Main duties and responsibilities:
- Supports operations and quality control staff to address compliance related concerns
- Contributes to the establishment, maintenance, continuous improvement and effectiveness of the Quality Management System (QMS), ensuring compliance with current Good Manufacturing Practices (cGMP), internal quality standards and applicable regulatory requirement.
- Identify needs for creation or revision written procedures or revision of existing
- Conducts deviation investigations arising from manufacturing and quality processes, maintains associated records, and ensures appropriate communication and distribution of documentation to affected departments and customers, where applicable
- Reviews and evaluates Change Controls related to manufacturing and quality systems, maintains the associated documentation, and ensures appropriate communication to relevant stakeholders and customers
- Implements and monitors the progress of the Corrective and Preventive Action Plan resulting from findings/observations of Audits from customers/ organizations/authorities
- Prepares validation protocols and reports for process validation.
- Coordinates the preparation, maintenance, revision, control, and distribution of Master Production Documents
Requirements
- BSc Degree in Chemical Engineering, Chemistry or Pharmacy. MSc Degree in Quality Management or relevant field will be considered an asset.
- Previous Experience of at least 2 years in Pharmaceutical Industry
- Fluent oral and written skills in Greek & English
- Computer literacy
- Self-motivated & results oriented with ability to cope with strict timelines
- Ability to deliver on complex project requirements and tasks
- Ability to work creatively, analytically with attention to detail
Benefits
The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment.