Computerized Systems & Data Integrity Junior Specialist

About the Role
This is not a typical IT role, nor is it solely a QA documentation role. We are looking for a person who wants to grow in the area where pharmaceutical manufacturing, computerized systems, GMP compliance, data integrity, and digital transformation meet. The role is suitable for both candidates with initial experience in CSV, GMP, IT systems, QA, QC, or production systems, as well as motivated graduates who are willing to learn. You will work with computerized systems used in GMP processes and support their validation, maintenance, administration, and continuous improvement. This role is a good opportunity for someone who wants to build a long-term career in pharma digitalization, CSV, data integrity, or GxP IT.
This role may be suitable for you if:
• You are interested in digital tools, data, or automation
• You like understanding how systems work, not only using them
• You are careful with details and understand that data must be reliable
• You are willing to learn GMP, Annex 11, computerized system validation, and ALCOA+ principles
• You enjoy working with different departments such as IT, QA, QC, Production, Engineering, and Warehouse
• You are not afraid of documentation, but you also want to work with real systems and real business processes
Key Responsibilities:
• Support computerized system validation activities, including URS, Risk Assessment, IQ/OQ/PQ and validation reports
• Assist in maintaining GMP computerized systems in a validated state
• Participate in system administration, user access review, periodic review, backup/recovery checks, and change control activities
• Ensure compliance with data integrity and ALCOA+ principles
• Work with IT, QA, QC, Production, Engineering, and other departments to support system compliance