Quality Validation / Qualification Specialist

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

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)