Teva Site Quality Manager 

Israel, South District, Beer Sheva 

610911478

Join the TAPI Quality organization in an exciting and crucial role as Site Quality Head of Teva-Tech and Plantex sites in Israel. You will lead a team of about 90 colleagues taking care of Quality Assurance, Quality System, Quality Compliance and Quality Control at the sites.. While reporting directly to the VP Quality of TAPI, you will be part of the sites’ Leadership Team, working integrated with its members.

• Lead Quality- Lead the site's Quality team in establishing and maintaining quality at the site in accordance with Teva's global standards, regulatory guidelines and CGXP compliance requirements. Maintain high standards of quality at the site through managing and continuously improving the effectiveness of quality processes and systems.
• Manage Team and Resources- Identify, develop, and retain qualified people to lead the implementation of quality processes. Run an efficient and effective Quality organization through managing the Quality site budget and Quality resources.
• Drive a Sustainable Culture of Quality- Lead the site's Quality team. As an influential member of the site's leadership team, create, develop and maintain a culture of enhancing quality throughout the entire site operation.
• Embed Quality into the Site's Leadership- Ensure Quality is embedded in the management team's decision-making and how they view and drive their site's operational activities
• Independent Authority- Maintain position as an independent and autonomous authority on all quality related decisions.
• Manage Regulatory Relations- Develop productive and proactive relationships with regulatory bodies.
• Coordinate with Quality Leadership- Share best practices, challenges and lessons learned within the site across the Quality organization in order to improve the performance of quality globally.
  

• 10+ years of experience working as Manager in a manufacturing site, with at least 5 years in Quality and/or Compliance, with extensive exposure to site operations.
• Bachelor/Master of Science (Chemistry/Biotechnology/Pharmaceutical Chemistry/Pharmacy) or equivalent
• Advanced knowledge of local GxP requirements as well as international Authorities, including USFDA and EMA
• Adequate experience in Compliance and Health Authority interaction. Working knowledge of audit and inspection management, response writing and CAPA management
• Advanced communication and negotiation skills, strong interpersonal skills, and excellent presentation skills.
• Ability to work with various organizational leadership levels and in a team environment across multiple roles.
• Energetic and committed to continuous improvement to evolving compliance expectations.
• Proactive orientation, self-motivated, flexible, and innovative way of thinking.
• Intercultural sensibility
• Fluency in Hebrew and English
  

Vice President Quality AMSO

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