SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!
The companyOur client is a professional Clinical Research and Pharmaceutical organization, based in Brabant Flamand Belgium. They are an independent specialist which offer flexible total packages targeting the quality of design, operation of critical systems, processes and services in regulated environments with as a thread product and patient safety. The company is ISO9001 certified for all its activities. Their services are based on tree pillars: Project support, testing and consulting.
Role descriptionCurrently we are looking for a independent specialist who can provide project support for pharmaceutical and medical organizations. The company supports the customer in the realization and validation (testing) of pharmaceutical manufacturing processes, lab applications, cleanrooms, operating quarters, warehouses and buildings, with the quality and safety of the patient being central. They provide a thorough training by experts in tune with your ambitions, challenging projects and a young and dynamic team with a lot of future opportunities. They are an open organization with a no-nonsense mentality and organize company events on a monthly base. This project will last at least 1 year.
ResponsibilitiesYou will be responsible for the organization and performance of projects from scratch, keep in touch with the contacts of the clients and control all the risk’s in a pro-active way. You will get training about International legislation, guidelines and evolutions in the sector by means of conferences, seminars, internal and external benchmarking and literature studies.
- Advice about cGMP-aspects
- Guide parties who are involved in the development and performance of the project
- Translation of problem statement to achievable plan
Requirements- BSc/MSc within the Pharmaceuticals or Clinical Research
- +- 3 years of related work experience
- Analytical mind
- Critical attitude
- Fluent in Dutch and English with excellent communication skills