Job Description:

• 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

Job Requirement:

• 0–2 years of experience in CSV, IT systems, QA, QC, Production, Engineering, or GMP environment
• Fresh graduates are welcome if you are motivated and eager to learn
• Experience or interest in Power BI, automation, AI, or data analysis
• Understanding of GMP, EU GMP Annex 11, CSV, or data integrity principles
• Basic knowledge of SQL (nice to have)
• Interest in digital transformation in pharmaceutical manufacturing
• English efficiency (daily work & communication within the team in English)
• Good attention to detail
• Logical thinking and willingness to investigate problems

Please contact our Recruiter or apply via email recruitment@adamed.com