Senior Director, Pharmaceutical Operations and Quality
4 weken geleden
About the Role
As Senior Director, Pharmaceutical Operations and Quality at Teva Pharmaceuticals, you will lead the Investigation & Improvement department and contribute to the success of our Operations team. Your expertise will drive the development and realization of improvement processes, ensuring optimal working methods and product quality in our production process. You will manage a team of professionals, project managers, and pharmaceutical specialists, fostering a culture of continuous improvement and excellence.
Key Responsibilities
- Develop and implement departmental objectives aligned with our annual production plan.
- Provide leadership and direction for the Investigation & Improvement team, promoting a culture of continuous improvement and quality.
- Plan, prioritize, and oversee departmental activities, ensuring efficient execution and alignment with broader operational goals.
- Collaborate with cross-functional teams to identify and address production challenges, ensuring compliance with Good Manufacturing Practices (GMP) and regulatory requirements.
- Manage and mentor a team of professionals, guiding their development and ensuring a high-performing team environment.
- Lead investigations into production deviations, implementing corrective actions to prevent recurrence.
- Champion a data-driven approach, analyzing processes and identifying opportunities for improvement.
- Participate in and prepare for inspections and audits by national and international authorities, ensuring departmental expertise is represented.
- Report on departmental progress and performance to senior leadership.
About You
- Master's degree in a relevant field (e.g., Pharmaceutical Science or Pharmacy) preferred. Candidates with a Bachelor's degree and significant proven experience will also be considered.
- Extensive experience in managing and leading a production-focused investigation and improvement team within the pharmaceutical industry.
- Proven track record of successfully implementing process improvements that enhance efficiency and product quality.
- Strong understanding of Good Manufacturing Practices (GMP) and regulatory requirements.
- Excellent analytical and problem-solving skills with a focus on root cause analysis.
- Exceptional communication, collaboration, and leadership abilities with a coaching approach.
- A passion for quality, continuous improvement, and building high-performing teams.
- Demonstrated ability to apply scientific judgment to analyze data, solve problems, and make informed decisions in a pharmaceutical context.
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