QC ANALYST Brussels
SIRE Life Sciences®
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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 Pharmaceutical and Biotechnology organisation, based in Brussels Hoofdstedelijk Gewest Belgium.
The CompanyOur client in Brussels has been producing small and large scale cGMP API peptides for customers in the pharmaceutical and biotechnological field. There expertise is internationally recognized. Thanks to its know-how and capabilities in the field of production technologies and adapts the way it produces to provide its customers with the most efficient production process possible.
They developed there own portfolio of innovative technologies with the aim of improving synthesis processes, controlling quality and simplifying (or eliminating) HPLC purifications for short peptides.
Role DescriptionThe purpose of the function is to carry out physicochemical analysis activities in the quality control laboratory.
The QC laboratory is in charge of testing raw materials, in-process, intermediate and finished products to ensure that they meet the requirements of the Pharmacopoeia and / or Specifications.
The GMP rules are applicable to all tasks related to the quality control team. Compliance with procedures and safety rules are obligations for all QC personnel in all facilities.
ResponsibilitiesFinished product analyzes and stability tests
Participation in the validation of analytical methods
Monitoring of raw materials to intermediaries
Monitoring of work in progress
Stability of intermediaries
Raw material revalidations
Controls cleanings of installations
Maintenance of the most complex QC equipment (Toc, ...)
RequirementsRequired training: Graduate in chemistry / biochemistry (bachelor's degree) or equivalent by experience.
Practical knowledge of physico-chemical analysis techniques (essential HPLC & GC, Titration, ...)
Knowledge in microbiology is a plus.
Proven professional experience in GMP analysis laboratory is essential.
Flexibility: work in 2 shifts (6-14h, 14-22h)
Sense of organization and planning
Rigor and attention to detail
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.