Quality Director, Greece

Λεπτομέρειες ρόλου

Quality Director, Greece

Role: Full-time, permanent

Location: Schimatari, Greece

Ο ρόλος

We’re seeking a charismatic and experienced Quality Director to Provide leadership and direction for Quality function and activities at Schimitari, Greece, whilst ensuring compliance to regulatory standards across the Quality function.

Your responsibilities will include:

• You’ll lead and manage the strategic and operational performance of the Quality department, ensuring the successful delivery of business strategy, Key Performance Indicators (KPIs) and objectives, whilst adhering to regulatory compliance and achieving commercial success.
• To manage and develop the site wide electronic Quality System, with a focus on continuous improvement and ensure that all Quality matters are reported on.
• To work with the wider business functions, providing Quality input where required. Across the sites and affiliates.
• Driving forward a Quality first culture, ensuring site wide compliance against all regulations including GMP and implement a training programme
• To provide support for the Quality teams at Accord sites to ensure that EU cGMDP, corporate quality requirements and any other relevant Competent Authority requirements are maintained to support current and future business requirements
• To provide support the development, leadership and implementation of the Quality strategy for the EMENA region
• To provide strategic direction and leadership for the quality teams on site manufacturing facilities, and the Supplier Quality function ,Regional Audit function  and Good Distribution  Practice function
• To ensure that current and future EU/US GMDP requirements are met and that an effective Pharmaceutical Quality system is maintained for the Schimitari site and the Supplier Quality
• To work closely with the EMENA Quality Leadership Team
• To drive improvements and simplification of the Pharmaceutical Quality System
• To provide strategic direction and leadership for the quality teams at Schimitari to ensure that EU cGMDP
• To act as the primary interface with Competent Authorities for GMDP Inspections and for quality related issues under the areas of responsibility
• Responsible for the Quality budget at the Schimitari site and the Supplier Quality Function, and to ensure that appropriate resource within the quality function is available to meet business and regulatory requirements
• To identify and manage Quality risks to minimise patient and business risk due to quality failures
• Accountable for providing Senior Managers with information and data (including recommendations) on the performance of the Pharmaceutical Quality System to drive continuous improvement in quality

Ο Υποψήφιος

• working to EU and US Experience of leading multi skilled teams across multiple sites
• An understanding of oral solid dose and sterile manufacture and related product transfers / new product introductions
• Experience of hosting Competent Authority GMDP Inspections
• A decisive thinker and able to progress actions to a schedule
• A practical approach to developing and implementing procedures and processes within a regulated environment
• Able to work within a global matrix organisation and realise a global quality strategy
• An excellent communicator, who can interact effectively on a global level
• Degree in science discipline
• QP Qualified and previous experience as a QP in Pharmaceutical environment
• Experience in a Quality leadership role, ideally within the pharmaceutical sector or similar.
• Experience of managing high performing teams.
• Responsibility for cost centre management and identifying opportunities for savings and efficiencies.
• Excellent understanding of S&OP.
• Knowledge of Quality management/forecasting tools.

Οι ανταμοιβές

In return, we offer a competitive salary and rewards package. Not to mention the opportunity to genuinely make a difference in a new and dynamic role within a progressive and expanding business, at an exciting time of growing international reach.

Τρόπος υποβολής αίτησης

If you have the experience, passion and ability to make this role a success then we would love to hear from you. Please complete your Candidate Profile on our careers site to apply for this role. The closing date is 31/05/2025. For more information, you can contact us on: careers@accord-healthcare.com

Λίγα λόγια για εμάς

Accord Healthcare Europe is one of the fastest growing pharmaceutical companies in Europe. Accord has one of the largest market footprints of any European generic and biosimilars companies selling generic medicines in over 80 countries around the world. This global footprint enables us to deliver vital, affordable medicines to national health systems supporting healthcare professionals to transform patient lives worldwide. The approach of Accord is agile and inventive, always seeking to improve products and patients' access to them. Accord are driven to think differently and deliver more for the benefit of patients worldwide. To continue our growth, we’re looking for the best and brightest technical minds and forward-thinking business professionals. Keeping our people at the heart of all we do, we offer rewarding opportunities for those looking for continued personal and professional growth, investing in training and development tailored to each individual’s focus. So, if you’re looking for an inclusive company to take your career to the next level, you’re certainly in the right place.  Come and join us to make it better.

Υποσέλιδο

Όλοι οι υποψήφιοι αξιολογούνται  ανεξαρτήτως  φυλής,  χρώματος, θρησκείας,  φύλου, σεξουαλικού προσανατολισμού,  ταυτότητας φύλου, εθνικής καταγωγής ή  ειδικών αναγκών.

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