About the Role:
This position encompasses responsibilities across GxP areas, focusing on GVP and GDP, along with quality assurance involvement in IT operations. As a key member of the QA department, you will:

• Support and foster a well-established culture of quality.
• Contribute to the strategic direction and continuous improvement of the QMS.
• Manage quality assurance responsibilities for client pharmaceutical companies, assuming specific roles as required.

Key Responsibilities:

• Oversee and manage assigned quality assurance areas.
• Develop, review, and update procedural documents within the QMS.
• Handle quality processes, including document control, non-conformity management, vendor qualification and oversight.
• Plan, conduct, and manage internal, vendor, and client audits.
• Manage change control and risk management activities.
• Provide quality assurance support for IT operations, including support for ISO 27001 certification.
• Deliver consultancy and training on quality-related topics.

Key Requirements:
We are seeking candidates who are passionate about quality and conceptually strong in Quality Management, with the following experience:

• At least 3 years of experience in Pharmaceutical Quality Assurance, with expertise in GVP, GDP, or GCP (GMP experience will also be considered), OR
• At least 3 years of experience in Pharmacovigilance or Clinical Development, plus a minimum of 2 years’ experience in full time Quality Assurance roles.

Additionally:

• Knowledge of Drug Safety/Pharmacovigilance is an advantage.
• Fluency in English is required.
• Strong computer skills are essential.

What We Offer:

• Competitive renumeration package
• A professional work environment that values and prioritizes quality.
• Considerable opportunities for professional development.

Due to the critical nature of this role, candidates will undergo testing and personal interviews.

If you're ready to contribute to our exciting growth phase and elevate our HR practices, apply now by submitting your CV to: hr@medwork.gr

All applications will be treated in strict confidentiality.
Only suitable candidates will be contacted.

Με την υποβολή του βιογραφικού σας και τη συμμετοχή σας στην παρούσα διαδικασία αξιολόγησης, μας παρέχετε την ρητή και θετική συναίνεσή σας για την αποθήκευσή των πληροφοριών (προφορικών και γραπτών) που μας παρέχετε (π.χ. βιογραφικό, συμπληρωματικές πληροφορίες, γραπτών τεστ, κ.α.) και την μελλοντική επεξεργασία των προσωπικών σας δεδομένων για τους σκοπούς της αγγελίας, συμπεριλαμβανομένης της επικοινωνίας μαζί σας. Η αποθήκευση των παρεχόμενων πληροφοριών θα έχει μέγιστη διάρκεια 5 ετών. Σε κάθε περίπτωση, διατηρείτε το δικαίωμα της αίτησης για διαγραφή των παρεχόμενων πληροφοριών πριν την παρέλευση του καθορισμένου χρόνου.