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Octapharma

Compulsory Internship in Regulatory Information Management, Submission Technology

Octapharma

. Support Computerized System Validation activities in accordance with GxP requirements .

Posted 10/14/2026internshipVienna • AustriaEntry Level💰 €2,051 per monthWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates strong analytical skills and attention to detail in supporting Computerized System Validation and data management activities. Proficient in preparing reports and dashboards using Power BI, with a foundational knowledge of SQL and software testing.

Highest-signal resume keywords
Computerized System ValidationData ManagementPower BISQLAnalytical Mindset

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Data VerificationData QualitySystem Test CasesValidation DocumentationSoftware TestingProgramming
Soft Skills
Problem-SolvingDetail-OrientedStructured Working StyleExcellent Communication Skills
Tools & Technologies
Microsoft OfficeExcel
Industry Keywords
GxP RequirementsRegulatory AffairsDigital SolutionsPharmaceutical IndustryBusiness Process Analysis

Tech Stack

Tools & technologies
SQL

About the role

Key responsibilities & impact
  • Support Computerized System Validation activities in accordance with GxP requirements
  • Prepare, execute and document system test cases and validation documentation
  • Support data migration, data verification and data quality activities
  • Maintain and analyze regulatory master data
  • Prepare reports and dashboards using tools such as Power BI
  • Assist in developing and maintaining Standard Operating Procedures, work instructions and system documentation
  • Support business process analysis and optimization initiatives
  • Provide administrative and project support to the Regulatory Information Management and Submission Technology team
  • Contribute to digital initiatives at the intersection of Regulatory Affairs, Information Technology and Data Management

Requirements

What you’ll need
  • Currently enrolled in a mandatory internship as part of a University of Applied Sciences (FH) degree program
  • Preferably studying Data Science or Business Analytics, Business Informatics, Software Engineering, Computer Science, Bioinformatics, Health Informatics, or Pharmaceutical or Biotechnology studies with a strong IT focus
  • Strong interest in digital solutions, data management and the pharmaceutical industry
  • Analytical mindset with excellent problem-solving skills
  • Structured and detail-oriented working style
  • Good knowledge of Microsoft Office, particularly Excel
  • Basic knowledge of SQL and Power BI
  • Software testing or programming is an advantage
  • Excellent English communication skills
  • German is an asset
  • Motivational Letter, CV, high school diploma, current transcript from university of Applied Science, and confirmation of mandatory internship required for application

Benefits

Comp & perks
  • A challenging and rewarding internship within an international pharmaceutical company
  • Hands-on experience with Regulatory Information Management, Computerized System Validation and digital transformation projects
  • Exposure to modern regulatory IT systems and data management processes
  • Mentorship from experienced professionals
  • An international and collaborative working environment
  • Company restaurant & meal subsidy
  • Training & further education
  • Health promotion
  • Parking spaces and good public transport connections
  • Company and team events