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 organisation, based in Netherlands.

The Company

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Role Description

this is a role for an experienced QA professional who likes to keep on learning, be involved in many activities simultaneously and has a proven project management track record.

Responsibilities

Providing QA advice and oversight to different kinds of projects related to investigational products;
Managing quality processes to maintain and improve our internal Quality Management System in order to ensure GXP compliance;
Contractor management
Assessment of GXP-related activities

Requirements

You have a master degree in biosciences or a degree in pharmacy;
You have at least 8 years of QA experience in GMP/GCP within (bio)pharma;
You have experience in developing quality systems and auditing GXP contractors;
You are quality and compliance driven, eager to learn and you have strong analytical skills;
You are fluent in English (both written as well as spoken);
Knowledge of the German Language is a plus;
Willingness to travel up to 15% of the time

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