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Head of Investigations and Improvement

Haarlem, Netherlands

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

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.

How you’ll spend your day

  • 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.

Your experience and qualifications

  • 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

Reports To

Head of Production Teva Haarlem

Contact person

Ivo Huijskens - Senior Recruiter

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Pre Employment Screening

Teva will carry out appropriate verification and legally permitted vetting prior to the confirmation of any offer of employment. More information on this verification and vetting will be provided if you reach this stage of the application process.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Blijf op de hoogte van de laatste farma vacatures


Blijf op de hoogte van de laatste farma vacatures