QC - Compliance Officer
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 Pharmaceutical, Chemicals, Biotechnology and Clinical Research organisation, based in Oost-Vlaanderen Belgium.
You will be actively contributing to establish and implementate the lab compliance and related CAPAs resulted from internal and external (audit) observations including:
-Investigate the audit observation or adverse event
-Define and discuss CAPA proposals with CAPA owners and the managers of the different labs
-Keep track of CAPAs until closure
You are fluent in Dutch and English (spoken/written)
We offer you specialized technical training, challenging mobility prospects and personal development opportunities.
A competitive salary package including extra holidays, hospitalization insurance, company restaurant, pension plan, bonus scheme.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ewout de Jong.
The Company
An ambitious, no-nonsense working environment at one of the leading companies in the chemical industry.Role Description
You will be maintaining, optimizing and further developing the company's global management system (GMS) related to all lab activities. Make adequate analyses of analytical business processes reflected in SOPs procedures and current guidelines. Improve existing SOPs and procedures through making them more clean and understandable for the different analytical labs.Responsibilities
You are the representative of analytical cross-functional compliance teams where you stay connected with compliance colleagues from other departments to make sure the overal approach is aligned and throughout the entire company.You will be actively contributing to establish and implementate the lab compliance and related CAPAs resulted from internal and external (audit) observations including:
-Investigate the audit observation or adverse event
-Define and discuss CAPA proposals with CAPA owners and the managers of the different labs
-Keep track of CAPAs until closure
Requirements
You are in the possession of a master degree and you are familiar with environments preferably in the pharma for a minimum of three years.You are fluent in Dutch and English (spoken/written)
Other information
An ambitious, no-nonsense working environment at one of the leading companies in the chemical industry.We offer you specialized technical training, challenging mobility prospects and personal development opportunities.
A competitive salary package including extra holidays, hospitalization insurance, company restaurant, pension plan, bonus scheme.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ewout de Jong.
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