Quality & Regulatory Project Manager
Location: BelgiumSIRE® 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 Biotechnology organisation, based in Hainaut Belgium.
Ensure compliance and implementation of the standards and regulations
Manage the project team
Keep track of deadlines and deliverables
Maintain contact with the authorities
Minimum 4 years of experience in QA and RA
Thorough background in the pharmaceutical industry
Affinity or interest with immunotherapy
Professional proficiency of French, Dutch and English
People management experience and good organisational skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Nicolas Gyselinck.
The Company
I am approached by a client who is based in Hainaut, Belgium who is a European market leader in biotechnology and biopharmaceuticals. Their products and services are well known amongst a lot of healthcare professionals throughout the world.Role Description
They are currently looking for a new project manager who will manage the Regulatory Affairs team and take control over the Quality Assurance activities. The manager needs to make sure the products are in compliance with both authority regulations and applicable quality standards.Responsibilities
Lead the ongoing and new RA and QA projectsEnsure compliance and implementation of the standards and regulations
Manage the project team
Keep track of deadlines and deliverables
Maintain contact with the authorities
Requirements
MSc in a scientific field, preferably in something relevant such as biochemicalsMinimum 4 years of experience in QA and RA
Thorough background in the pharmaceutical industry
Affinity or interest with immunotherapy
Professional proficiency of French, Dutch and English
People management experience and good organisational skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Nicolas Gyselinck.
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