compliance & regulatory affairs officer (male/female).

κάνε την αίτησή σου

περιγραφή εργασίας

βασικές πληροφορίες για τη θέση εργασίας

Επιταχύνετε την εφαρμογή εργασίας κοινοποιώντας το προφίλ σας

περιγραφή εργασίας

  • παροχές

    For the Compliance Officer position the company offers competitive salary.

  • κύριες αρμοδιότητες

    • GDP Compliance: Ensure full adherence to Good Distribution Practice (GDP) guidelines, overseeing the proper handling, storage, and distribution of medicines across target markets.
    • Quality & Documentation Management: Maintain up-to-date quality dossiers, standard operating procedures (SOPs), company policies, and compliance documentation.
    • Pharmacovigilance (GPvP): Execute and follow all pharmacovigilance-related SOPs in accordance with Good Pharmacovigilance Practice guidelines.
    • Regulatory Operations: Support regulatory compliance activities to ensure smooth product availability across various markets.
    • Cross-Functional Scope: Manage a versatile range of operational duties covering Quality Assurance, Regulatory Affairs, and Pharmacovigilance.

  • προσόντα

    The qualifications for the Regulatory Affairs Officer position include:

    • Degree in Pharmacy or Life Sciences (e.g., Biology, Chemistry, or related scientific field).
    • Excellent Knowledge of the English language.
    • Good knowledge of Local, EU and International regulatory affairs legislation and guidance.
    • Good written communication skills with attention to detail.
    • Strong critical thinking and ability of data interpretation.

  • εμπειρία

     1–3 years of relevant experience in Quality, Regulatory Affairs, Pharmacovigilance, or Complianc

  • Πληροφορίες

    Does this role sounds like you or someone you know?

    We want to hear from you today. Apply online now!

    Foteini Kirtzali+306948238979Please note that for transparency and equity reasons, only those applications made online via our site will be assessed. After the screening of all the CVs received, we will only contact the candidates who meet the requirements of the job to arrange an interview. ​ All applications are considered strictly confidential.

μοιράσου αυτή τη θέση εργασίας

τα στάδια που θα ακολουθήσουν από την αίτηση σου

Δες τα στάδια που ακολουθούμε μετά την υπολοβολή της αίτησης σου σε μια θέση εργασίας. Μάθε περισσότερα για το πως μπορούμε να σε βοηθήσουμε να κάνεις το επόμενο επαγγελματικό σου βήμα.

επικοινώνησε μαζί μας

είμαστε εδώ για να σε βοηθήσουμε με τυχόν απορίες που μπορεί να έχεις.

Foteini Kirtzali

foteini kirtzali

σχετικές θέσεις εργασίας

εμφάνιση όλων των θέσεων εργασίας

  • clinical study planning manager (male/female)

    • marousi, attica
    • μόνιμη
    On behalf of Merck, a premier global science and technology company, we are seeking a dynamic Clinical Study Planning Manager to oversee and optimize clinical trial operations.Are you an experienced clinical operations professional with a strong background in study planning, budgeting, and operational data management? Do you thrive on translating complex operational data into actionable strategic insights to ensure clinical trials run efficiently, on time,
    δημοσιεύτηκε 22 οκτωβρίου 2026
    On behalf of Merck, a premier global science and technology company, we are seeking a dynamic Clinical Study Planning Manager to oversee and optimize clinical trial operations.Are you an experienced clinical operations professional with a strong background in study planning, budgeting, and operational data management? Do you thrive on translating complex operational data into actionable strategic insights to ensure clinical trials run efficiently, on time,
    εμφάνιση λεπτομερειών θέσης εργασίας

  • clinical data associate (male/female)

    • marousi, attica
    • μόνιμη
    On behalf of Merck, a premier global science and technology company, we are seeking a dedicated Clinical Data Associate to join the Data Monitoring, Management & Innovation (DMMI) team in Maroussi, Greece.Are you a skilled Clinical Data Management professional with 5–7 years of experience in pharma, biotech, or CRO, and hands-on expertise with EDC systems such as Medidata Rave, Oracle InForm, or Veeva? Do you thrive on reviewing, validating, and cleaning c
    δημοσιεύτηκε 22 οκτωβρίου 2026
    On behalf of Merck, a premier global science and technology company, we are seeking a dedicated Clinical Data Associate to join the Data Monitoring, Management & Innovation (DMMI) team in Maroussi, Greece.Are you a skilled Clinical Data Management professional with 5–7 years of experience in pharma, biotech, or CRO, and hands-on expertise with EDC systems such as Medidata Rave, Oracle InForm, or Veeva? Do you thrive on reviewing, validating, and cleaning c
    εμφάνιση λεπτομερειών θέσης εργασίας

  • qa validation officer (male/female)

    • schimatari, attica
    • μόνιμη
    Are you an experienced Quality Assurance professional within the pharmaceutical industry? We are currently looking for a QA Validation Officer on behalf of our client, a well established company in the field of pharmaceutical products.In compliance with pay transparency and equal treatment obligations (Greek Law 5316/2026 & EU Directive 2023/970), the applicable salary range for this position will be communicated to candidates invited for an assessment int
    δημοσιεύτηκε 5 οκτωβρίου 2026
    Are you an experienced Quality Assurance professional within the pharmaceutical industry? We are currently looking for a QA Validation Officer on behalf of our client, a well established company in the field of pharmaceutical products.In compliance with pay transparency and equal treatment obligations (Greek Law 5316/2026 & EU Directive 2023/970), the applicable salary range for this position will be communicated to candidates invited for an assessment int
    εμφάνιση λεπτομερειών θέσης εργασίας

Σε ευχαριστούμε για την εγγραφή σου στις ειδοποιήσεις θέσεων εργασίας.