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QA Validation Officer

BASED: Florence

CONTEXT

The candidate will join QA Validation Group inside Site Quality Assurance and will be in charge of reviewing validation documentation.

MAIN ACTIVITIES AND RESPONSIBILITIES

• Write and review Standard Operating Procedures (SOPs) and Risk Assessments
• Review Validation Protocol/Report for Equipment, Utilities, Software and Informatics Systems
• Write and review Perfomance Qualification Protocol/Report
• Write and Cooperate to manage Validation Master Plan,
• Work with production, engineering, quality control in order to fulfil the Validation Master Plan scheduling
• Support project involving equipment, utilities, Software and Informatics Systems
• Participate in CAPA planning and problem-solving efforts

JOB REQUIREMENTS

• 1- 2 years of experience in pharmaceutical companies/consulting companies;
• Degree in Chemical and Pharmaceutical Technology, Chemistry, Engeneering, Biotechnologies
• Fluent English
• Problem solving
• Great attitude to team work
• Be flexible and precise

 

Degrees of interest: Degree in Chemical and Pharmaceutical Technology, Chemistry, Engeneering, Biotechnologies