πριν από 5 μέρες
source :

Περιγραφή Θέσης

DEMO S.A. Pharmaceutical Industry is an industrial and commercial organization established in 1965 and active in the production and sales of pharmaceutical products.

DEMO S.A. is ranking first among all the Greek pharmaceutical companies in terms of units sold. Our product portfolio includes many injectable generic pharmaceutical formulations from several therapeutic categories.

In the private market the company's portfolio consists of prescription general medicine, cardiology, pulmonology, oncology, pathology, urology products and medical devices.

DEMO S.A. has a long history of successful participation in international tenders procured by the most accredited organizations worldwide to Europe, Asia, Africa, the Middle East, South America and Oceania.

The company exports 81% of its annual output and is rapidly expanding its product range to international markets along with timely and secures delivery.

Our company is registered supplier for numerous international organizations, including the UN, UNICEF, WHO, MSF et al. With over 2,000 approved products in 85 countries and over 900 staff our goal is to be consistently one of the best companies in the pharmaceutical market, maintaining our leadership position in the Greek industry and internationally.

DEMO S.A. is one of the 10 most attractive employers in Greece based on Randstad's Employer Brand Research for 2019.

In this context, we are seeking to hire highly motivated professionals to cover the following position :


Main duties and responsibilities :

  • Develops and implements the required monitoring procedures with all external manufacturing partners for finished dosage forms.
  • Supports the strategic planning and execution of External Manufacturing & Supply operations related with DEMO’s external manufacturing partners and suppliers.
  • Responsible for design and execution of the technical transfer process into all CMOs (Contract Manufacturing Organizations) for all products.
  • Pre- and post-launch support.
  • Delivers timely project management and execution of Technical Transfer projects for existing and new product launches.
  • Leads external manufacturing and sourcing in a cost-efficient manner.
  • Supports the Purchasing, Quality and Regulatory departments by providing technical solutions for CMO supply & quality issues.
  • Manages changes in the supply chain.
  • Experience, skills and qualifications required :

  • Bachelor’s degree in Life Sciences required, Master’s degree is preferred.
  • 3 - 4 years of related experience in product supply and external manufacturing in the Pharmaceutical industry.
  • Ability to make decisions in design, management and execution of external manufacturing alliances.
  • Expert in Microsoft Office (Excel, PowerPoint, Word)
  • Strong communication skills and ability to work cross-functionally.
  • Results-driven with a high level of commercial awareness and business acumen.
  • Leadership skills and ability to communicate with people of all levels.
  • Solid understanding of the generic drug development process and GMP requirements.
  • Τ he Company offers the competitive remuneration, continuous education and training, the potential for professional development, and an excellent work environment.

    All applications will be considered as strictly confidential. Please send your CV with Reference code : BDSC 05 / 20.

    Αναφορά αυτής της εργασίας

    Thank you for reporting this job!

    Your feedback will help us improve the quality of our services.

    Υποβάλετε αίτηση
    Το e-mail μου
    Πατώντας στο κουμπί «Συνέχεια », δίνω στο neuvoo τη συγκατάθεση μου να καταχωρήσει τα δεδομένα μου και να μου στέλνει ειδοποιήσεις μέσω email, όπως αναφέρεται λεπτομερώς στην πολιτική προστασίας προσωπικών δεδομένων του neuvoo. Μπορείτε ανά πάσα στιγμή να αποσύρετε τη συγκατάθεση σας ή να διαγραφθείτε οποιαδήποτε στιγμή.
    Φόρμα αίτησης