Davipharm

Job description

• Assist in the development and execution of computer system validation protocols and reports.
• Perform testing and documentation of computerized systems according to GMP guidelines.
• Support the development and maintenance of validation plans, procedures, and policies.
• Collaborate with cross-functional teams to ensure computerized systems compliance with regulatory requirements.
• Participate in the assessment and remediation of non-conformances related to computerized systems.
• Maintain up-to-date knowledge of industry regulations and best practices related to computerized system validation.

Job requirement

• Bachelor’s degree in Computer Science, Information technology, Pharmacy or related field.
• Experience in a GMP-regulated environment, preferably in the pharmaceutical industry.
• Basic Knowledge of FDA 21 CFR Part 11 and GMP Annex 11 regulations.
• Excellent communication, organization, and analytical skills.
• Ability to work independently and as part of a team.
• Good English skills

Please contact our Recruiter or apply via email recruitment@davipharm.info