Teva Associate Director Investigations Improvement 

Netherlands, North Holland, Haarlem 

632589410

Management of the Investigation & Improvement department and broad support of Operations by means of knowledge contribution, development and realization of improvement processes (by CAPA and Change control), co-realization of pharmaceutical production, challenging production processes, performing investigations (gDR) and analyzing batch documentation and batch review, in such a way that an optimal working method and product quality are guaranteed in the production process. You will manage a team of 7 professionals, 3 project managers and 4 pharmaceutical specialists.

• Develop, implement, and manage departmental objectives aligned with our annual production plan.
• Provide direction and leadership for the Investigation & Improvement (I&I) 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.

• 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

Ivo Huijskens - Senior Recruiter

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