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Job Description: Elaborate and review protocols related to software validation of equipment and systems, perform proposed tests, and prepare relevant reports.
Develop and review risk matrices associated with software validations.
Review documentation from third-party companies related to software validations of production, laboratory, and utility equipment linked to your responsibilities, including monitoring.
Create and review operational procedures related to your responsibilities.
Investigate failures and deviations during validation processes and participate in Non-Conformance Reports (RNC) meetings.
Engage in risk analysis meetings related to your activities.
Manage Change Control processes associated with your tasks.
Evaluate and execute IT service orders related to software validations.
Update activity control spreadsheets and schedules.
Perform other similar tasks as directed by leadership.
Work collaboratively in a team environment, follow Good Manufacturing Practices, adhere to internal policies, participate in training, and maintain organized workspaces.
Qualifications: Not specified.
Salary: To be negotiated.
Position: Systems Analyst
Company: Cifarma
Industry: Pharmaceutical manufacturing, Chemical/Pharmaceutical sector.
Additional Details:
Seniority Level: Entry level
Employment Type: Full-time
Job Function: Information Technology
Industry: Pharmaceutical Manufacturing
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