SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Zuid-Holland Netherlands.

The Company

Their mission is to transform individual lives and fundamentally change the way diseases are interpreted, managed and in the end prevented. In over 150 countries the company is bringing innovative science and together with the most creative minds in the industry think differently about diseases. Trying to achieve the best possible results for their health.

Improving the access to medicines, making the best available treatment at an affordable price, starting in this entrepreneurial company will enrich your career!

Role Description

This team has a strong focus on developing novel therapeutics and vaccines, treating, cure and preventing some of the worlds most devastating infectious diseases. With a broad range of different medicines this team has the drive to seek the best possible way to positively impact the lives of patients.

You will be responsible for the external manufacturing of drug product. Involved in all GMP-related activities for preparation, execution and follow-up actions of asepctic drug product manufacturing at the external Drug Product Manufacturing sites. Working closely together with different project teams.

Responsibilities

- Ensuring and maintaining the quality level
- Inspection readiness, facilitating audits and inspections
- Continuous improvement of procedures
- Being the key user in the companies documentation and quality system
- Organizing drug product distribution to different storage's and clinical facilities
- Maintaining training strategy for the department
- oversight of purchase orders and facilitating the invoicing process

Requirements

- Bachelor or Master in pharmaceutical sciences or similar
- 4 years' of experience in Quality Assurance or Aseptic Drug Product Manufacturing
- Experience in the (bio-) pharmaceutical industry
- Fluent in English, Dutch is a plus
- Pro-active and a strong quality mindset

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Helene de Vries.