Director of Investigations and Quality Improvement

5 uur geleden

Haarlem, Noord-Holland, Nederland Teva Pharmaceuticals Voltijd

About the Opportunity

Teva Pharmaceuticals is seeking a highly experienced and skilled professional to lead our Investigation and Improvement department. As Associate Director, you will be responsible for managing a team of 7 professionals, 3 project managers, and 4 pharmaceutical specialists. Your primary focus will be on ensuring the optimal working method and product quality in our production process.

Key Responsibilities

  • Develop, implement, and manage departmental objectives aligned with our annual production plan.
  • Provide direction and leadership for the Investigation and Improvement team, fostering a culture of continuous improvement.
  • Plan, prioritize, and oversee departmental activities, ensuring efficient execution and alignment with broader operational goals.
  • Collaborate effectively with cross-functional teams (QA, RA, etc.) to identify and address production challenges.
  • Manage and mentor a team of 9 consisting out of Project Professionals and Pharmaceutical Specialists, guiding their development and ensuring a high-performing team environment.
  • Lead investigations into production deviations, implementing corrective actions (CAPA) 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.

Requirements

  • 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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