Qualified Person - Leiden

Function Group: Quality/RA / QP


Operating around the world with offices in Australia, Canada, Germany, Japan, the Netherlands, Sweden, United Kingdom, and the United States, this state of the art consultancy firm provides clients with a comprehensive suite of global support. This organisation is in the top 10 fastest-growing privately owned life science consultancy companies. The office based in Leiden with 100 colleagues, is serving its clients with regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Since they are working together with highly skilled employees, they are very successful in building long-term relationships with clients by providing leading industry knowledge, experience, and proven processes. This fast-growing company has close to 700 clients worldwide, 1100+ colleagues from engineers to pharmacists, and is supporting her clients in six continents. For the office in the Netherlands, based in Leiden we are looking for a Qualified Person (QP) with several years of experience.


Are you interested in an independent, responsible and consulting role in a fast-growing organisation with possibilities to (further) develop yourself as a QP? This might be your chance! You will work for several clients on projects with a duration between one month and two years. With a strong and committed client-base throughout the country, the organisation is able to provide you with lots of opportunities that will maintain an excellent work-life balance. You will be working for large multinational pharma companies till very promising start/scale-ups. You will help those companies with a very wide variety of services, such as setting up manufacturing, batch releases, request for licenses and QA support. In this role, it is important that you are able to have effective communications with clients and that you can work autonomously on projects. It goes with saying that you have over a thousand colleagues that will have your back and support you. Because when you are working at you a client, the client actually hires the knowledge of over a thousand international consultants.


We are preferably looking for someone with experience with multiple formulations. In this role, it is important that you are results and clients orientated and that you are a powerful communicator. It is important that you feel comfortable working on deadlines and that you are feeling at home in a fast-changing environment. We are looking for someone that sees it as a challenge to solve issues in a pragmatic and proactive way. Furthermore:

  • At least seven years experience in GMP related areas in QA and/or QC in the life science industry
  • At least one year experience as a QP
  • Good understanding of GMP and European regulations
  • Experience in Biologicals is a plus
  • Experience in clinical trials is a plus
  • Proficient in both Dutch and English


  • Salary starting at 70.000 a year
  • Company car
  • Pension scheme
  • Great secondary benefits
  • Great diversity in the content of the work
  • Working in a fast-growing and professional organisation
  • An environment, which strives for high quality, continuous improvement, and knowledge sharing


If you are interested in this job, or in similar ones, please feel free to contact me directly.

Stijn Koehler
Senior Consultant Biotech/Pharma


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