Job Description
Objective of the role: To qualify and validate all the production and laboratory processes and facilities according to the standard procedures especially validating the computer systems. . List of responsibilities: - Preparing the required protocols to qualify and validate the computer systems; - Running the qualification and validation process of the computer systems and preparing the required reports; - Investigating the computer systems performance on a regular basis; . Reporting to: Qualification & Validation Supervisor. Length of Probation Period: 3 months. Working hours: Saturday to Wednesday 7 a.m to 4 p.m .
Requirements
University Qualifications: Computer engineering (preferably hardware), IT . Specialist knowledge: - Good knowledge of computer software and hardware; - Familiarity with pharmaceutical industry and the relevant standards is a plus; - Familiar with quality assurance processes and procedures; - Fluent in English language; - Good command of MS Office; . Soft Skills and Personality traits: - Highly motivated and active to learn new things; - Interested in the field of quality assurance; - Good at team work; - Result oriented; - Highly resilient; - Continuous learning; - Interpersonal skills;
Employment Type
- Full Time
Seniority
Details
Employment type
- Full Time
Educations
Seniority
