Job Description

Lavipharm is seeking a Quality Validation / Qualification Specialist, based in Athens, who will be responsible for compliance to GMP and regulatory requirements of facilities, utilities, equipment and computerized systems.

Responsibilities

• Plan, overview execution, review results and approve qualification and validation activities (DQ, IQ, OQ, PQ)
• Ensure appropriate prioritization of validation activities regarding manufacturing equipment, utilities, facilities and computerized systems
• Issue, review and approve validation protocols, reports and supporting documentation
• Maintain validation status throughout the lifecycle of systems and equipment
• Provide QA oversight for change control, deviations and CAPAs related to validation
• Ensure application of risk-based approaches to validation/qualification activities

Requirements

• Bachelor’s degree preferably in Engineering or Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology or other relevant field
• Postgraduate qualification (master’s degree or equivalent) in a relevant field is preferred
• At least 5 years experience in Quality manufacturing/systems preferably in Human Pharma Industry
• Excellent knowledge of the English language
• Computer Literacy (MS Office etc)