Projectmanager Cleanrooms

Projectmanager Cleanrooms Bilzen (HQ), Belgium Voltijds Over de job Als Cleanroom Project Manager ben je betrokken bij het ontwerp, de realisatie en het onderhoud van complexe uitdagingen in laboratoria, ziekenhuizen, biotech & pharma, voeding, onderzoek en hightech bedrijven. Je bent verantwoordelijk voor het beheer, de co?rdinatie en succesvolle afronding van onze Cleanroom projecten in de […]

Business Development Manager Germany

Business Development Manager Germany (English) Germany Fulltime Job description As Business Development Manager Germany, you will be responsible for ABN Cleanroom Technology?s development in the German area. Since its foundation, ABN Cleanroom Technology has been committed to developing innovative cleanroom concepts where modularity and pre-engineering are key values. With this innovative approach, we consistently deliver […]

ABN Cleanroom Technology invests in antibody production

Limburg-based companies ABN Cleanroom Technology and simAbs are joining forces to make great strides together within the Life Sciences sector. ABN Cleanroom Technology will provide simAbs, which is currently housed at Bioville Health Campus, with a cGMP-certified cleanroom that meets all requirements to run their operations and increase their production capacity.

DryCell – The first ready to use low dewpoint cleanroom solution in EU

With the increasing demand for electronic devices and electric vehicles throughout the world, more and more manufacturers are running into the same problem: the supply of components, especially batteries, is not keeping up with the massive demand. To meet overall demand in time, additional facilities for production of lithium-ion batteries should be built in the short-term. Battery cell production is a mission critical challenge because the materials used in lithium-ion batteries react heavily with humidity. For that reason, we introduced DryCell.

Digitizing GMP validation processes

A company?s records are a prized possession and should be taken care of the best way possible. When we think of?good manufacturing practices (GMP), regulations must be followed to keep the quality and integrity of these records in good standing.?Records are official evidence proving that certain tasks have been completed as they should be ?evidence of compliance? and poorly documenting can negatively impact cleanroom process quality. In this article, we?ll shortly discuss paper records vs. electronic records for GMP processes.

1. Off-site production, on-site assembling

Legolisation means standardisation. Standardisation causes a shift in production. Work is carried out in conditioned spaces such as factory halls. our cleanrooms are manufactured partly or entirely off-site, which means huge savings on transport costs and reduction of inconvenience on-site