Senior QA Associate
Location: NetherlandsSIRE® 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.
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
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.
The Company
.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.
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