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Site Quality Head
Site Quality Head-May 2024
Istanbul
May 4, 2025
ABOUT NOVARTIS
At Novartis, we’re reimagining medicine to improve people’s lives through innovative science and technology.
10,000+ employees
Biotechnology
VIEW COMPANY PROFILE >>
About Site Quality Head

  About the Role

  • Ensure that all aspects of the handling, manufacturing, testing, release of products at the site are compliant with GMP, GDP, Corporate Standards and any applicable local/international Regulatory Standards.

  • Staff, train, and develop the quality department

  • Provide leadership, direction and support to the people within the Quality department and ensure that they are qualified, achieve a high level of competence, are motivated and carry out their duties in a safe manner.

  • Co-ordinate with other members of the management's operating team in the day-to-day conduct of the site's business.

  • Develop and implement processes to improve quality, demonstrate ongoing control and cost efficiency.

  • Maintain, along with your team the plant in a validated state.

  • Participate in, respond to all Health Authority, internal and external audits, and be the site responsible for this matter. Be the Quality spokesperson during external audits.

  • Prepare, present and manage the budget for operational expenses, headcount and capital investments

  • Ensure adequate management of product critical quality issues (deviations, out of specifications). Ensure investigations are accurately executed and adequate CAPAs are defined, and accurately follow up of CAPAs efficiency.

  • Define, implement, supervise, consolidate, and analyze Site Quality KPIs. Drive for Site management team accountability.

  Diversity & Inclusion / EEO

  Olağanüstü, dahil edici bir çalışma ortamı sunmak ve hizmet verdiğimiz hastalar ile toplulukları temsil eden çeşitli ekip temsilcileri oluşturmaya kendini adamıştır.

  Role Requirements

  • Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering or related field. (Advanced degree is preferred.)

  • Minimum of 10 years' experience in an operational GxP area, in Manufacturing/Development or Quality.

  • Profound experience leading sophisticated quality organizations in a diverse global matrix environment.

  • Ability to speak up and to take Quality decisions during challenging situation.

  • Strong leadership skills with excellent interpersonal, communication and negotiation abilities. With confirmed experience in change management and integration of teams and/or organizations.

  • Expertise in organization dynamics and culture, ability to gain trust and confidence at all levels in the organization, leadership and project management experience.

  • Ability to work independently and effectively in international, complex and multifaceted environments.

  • Advanced level of writing/speaking skills in English.

  Division

  Operations

  Business Unit

  QUALITY

  Location

  Turkey

  Site

  İstanbul

  Company / Legal Entity

  Novartis Turkey

  Job Type

  Tam Zamanlı

  Employment Type

  Daimi

  Shift Work

  Hayır

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