- Regulatory Compliance and Documentation: Maintain up-to-date product dossiers, including applications for new product licenses and formulations to health authorities or supporting customers to the relevant documentation needed, ensuring compliance wi
- Audit Support: Assist with customer and regulatory audits, including preparation and follow-up actions.
- Training: Provide training on assigned procedures.
- Documentation Management: Collaborate with QA to maintain quality policies and manuals.
- CAPA Management: Manage corrective and preventative actions.
- Quality Reporting: Produce quarterly reports on product quality trends.
experience - At least 2-4 years in a Quality Assurance position
qualifications - University degree preferably in Chemistry, Pharmacy, Biology, Chemical Engineer or similar scientific disciplines
- Compliance with requirements that related to the appointment as Qualified Person (QP) in accordance with EU or regional regulations (e.g., article 49 of EU Directive 2001/83/EC) is preferable.
- Excellent Greek and English oral communication and scientific writing skills.
- Competency in Microsoft Office focused to Microsoft word and Microsoft Excel.
- Results-oriented with strong organizational skills, excels in teamwork, and effective at communication internally and externally.
- Ability to work under pressure and problem-solving orientation.
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Περιγραφή
Are you looking to take the next professional step as a QA Compliance Specialist within a well established company? If you're ready to advance your career, we have the perfect opportunity for you.
This QA role aims to enhance our client's QA team and support the company's continuous improvement plan.
key responsibilities
