INTERNSHIP DETAILS

Data Integrity / CSV Intern (Fixed term contract for 12 months)

CompanyJohnson & Johnson Innovative Medicine
LocationSchaffhausen
Work ModeOn Site
PostedFebruary 6, 2026
Internship Information
Core Responsibilities
The Data Integrity / CSV Intern will assist in the qualification of laboratory equipment to ensure compliance with cGMP standards and support the development and execution of qualification protocols. The intern will collaborate with laboratory personnel to troubleshoot equipment-related issues and maintain data integrity within laboratory systems.
Internship Type
full time
Company Size
37919
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
At Johnson & Johnson Innovative Medicine, we innovate with purpose, to lead where medicine is going. The experiences of patients around the world inform and inspire our science-based innovations, which continue to change and save lives. Applying rigorous science with compassion, we confidently address the most complex diseases of our time and develop the potential medicines of tomorrow. We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way. https://bit.ly/3reuMvK
About the Role

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:

Career Programs

Job Sub Function:

Non-LDP Intern/Co-Op

Job Category:

Career Program

All Job Posting Locations:

Schaffhausen, Switzerland

Job Description:

The role of Data Integrity / CSV Intern is supporting qualification projects focusing on computer system validation (CSV) and data integrity (DI) for laboratory equipment.

Key Responsibilities:

  • Assist in the qualification of laboratory equipment to ensure compliance with cGMP standards

  • Support the development and execution of qualification protocols (e.g., IOPQ)

  • Collaborate with laboratory personnel to troubleshoot and resolve equipment-related issues

  • Participate in routine maintenance of laboratory equipment (e.g., User Account Reviews, Backup & Recovery Testing)

  • Support efforts to maintain data integrity within laboratory systems and procedures

  • Assist in the review and validation of data management practices to ensure compliance with data integrity standards

  • Perform related duties as assigned by supervisor

  • Maintain compliance with all company policies and procedures

Minimum Qualification:

  • MSc/ BSc; Apprenticeship in Natural Sciences, Engineering, or alternatively a comparable education

  • Fluent in English

  • Excellent computer proficiency e.g. MS Office

  • Excellent analytical skill to identify gaps and root causes of issues and think out of the box to develop a solution

Preferred:

  • Experience working with pharmacopeia

  • Experience with various analytical techniques, preferably in a regulated environment

  • Hands on experience with instrument qualification and documentation (e.g., qualification of production plants, laboratory equipment)

  • Excellent analytical skills and problem-solving attitude

  • Experience with QMS, SAP is an advantage

 

 

Required Skills:

Analytical Thinking, Communication, Microsoft Excel

 

 

Preferred Skills:

Key Skills
Data IntegrityComputer System ValidationLaboratory EquipmentcGMP StandardsQualification ProtocolsTroubleshootingAnalytical TechniquesProblem-SolvingQMSSAPUser Account ReviewsBackup & Recovery TestingData Management PracticesComplianceAnalytical SkillsRoot Cause Analysis
Categories
HealthcareScience & ResearchEngineeringData & Analytics