enabled solutions, ensuring quality, compliance, and innovation across the product lifecycle.
About the Role
As a
CSV Intern
, you will support our Computer System Validation team in ensuring that computerized systems are properly validated and maintained in a compliant state.
You will gain hands-on experience across the
GxP system lifecycle
, working alongside experienced CSV specialists on real client projects in a regulated environment.
Main Activities and Responsibilities
• Support the development of validation strategies and GxP system lifecycle documentation (plans, requirements, design documents, test protocols, release and maintenance documentation) in line with
GAMP 5
and internal SOPs
• Assist in ensuring compliance of computerized systems with applicable regulations (cGMP, GCP, GAMP, Data Integrity)
• Support the project team in applying CSV methodologies correctly
• Collaborate in GxP system risk assessments with internal teams and system stakeholders
• Assist in managing system change controls and related documentation
• Cooperate with technical teams during investigations of validation deviations or incidents
• Support the review of changes to validated systems to maintain validation status
• Assist Senior CSV Specialists during client audits and regulatory inspections
Knowledge and Qualifications
• Currently pursuing or recently completed a degree in
Life Sciences or Scientific disciplines
(e.g. Bioinformatics, Biomedical Engineering or similar)
• Strong interest in
Life Sciences, Pharma, and regulated environments
• Basic knowledge of CSV principles and computerized system compliance is a plus
• Awareness of data integrity and computer information regulations (e.g. privacy requirements)
• Fluent in
Italian
and
English
• Detail-oriented mindset with good analytical and organizational skills
Why Arithmos?
• Gain practical, hands-on experience in
Computer System Validation
• Work in a collaborative and international consulting environment
• Learn directly from experienced CSV professionals through mentorship and training
• Contribute to impactful projects that support compliance and quality in global healthcare
Place of work:
Verona/Milan, Italy
Apply now
and start your journey in Computer System Validation with Arithmos